Personal authentication apparatus system and method

Information

  • Patent Grant
  • 11741771
  • Patent Number
    11,741,771
  • Date Filed
    Friday, September 24, 2021
    2 years ago
  • Date Issued
    Tuesday, August 29, 2023
    8 months ago
Abstract
A target authentication device includes an electrode to detect an electrical signal associated with a user of the device. The electrical signal represents an authentication code for the device. An authentication receiver module is coupled to the electrode. The module receives the electrical signal from the electrode and determines whether the electrical signal matches a predetermined criterion to authenticate the identity of the user based on the electrical signal. An authentication module is also disclosed. The authentication module includes one electrode to couple an electrical signal associated with a user to a user of a target authentication device, the electrical signal represents an authentication code for the device. An authentication transmission module is coupled to the electrode. The authentication transmission module transmits the electrical signal from the electrode. A method of authenticating the identity of a user of a target authentication device also is disclosed.
Description
INTRODUCTION

The present disclosure is related generally to authentication and/or passing value tokens, the process of confirming the identity of a person by verifying the validity of at least one form of identification by a target authentication device. More particularly, the present disclosure is related to employing personal authentication techniques to authenticate users of the target authentication device.


Conventional modes of authentication include the use of passwords generally composed of character strings composed of letters (a, b, c, . . . ), numbers (1, 2, 3, . . . ), and/or symbols (!, @, #, . . . ) arranged in various combinations.


A minimum level of security for accessing a target authentication device such as a mobile phone is achieved by requiring the owner/user of the mobile phone to enter a unique four-digit character string referred to generally as a Personal Identification Code (PIN), and a passcode in the case of the iPhone brand of mobile phones. The amount of time a mobile phone allows access before requiring re-entry of the PIN is configurable depending on the desired level of security of the owner. Entering a PIN/passcode, however, is a frequent burden for the owner. The owner may be required to enter a PIN/passcode several times per hour throughout the day, every day. In addition to being burdensome for the user, such minimum levels of security are easily hacked by someone skilled in exploiting weaknesses of computer systems.


More generally, however, ways in which someone may be authenticated fall into three categories, based on what are known as the factors of authentication: something the user knows, something the user has, and something the user is. Each authentication factor covers a range of elements used to authenticate or verify a person's identity prior to being granted access, approving a transaction request, signing a document or other work product, granting authority to others, and establishing a chain of authority. For a positive authentication, elements from at least two, and preferably all three, factors should be verified. The three factors (classes) and some of elements of each factor are: the ownership factors: Something the user has (e.g., wrist band, ID card, security token, software token, phone, or cell phone) the knowledge factors: Something the user knows (e.g., a password, pass phrase, or personal identification number (PIN), challenge response (the user must answer a question), pattern) the inherence factors: Something the user is or does (e.g., fingerprint, retinal pattern, DNA sequence (there are assorted definitions of what is sufficient), signature, face, voice, unique bio-electric signals, or other biometric identifier).


Two-factor authentication is when elements representing two factors are required for authentication, the term two-factor authentication is applied—e.g., a bankcard (something the user has) and a PIN (something the user knows). Business networks may require users to provide a password (knowledge factor) and a pseudorandom number from a security token (ownership factor). Access to a very-high-security system might require a mantrap screening of height, weight, facial, and fingerprint checks (several inherence factor elements) plus a PIN and a day code (knowledge factor elements), but this is still a two-factor authentication.


Conventional modes of authentication have become increasingly burdensome and inadequate means for security. Accordingly, new authentication approaches that are robust and less burdensome are needed.


SUMMARY

In one aspect, a target authentication device is provided. The target authentication device comprises at least one electrode configured to detect an electrical signal associated with a user of the target authentication device. The electrical signal represents an authentication code for the target authentication device. An authentication receiver module is coupled to the at least one electrode. The authentication receiver module is configured to receive the electrical signal from the at least one electrode and to determine whether the electrical signal matches a predetermined criteria to authenticate the identity of the user based on the electrical signal.


In another aspect, an authentication module is provided. The authentication module comprises at least one electrode configured to couple an electrical signal associated with a user to a user of a target authentication device, the electrical signal represents an authentication code for the target authentication device. An authentication transmission module is coupled to the at least one electrode. The authentication transmission module is configured to transmit the electrical signal from the at least one electrode.


In yet another aspect, a method of authenticating the identity of a user of a target authentication device is provided. According to the method, at least one electrode detects an electrical signal associated with a user of the target authentication device, the electrical signal representing an authentication code for the target authentication device. An authentication receiver module coupled to the at least one electrode receives the electrical signal from the at least one electrode. A processor determines whether the electrical signal matches a predetermined criterion to authenticate the identity of the user based on the electrical signal.





FIGURES


FIG. 1 illustrates a subject using a mobile device comprising electrodes for detecting personal electrical signals from the body of the subject.



FIG. 2 illustrates one aspect of a mobile device comprising electrodes for detecting electrical signals that can be employed to authenticate the identity of the subject to enable the subject to get access to the mobile device.



FIG. 3 is system diagram of one aspect of a mobile device configured to detect electrical signals for authenticating the identity of the subject.



FIG. 4 is a block functional diagram of one aspect of an authentication subsystem for detecting and/or generating a transconductance signal to confirm the identity of a person.



FIG. 5 illustrates one aspect of an ingestible event marker system configured to generate a unique transconductance signal for confirming the identity of a person.



FIG. 6 illustrates one aspect of an authentication system comprising a target authentication device and an authentication module comprising a body-associated device.



FIG. 7 illustrates one aspect of an authentication system comprising a target authentication device and an authentication transmission module comprising an implantable body-associated device that is located below the skin of the subject.



FIG. 8 illustrates one aspect of an authentication system comprising a target authentication device and an authentication transmission module comprising and an event marker system.



FIG. 9 is a block diagram representation of one aspect of the event indicator system with dissimilar metals positioned on opposite ends.



FIG. 10 is a block diagram representation of another aspect of the event indicator system with dissimilar metals positioned on the same end and separated by a non-conducting material.



FIG. 11 shows ionic transfer or the current path through a conducting fluid when the event indicator system of FIG. 9 is in contact with conducting liquid and in an active state.



FIG. 11A shows an exploded view of the surface of dissimilar materials of FIG. 11.



FIG. 11B shows the event indicator system of FIG. 11 with a pH sensor unit.



FIG. 12 is a block diagram illustration of one aspect of the control device used in the system of FIGS. 9 and 4**.



FIG. 13 is a functional block diagram of a demodulation circuit that performs coherent demodulation that may be present in a receiver, according to one aspect.



FIG. 14 illustrates a functional block diagram for a beacon module within a receiver, according to one aspect.



FIG. 15 is a block diagram of the different functional modules that may be present in a receiver, according to one aspect.



FIG. 16 is a block diagram of a receiver, according to one aspect.



FIG. 17 provides a block diagram of a high frequency signal chain in a receiver, according to one aspect.



FIG. 18A provides a diagram of how a system that includes a signal receiver and an ingestible event marker may be employed, according to one aspect.



FIG. 18B provides a pharmaceutical delivery system that receives control information form a receiver and control the dosage delivery.



FIG. 19 illustrates one aspect of mobile device received in a mating configuration with a mobile device enclosing arrangement comprising a detection circuit integrated therewith for detecting an electrical signal generated by an ingestible event marker.



FIG. 20 illustrates the mobile device and the housing for receiving the mobile device shown in FIG. 19 in an unmated configuration.



FIG. 21 illustrates one aspect of a housing for receiving a mobile device where the housing comprises a detection circuit for detecting an electrical signal generated by an ingestible event marker integrated therewith and a connector for electrically coupling the detection circuit to the functional modules of the mobile device.





DESCRIPTION

Before explaining the various aspects of authentication in detail, it should be noted that the various aspects disclosed herein are not limited in their application or use to the details of construction and arrangement of parts illustrated in the accompanying drawings and description. Rather, any disclosed aspect of authentication may be positioned or incorporated in other aspects of authentication, variations, and modifications thereof, and may be practiced or carried out in various ways. Accordingly, aspects of the authentication apparatus, system, and method disclosed herein are illustrative in nature and are not meant to limit the scope or application thereof. Furthermore, unless otherwise indicated, the terms and expressions employed herein have been chosen for the purpose of describing the aspects for the convenience of the reader and are not to limit the scope thereof. In addition, it should be understood that any one or more of the disclosed aspects, expressions of aspects, and/or examples thereof, can be combined with any one or more of the other disclosed aspects, expressions of aspects, and/or examples thereof, without limitation.


In the following description, like reference characters designate like or corresponding parts throughout the several views. Also, in the following description, it is to be understood that terms such as front, back, inside, outside, top, bottom and the like are words of convenience and are not to be construed as limiting terms. Terminology used herein is not meant to be limiting insofar as devices described herein, or portions thereof, may be attached or utilized in other orientations. The various aspects will be described in more detail with reference to the drawings.


The present disclosure is directed generally to various aspects of authentication by providing a physical connection between a user and a target authentication device. One example of a target authentication device is a computer system. As used herein, the term computer system in intended to encompass a broad category of devices including, without limitation, computer networks, desktop computers, laptop computers, notebook computers, tablet computers, tablet computers, mobile phones, personal digital assistants, appliances, positioning systems, media devices, automatic teller machines (ATM), kiosks, and the like. In addition, authentication is required when entering public modes of transportation (bus, train, subway, airplane, boat, rental car), building entrances, stadiums, turnstiles, and the like. Additional computer systems that may require authentication also may include medical systems that dispense medication in any form.


It will be appreciated that the term “medication” or “dose form” as used throughout this disclosure includes various forms of ingestible, inhalable, injectable, absorbable, or otherwise consumable medicaments and/or carriers therefor such as, for example, pills, capsules, gel caps, placebos, over capsulation carriers or vehicles, herbal, over-the-counter (OTC) substances, supplements, prescription-only medication, ingestible event markers (IEM), and the like.


Prior to describing various aspects of authentication techniques, the present disclosure first turns to FIG. 1 for a brief description of one aspect of a system employing a sensing subsystem coupled to a subject, an event indicator system, and/or a body associated device by way of at least one electrode. A subject can be person or thing that is requesting access to a target authentication device. The body associated device and the event indicator system are configured to generate a unique electrical current signal that is detectable by a detection subsystem. In addition, the detection subsystem may be configured to detect various physiological parameters associated with a living subject.



FIG. 1 illustrates a subject 100 using a mobile device 102 comprising electrodes 104a, 104b for detecting personal electrical signals conducted through the body of the subject 100. In the illustrated example, the mobile device 102 is the target authentication device. The mobile device 102 comprises electrodes 104a, 104b integrated into the housing for detecting electrical signals coupled from the subject 100 to the electrodes 104a, 104b. The term personal electrical signal is used to indicate that a signal is intimately associated with the subject 100 such that it can be used to confirm the identity of the subject 100 for purposes of authentication. Personal electrical signals include, without limitation, physiological signals associated with the subject, transbody conductive signals generated by an ingestible event marker system 106, transbody conductive signals generated by a body-associated device 112, e.g., an adhesive patch that is applied on the body of the subject 100, any object in physical contact with the subject for example watch, bracelet, necklace, ring, etc. and/or transbody conductive signals generated by an implanted body-associated device 113 that is located within the body of the subject 100. Physiological signals include, without limitation, skin impedance, electro cardiogram signals, conductively transmitted current signal, position of wearer, temperature, heart rate, perspiration rate, humidity, altitude/pressure, global positioning system (GPS), proximity, bacteria levels, glucose level, chemical markers, blood oxygen levels, among other physiological and physical parameters. Transbody conductive signals include, without limitation, electrical currents that are transmitted through the body of a subject, where the body acts as the conduction medium. In one aspect, transbody conductive signals can be generated by an ingestible event marker system 106, one example of which is described in connection with FIG. 5. In other aspects, transbody conductive signals can be generated by electrical circuits placed in electrical contact with the surface of the skin of the subject 100 by way of a body-associated device 112. In other aspects, transbody conductive signals can be generated by electrical circuits implanted within the body of the subject 100. Additional aspects of mobile devices 102 configured for detecting an electrical signal from an ingestible event marker system 106, among others, are described in commonly assigned International PCT Application PCT/US/2012/047076, international publication number WO 2013/012869, which is herein incorporated by reference in its entirety.


Regardless of the source, the unique electrical signals suitable for authentication are coupled to the target authentication device, e.g., the mobile device 102, through at least one of the electrodes 104a, 104b, which are suitable for sensing and sourcing electrical signals. In operation, the subject 100 holds the mobile device 102, or otherwise contacts electrodes on another type of computer system, and physically contacts at least one of the electrodes 104a, 104b. The electrical signals are coupled from the subject 100 through at least one of the electrodes 104a, 104b to an authentication subsystem. The authentication subsystem can be integrated with the mobile device 102 or may be added on.


When the ingestible event marker system 106 is the signal source, a unique electrical current signal is generated when the ingestible event marker system 106 contacts digestive fluids 108 in the stomach 110 of the subject 100. The unique electrical current signature is conducted through the body of the subject 100, is detected by at least one of the electrodes 104a, 104b, and is coupled to an authentication subsystem, which decodes the signal and provides a decoded signal to a processing subsystem to authenticate the subject 100.


When the body associated device 112 is the signal source, an electrical current signal is generated by circuits in the body associated device 112. The body associated device 112 is electrically coupled to the body of the subject 100 by another set of electrodes. The electrical signal is conducted by the body and detected by at least one of the input electrodes 104a, 104b on the mobile device 102. These and other aspects of the personal authentication techniques are discussed hereinbelow. Prior to describing such systems, however, the disclosure now turns to measurement subsystems for detecting electrical signals.



FIG. 2 illustrates one aspect of a mobile device 102 comprising electrodes 104a, 104b for detecting personal electrical signals suitable for authenticating the identity of the subject 100. The mobile device 102 also comprises a housing 202, a display 204, an aperture 206 for capturing digital images, and an antenna 208. The electrodes 104a, 104b are located on the back of the housing 202 or at any convenient location of the mobile device 102. In one aspect, for example, the electrodes 104a, 104b may be located on or embedded within a skin or design cover fora mobile device 102 as described hereinbelow in connection with FIGS. 19-21.



FIG. 3 is a diagram of one aspect of a mobile device 102 configured for detecting electrical signals for authenticating the identity of a subject 100. The mobile device 102 may comprise multiple elements. Although FIG. 3 shows a limited number of elements in a certain topology by way of example, it can be appreciated that additional or fewer elements in any suitable topology may be used in the mobile device 102 as desired for a given implementation. Furthermore, any element as described herein may be implemented using hardware, software, or a combination of both, as previously described with reference to node implementations. Aspects of the mobile device 102, however, are not limited in this context.


In various aspects, in addition to a housing 202, a display 204, an aperture 206 for capturing digital images, and an antenna 208, the mobile device 102 comprises a radio subsystem 302 connected via a bus to a processing subsystem 304. The radio subsystem 302 may perform voice and data communications operations using wireless shared media for the mobile device 102. The processing subsystem 304 may execute software for the mobile device 102. A bus may comprise a USB or micro-USB bus and appropriate interfaces, as well as others.


In various aspects, an authentication and/or protection subsystem 306 is coupled to the electrodes 104a, 104b. The electrodes 104a, 104b are configured to be in physical contact with the subject 100 (FIG. 1) to electrically couple the unique electrical signals to and from the authentication subsystem 306. When the subject 100 physically contacts at least one of the electrodes 104a, 104b the authentication subsystem 306 can receive or transmit a unique electrical current signal for authenticating the identity of the subject 100 and, once authenticated, providing access to the mobile device 102. Also, when the authentication subsystem 306 detects physiological signals associated with the subject 100, the authentication subsystem 306 builds a database, which over time provides an average of the physiological signals associated with the subject 100. Authentication occurs only when the detected physiological signals match the running average physiological signals stored in the database.


In various aspects, the detection subsystem 306 is coupled to the processing subsystem 304. The detection subsystem 306 converts the detected electrical signals into a secret word or string of characters. A processing subsystem 304 coupled to the detection subsystem 306 uses the string of characters for user authentication to prove identity of the subject 100 (FIG. 1) or for access approval to gain access to the mobile device 102. When the subject 100 is authenticated, the processing subsystem 304 activates the radio subsystem 304 and other functional modules of the computing device 102, such as, for example, an imaging subsystem 308 or a navigation subsystem 310. When the subject 100 is not authenticated, the processing subsystem 304 denies access to the functional modules of the mobile device 102 until the proper electrical signals are detected by the detection subsystem 306.


In various aspects, the display 204 may comprise any suitable display unit for displaying information appropriate for a mobile device 102. The I/O system may comprise any suitable I/O device for entering information into the mobile device 102. Examples for the I/O system may include an alphanumeric keyboard, a numeric keypad, a touch pad, a capacitive touch screen panel, input keys, buttons, switches, rocker switches, voice recognition device and software, and so forth. The I/O system may comprise a microphone and speaker, for example. Information also may be entered into the mobile device 102 by way of the microphone. Such information may be digitized by a voice recognition device.


In various aspects, the radio subsystem 320 may perform voice and data communications operations using wireless shared media for the mobile device 102. The processing subsystem 304 may execute software for the mobile device 102. A bus may comprise a universal serial bus (USB), micro-USB bus, dataport, and appropriate interfaces, as well as others. In one aspect the radio subsystem 302 may be arranged to communicate voice information and control information over one or more assigned frequency bands of the wireless shared media.


In various aspects, the imaging subsystem 308 processes images captured through the aperture 206. A camera may be coupled (e.g., wired or wirelessly) to the processing subsystem 304 and is configured to output image data (photographic data of a person or thing, e.g., video data, digital still image data) to the processing subsystem 304 and to the display 204. In one aspect, the imaging subsystem 308 may comprise a digital camera implemented as an electronic device used to capture and store images electronically in a digital format. Additionally, in some aspects the digital camera may be capable of recording sound and/or video in addition to still images.


In various aspects, the imaging subsystem 308 may comprise a controller to provide control signals to components of a digital camera, including lens position component, microphone position component, and a flash control module, to provide functionality for the digital camera. In some aspects, the controller may be implemented as, for example, a host processor element of the processing subsystem 304 of the mobile device 102. Alternatively, the imaging controller may be implemented as a separate processor from the host processor.


In various aspects, the imaging subsystem 308 may comprise memory either as an element of the processing subsystem 304 of the mobile device 102 or as a separate element. It is worthy to note that in various aspects some portion or the entire memory may be included on the same integrated circuit as the controller. Alternatively, some portion or the entire memory may be disposed on an integrated circuit or other medium (e.g., hard disk drive) external to the integrated circuit of the controller.


In various aspects, the aperture 206 includes a lens component and a lens position component. The lens component may consist of a photographic or optical lens or arrangement of lenses made of a transparent material such as glass, plastic, acrylic or Plexiglass, for example. In one aspect, the one or more lens elements of the lens component may reproduce an image of an object and allow for zooming in or out on the object by mechanically changing the focal length of the lens elements. In various aspects, a digital zoom may be employed in the imaging subsystem 308 to zoom in or out on an image. In some aspects, the one or more lens elements may be used to focus on different portions of an image by varying the focal length of the lens elements. The desired focus can be obtained with an autofocus feature of the digital imaging subsystem 308 or by manually focusing on the desired portion of the image, for example.


In various aspects, the navigation subsystem 310 supports navigation using the mobile device 102. In various aspects the mobile device 102 may comprise location or position determination capabilities and may employ one or more location determination techniques including, for example, Global Positioning System (GPS) techniques, Cell Global Identity (CGI) techniques, CGI including timing advance (TA) techniques, Enhanced Forward Link Trilateration (EFLT) techniques, Time Difference of Arrival (TDOA) techniques, Angle of Arrival (AOA) techniques, Advanced Forward Link Trilateration (AFTL) techniques, Observed Time Difference of Arrival (OTDOA), Enhanced Observed Time Difference (EOTD) techniques, Assisted GPS (AGPS) techniques, hybrid techniques (e.g., GPS/CGI, AGPS/CGI, GPS/AFTL or AGPS/AFTL for CDMA networks, GPS/EOTD or AGPS/EOTD for GSM/GPRS networks, GPS/OTDOA or AGPS/OTDOA for UMTS networks), among others.


In various aspects, the mobile device 102 may be configured to operate in one or more location determination modes including, for example, a standalone mode, a mobile station (MS) assisted mode, and/or a MS-based mode. In a standalone mode, such as a standalone GPS mode, the mobile device 102 may be configured to determine its position without receiving wireless navigation data from the network, though it may receive certain types of position assist data, such as almanac, ephemeris, and coarse data. In a standalone mode, the mobile device 102 may comprise a local location determination circuit such as a GPS receiver which may be integrated within the housing 202 configured to receive satellite data via the antenna 208 and to calculate a position fix. Local location determination circuit may alternatively comprise a GPS receiver in a second housing separate from the housing 202 but in the vicinity of the mobile device 102 and configured to communicate with the mobile device 102 wirelessly (e.g., via a PAN, such as Bluetooth). When operating in an MS-assisted mode or an MS-based mode, however, the mobile device 102 may be configured to communicate over a radio access network (e.g., UMTS radio access network) with a remote computer (e.g., a location determination entity (LDE), a location proxy server (LPS) and/or a mobile positioning center (MPC), among others).


In various aspects, the mobile device 102 also may comprise a power management subsystem (not shown) to manage power for the mobile device 102, including the radio subsystem 302, the processing subsystem 304, and other elements of the mobile device 102. For example, the power management subsystem may include one or more batteries to provide direct current (DC) power, and one or more alternating current (AC) interfaces to draw power from a standard AC main power supply.


In various aspects, the radio subsystem 302 may include an antenna 208. The antenna 208 may broadcast and receive RF energy over the wireless shared media. Examples for the antenna 208 may include an internal antenna, an omni-directional antenna, a monopole antenna, a dipole antenna, an end fed antenna, a circularly polarized antenna, a micro-strip antenna, a diversity antenna, a dual antenna, an antenna array, a helical antenna, and so forth. The aspects are not limited in this context.


In various aspects, the antenna 208 may be connected to a multiplexer. The multiplexer multiplexes signals from a power amplifier for delivery to the antenna 208. The multiplexer demultiplexes signals received from the antenna for delivery to an RF chipset.


In various aspects, the multiplexer may be connected to a power amplifier, where the power amplifier may be used to amplify any signals to be transmitted over the wireless shared media. The power amplifier may work in all assigned frequency bands, such as four (4) frequency bands in a quad-band system. The power amplifier also may operate in various modulation modes, such as Gaussian Minimum Shift Keying (GMSK) modulation suitable for GSM systems and 8-ary Phase Shift Keying (8-PSK) modulation suitable for EDGE systems.


In various aspects, the power amplifier may be connected to an RF chipset. The RF chipset also may be connected to the multiplexer. In one aspect, the RF chipset may comprise an RF driver and an RF transceiver. The RF chipset performs all of the modulation and direct conversion operations required for GMSK and 8-PSK signal types for quad-band E-GPRS radio. The RF chipset receives analog in-phase (I) and quadrature (Q) signals from a baseband processor, and converts the I/Q signals to an RF signal suitable for amplification by the power amplifier. Similarly, the RF chipset converts the signals received from the wireless shared media via the antenna 208 and the multiplexer to analog I/Q signals to be sent to the baseband processor. Although the RF chipset may use two chips by way of example, it may be appreciated that the RF chipset may be implemented using more or less chips and still fall within the intended scope of the aspects.


In various aspects, the RF chipset may be connected to the baseband processor, where the baseband processor may perform baseband operations for the radio subsystem 514. The baseband processor may comprise both analog and digital baseband sections. The analog baseband section includes I/Q filters, analog-to-digital converters, digital-to-analog converters, audio circuits, and other circuits. The digital baseband section may include one or more encoders, decoders, equalizers/demodulators, GMSK modulators, GPRS ciphers, transceiver controls, automatic frequency control (AFC), automatic gain control (AGC), power amplifier (PA) ramp control, and other circuits.


In various aspects, the baseband processor also may be connected to one or more memory units via a memory bus. In one aspect, for example, the baseband processor may be connected to a flash memory unit and a secure digital (SD) memory unit. The memory units may be removable or non-removable memory. In one aspect, for example, the baseband processor may use approximately 1.6 megabytes of static read-only memory (SRAM) for E-GPRS and other protocol stack needs.


In various aspects, the baseband processor also may be connected to a subscriber identity module (SIM). The baseband processor may have a SIM interface for the SIM, where the SIM may comprise a smart card that encrypts voice and data transmissions and stores data about the specific user so that the user can be identified and authenticated to the network supplying voice or data communications. The SIM also may store data such as personal phone settings specific to the user and phone numbers. The SIM can be removable or non-removable.


In various aspects, the baseband processor may further include various interfaces for communicating with a host processor of the processing subsystem 304. For example, the baseband processor may have one or more universal asynchronous receiver-transmitter (UART) interfaces, one or more control/status lines to the host processor, one or more control/data lines to the host processor, and one or more audio lines to communicate audio signals to an audio subsystem of processing subsystem 514. The aspects are not limited in this context.


In various aspects, the processing subsystem 304 may provide computing or processing operations for the mobile device 102 and/or for the authentication subsystem 306. For example, the processing subsystem 304 may be arranged to execute various software programs for the mobile device 102 as well as several software programs for the authentication subsystem 306. Although the processing subsystem 304 may be used to implement operations for the various aspects as software executed by a processor, it may be appreciated that the operations performed by the processing subsystem 304 also may be implemented using hardware circuits or structures, or a combination of hardware and software, as desired for a particular implementation.


In various aspects, the processing subsystem 304 may include a processor implemented using any processor or logic device, such as a complex instruction set computer (CISC) microprocessor, a reduced instruction set computing (RISC) microprocessor, a very long instruction word (VLIW) microprocessor, a processor implementing a combination of instruction sets, or other processor device. In one aspect, for example, a processor may be implemented as a general purpose processor, such as a processor made by Intel Corporation, Santa Clara, Calif. The processor also may be implemented as a dedicated processor, such as a controller, microcontroller, embedded processor, a digital signal processor (DSP), a network processor, a media processor, an input/output (I/O) processor, a media access control (MAC) processor, a radio baseband processor, a field programmable gate array (FPGA), a programmable logic device (PLD), and so forth.


In one aspect, the processing subsystem 304 may include a memory to connect to the processor. The memory may be implemented using any machine-readable or computer-readable media capable of storing data, including both volatile and non-volatile memory. For example, the memory may include ROM, RAM, DRAM, DDRAM, SDRAM, SRAM, PROM, EPROM, EEPROM, flash memory, polymer memory such as ferroelectric polymer memory, ovonic memory, phase change or ferroelectric memory, silicon-oxide-nitride-oxide-silicon (SONOS) memory, magnetic or optical cards, or any other type of media suitable for storing information. It is worthy to note that some portion or all of the memory may be included on the same integrated circuit as the processor thereby obviating the need for a memory bus. Alternatively some portion or all of the memory may be disposed on an integrated circuit or other medium, for example a hard disk drive, that is external to the integrated circuit of the processor, and the processor may access the memory via a memory bus, for example.


In various aspects, the memory may store one or more software components (e.g., application client modules). A software component may refer to one or more programs, or a portion of a program, used to implement a discrete set of operations. A collection of software components for a given device may be collectively referred to as a software architecture or application framework. A software architecture for the mobile device 102 is described in more detail below.


A software architecture suitable for use with the mobile device 102 may include a user interface (UI) module, an interface module, a data source or backend services module (data source), and a third party API module. An optional LBS module may comprise a user based permission module, a parser module (e.g., National Maritime Electronic Association or NMEA), a location information source module, and a position information source module. In some aspects, some software components may be omitted and others added. Further, operations for some programs may be separated into additional software components, or consolidated into fewer software components, as desired for a given implementation. The mobile device 102 software architecture may comprise several elements, components or modules, collectively referred to herein as a “module.” A module may be implemented as a circuit, an integrated circuit, an application specific integrated circuit (ASIC), an integrated circuit array, a chipset comprising an integrated circuit or an integrated circuit array, a logic circuit, a memory, an element of an integrated circuit array or a chipset, a stacked integrated circuit array, a processor, a digital signal processor, a programmable logic device, code, firmware, software, and any combination thereof.


Having described the mobile device 102 as one example of computer system, it will be appreciated that any of the following computer systems, without limitation, computer networks, desktop computers, laptop computers, notebook computers, tablet computers, tablet computers, mobile phones, personal digital assistants, appliances, positioning systems, media devices, automatic teller machines (ATM), kiosks, public modes of transportation (bus, train, subway, airplane, boat, rental car, . . . ), building entrances, stadiums, turnstiles, medical systems that dispense medication in any form could be equipped with at least one electrode and a detection subsystem to authenticate the user as the owner of the computer system for security purposes. For the sake of conciseness and clarity, not all of these computer systems will be discussed here.


Turning briefly now to FIGS. 19-21, which illustrate aspects of a mobile device 1100 received in a mating configuration with a mobile device enclosing arrangement 1102 comprising a detection circuit integrated therewith for detecting an electrical signal generated by an ingestible event marker, such as the IEM device, otherwise referred to herein as an ingestible event marker system 106, for example. They can be made of hard plastic or in the newer market adhesive-backed vinyl pieces. FIG. 19 illustrates one aspect of a mobile device 1100 received in a mating configuration with a mobile device enclosing arrangement 1102 comprising a detection circuit integrated therewith for detecting an electrical signal generated by an ingestible event marker system 106, for example.


The enclosing arrangement 1102 may be referred to as a housing, enclosure, attachment, skin, design cover, among other accessories for mobile devices, and may substantially or partially cover or enclose the mobile device 1100. FIG. 20 illustrates the mobile device 1100 and the enclosing arrangement 1102 (cradle, protective cover, skin, and the like) for receiving the mobile device 1100 in an unmated configuration. The mobile device 1100 shown in FIGS. 19 and 20 is substantially similar to the mobile devices 102 and others described hereinbefore and, therefore, a high level description of similar functional modules will not be repeated here for the sake of conciseness and clarity of disclosure.


As shown in FIGS. 19 and 20, the mobile device 1100 is configured to mate with the enclosing arrangement 1102. The enclosing arrangement 1102 contains a detection module 1200 integrated therewith. The detection module 1200 comprises a detection subsystem comprising an electrode input circuit similar to the detection subsystem 516 and electrode input circuit shown in FIG. 4 as electrode input/output interface circuit 401. Due to the similarity of the detection subsystem and electrode input circuit components, the particular details will not be repeated here for the sake of conciseness and clarity of disclosure. The enclosing arrangement 1102 also includes electrodes 1202A and 1202B (not shown in FIG. 20 and shown in FIG. 21) to couple the patient to the detection module 1200. The detection module 1200 may be electrically coupled to functional modules of the mobile device 1100 to detect and process the unique electrical signature generated by the ingestible event marker system 106 (e.g., IEM device). The detection module 1200 may be electrically coupled to the functional modules of the mobile device 1100 using any suitable techniques such as, for example, inductive coupling, wireless transmission, electrical connector, and the like. One example of a housing comprising a suitable connector to electrically couple the detection module 1200 to the functional modules of the mobile device 1100 is described in connection with FIG. 21.



FIG. 21 illustrates one aspect of a enclosing arrangement 1102 for receiving a mobile device where the enclosing arrangement 1102 comprises a detection circuit 1200 for detecting an electrical signal generated by an ingestible event marker integrated therewith and a connector 1300 for electrically coupling the detection circuit 1200 to the functional modules of the mobile device. In use, the mobile device (not shown) is slidably inserted over the enclosing arrangement 1102 and plugged into the connector 1300. The electrodes 1202A, 1202B are used tot couple the patient to the detection module 1200. The connector 1300 couples the detection module 1200 to the functional modules of the mobile device 1100 (FIG. 20) for communication purposes, among other purposes. In one aspect, the detection module 1200 integrated with the enclosing arrangement 1102 is a standalone module and includes all the necessary electronic modules to detect the unique electrical current signature generated by the IEM device.


Turning now back to FIG. 4, which is a block functional diagram of one aspect of an authentication subsystem 306 for detecting and/or generating personal electrical signals to authenticate the user and prove the identity of the subject 100 (FIG. 1). The authentication subsystem 306 comprises an electrode input/output interface circuit 401 to receive/transmit electrical signals from/to the electrodes 104a, 104b. The authentication subsystem 306 can be configured to operate in receive mode, broadcast mode, or combinations thereof. In receive mode, the input/output interface circuit 401 receives electrical signals from the electrodes 104a, 104b. In broadcast mode, the input/output interface circuit 401 transmits electrical signals to the electrodes 104a, 104b.


A transbody conductive communication module 402 and a physiological sensing module 404 are electrically coupled to the electrode input/output interface circuit 401. In one aspect, the transbody conductive communication module 402 is implemented as a first, e.g., high, frequency (HF) signal chain and the physiological sensing module 404 is implemented as a second, e.g., low, frequency (LF) signal chain. Also shown are CMOS temperature sensing module 406 (for detecting ambient temperature) and a 3-axis accelerometer 408. The authentication subsystem 306 also comprises a processing engine 418 (for example, a microcontroller and digital signal processor), a non-volatile memory 410 (for data storage), and a wireless communication module 412 to receive data from and/or transmit data to another device, for example in a data download/upload action, respectively. In various aspects, the communication module 412 may comprise one or more transmitters/receivers (“transceiver”) modules. As used herein, the term “transceiver” may be used in a very general sense to include a transmitter, a receiver, or a combination of both, without limitation. In one aspect, the transbody conductive communication module 402 is configured to communicate with an ingestible event marker system 106 (FIGS. 1, 5). In receive mode, the transbody conductive communication module 402 is configured to receive a transconduction current signal from the subject 100 (FIG. 1) via at least one of the electrodes 104a, 104b (FIG. 1). In broadcast mode, the transbody conductive communication module 402 is configured to transmit a transconduction current signal to the subject 100 via at least one of the electrodes 104a, 104b (FIG. 1). In one aspect, the transbody conductive communication module 402 is configured as a skin or design cover for a mobile device.


The sensors 414 typically contact the subject 100 (FIG. 1), e.g., are removably attachable to the torso. In various aspects, the sensors 414 may be removably or permanently attached to the authentication subsystem 306. For example, the sensors 414 may be removably connected to another device by snapping metal studs. The sensors 414 may comprise, for example, various devices capable of sensing or receiving the physiologic data. The types of sensors 414 include, for example, electrodes such as biocompatible electrodes. The sensors 414 may be configured, for example, as a pressure sensor, a motion sensor, an accelerometer, an electromyography (EMG) sensor, an event marker system, a biopotential sensor, an electrocardiogram sensor, a temperature sensor, a tactile event marker sensor, and an impedance sensor.


The feedback module 416 may be implemented with software, hardware, circuitry, various devices, and combinations thereof. The function of the feedback module 416 is to provide communication with the subject 100 (FIG. 1) in a discreet, tactful, circumspect manner as described above. In various aspects the feedback module 416 may be implemented to communicate with the subject 100 using techniques that employ visual, audio, vibratory/tactile, olfactory, and taste.



FIG. 5 illustrates one aspect of an ingestible event marker system 106 configured to generate a unique transconductance signal for confirming the identity of a person. In various aspects the ingestible event marker system 106 can be used in association with any medication product, as mentioned above, to determine the origin of the medication and to confirm that at least one of the right type and the right dosage of medication was delivered to the patient and in some aspects to determine when a patient takes the medication product. The scope of the present disclosure, however, is not limited by the environment and the medication product that may be used with the system 106. For example, the system 106 may be activated either in wireless mode, in galvanic mode by placing the system 106 within a capsule and then placing the capsule within a conducting fluid, or a combination thereof, or exposing the system 106 to air. Once placed in a conducting fluid, for example, the capsule would dissolve over a period of time and release the system 106 into the conducting fluid. Thus, in one aspect, the capsule would contain the system 106 and no product. Such a capsule may then be used in any environment where a conducting fluid is present and with any product. For example, the capsule may be dropped into a container filled with jet fuel, salt water, tomato sauce, motor oil, or any similar product. Additionally, the capsule containing the system 106 may be ingested at the same time that any pharmaceutical product is ingested in order to record the occurrence of the event, such as when the product was taken.


In the specific example of the system 106 combined with a medication or pharmaceutical product, as the product or pill is ingested, or exposed to air, the system 106 is activated in galvanic mode. The system 106 controls conductance to produce a unique current signature that is detected by the electrodes 104a, 104b (FIGS. 1-4), for example, thereby transmitting a unique transconduction signal that authenticates the user as the owner of the computer system (e.g., the mobile device 102). When activated in wireless mode, the system controls modulation of capacitive plates to produce a unique voltage signature associated with the system 106 that is detected.


In one aspect, the system 106 includes a framework 502. The framework 502 is a chassis for the system 106 and multiple components are attached to, deposited upon, or secured to the framework 502. In this aspect of the system 106, a digestible material 504 is physically associated with the framework 502. The material 504 may be chemically deposited on, evaporated onto, secured to, or built-up on the framework all of which may be referred to herein as “deposit” with respect to the framework 502. The material 504 is deposited on one side of the framework 502. The materials of interest that can be used as material 504 include, but are not limited to: Cu, CuCl, or CuI. The material 504 is deposited by physical vapor deposition, electrodeposition, or plasma deposition, among other protocols. The material 504 may be from about 0.05 to about 500 μm thick, such as from about 5 to about 100 μm thick. The shape is controlled by shadow mask deposition, or photolithography and etching. Additionally, even though only one region is shown for depositing the material, each system 106 may contain two or more electrically unique regions where the material 504 may be deposited, as desired.


At a different side, which is the opposite side as shown in FIG. 5, another digestible material 506 is deposited, such that the materials 504, 506 are dissimilar and insulated from each other. Although not shown, the different side selected may be the side next to the side selected for the material 504. The scope of the present disclosure is not limited by the side selected and the term “different side” can mean any of the multiple sides that are different from the first selected side. In various aspects, the dissimilar material may be located at different positions on a same side. Furthermore, although the shape of the system is shown as a square, the shape may be any geometrically suitable shape. The materials 504, 506 are selected such that they produce a voltage potential difference when the system 106 is in contact with conducting liquid, such as body fluids. The materials of interest for material 506 include, but are not limited to: Mg, Zn, or other electronegative metals. As indicated above with respect to the material 504, the material 506 may be chemically deposited on, evaporated onto, secured to, or built-up on the framework. Also, an adhesion layer may be necessary to help the material 506 (as well as material 504 when needed) to adhere to the framework 502. Typical adhesion layers for the material 506 are Ti, TiW, Cr or similar material. Anode material and the adhesion layer may be deposited by physical vapor deposition, electrodeposition or plasma deposition. The material 506 may be from about 0.05 to about 500 μm thick, such as from about 5 to about 100 μm thick. However, the scope of the present disclosure is not limited by the thickness of any of the materials nor by the type of process used to deposit or secure the materials to the framework 502.


According to the disclosure set forth, the materials 504, 506 can be any pair of materials with different electrochemical potentials. Additionally, in the aspects wherein the system 106 is used in-vivo, the materials 504, 506 may be vitamins that can be absorbed. More specifically, the materials 504, 506 can be made of any two materials appropriate for the environment in which the system 106 will be operating. For example, when used with an ingestible product, the materials 504, 506 are any pair of materials with different electrochemical potentials that are ingestible. An illustrative example includes the instance when the system 106 is in contact with an ionic solution, such as stomach acids, fluids excreted through the surface of the skin, fluids present below the surface of the skin, for example. Suitable materials are not restricted to metals, and in certain aspects the paired materials are chosen from metals and non-metals, e.g., a pair made up of a metal (such as Mg) and a salt (such as CuCl or CuI). With respect to the active electrode materials, any pairing of substances—metals, salts, or intercalation compounds—with suitably different electrochemical potentials (voltage) and low interfacial resistance are suitable.


Materials and pairings of interest include, but are not limited to, those reported in TABLE 1 below. In one aspect, one or both of the metals may be doped with a non-metal, e.g., to enhance the voltage potential created between the materials as they come into contact with a conducting liquid. Non-metals that may be used as doping agents in certain aspects include, but are not limited to: sulfur, iodine, and the like. In another aspect, the materials are copper iodine (CuI) as the anode and magnesium (Mg) as the cathode. Aspects of the present disclosure use electrode materials that are not harmful to the human body.











TABLE 1






Anode
Cathode







Metals
Magnesium,




Zinc Sodium




(†), Lithium




(†) Iron



Salts

Copper salts: iodide, chloride, bromide,




sulfate, formate, (other anions possible)




Fe3+ salts: e.g. orthophosphate,




pyrophosphate, (other anions possible)




Oxygen (††) on platinum, gold or




other catalytic surfaces


Intercalation
Graphite
Vanadium oxide Manganese oxide


compounds
with Li,




K, Ca, Na,




Mg









Thus, when the system 106 is in contact with the conducting fluid, a current path is formed through the conducting fluid between the dissimilar materials 504, 506. A control device 508 is secured to the framework 502 and electrically coupled to the materials 504, 506. The control device 508 includes electronic circuitry, for example control logic that is capable of controlling and altering the conductance between the materials 504, 506.


The voltage potential created between the dissimilar materials 504, 506 provides the power for operating the system as well as produces the current flow through the conducting fluid and the system 106. In one aspect, the system 106 operates in direct current mode. In an alternative aspect, the system 106 controls the direction of the current so that the direction of current is reversed in a cyclic manner, similar to alternating current. As the system reaches the conducting fluid or the electrolyte, where the fluid or electrolyte component is provided by a physiological fluid, e.g., stomach acid, the path for current flow between the dissimilar materials 504, 506 is completed external to the system 106; the current path through the system 106 is controlled by the control device 508. Completion of the current path allows for the current to flow and in turn a receiver, not shown, can detect the presence of the current and recognize that the system 106 has been activate and the desired event is occurring or has occurred.


In one aspect, the two dissimilar materials 504, 506 are similar in function to the two electrodes needed for a direct current power source, such as a battery. The conducting liquid acts as the electrolyte needed to complete the power source. The completed power source described is defined by the physical chemical reaction between the dissimilar materials 504, 506 of the system 106 and the surrounding fluids of the body. The completed power source may be viewed as a power source that exploits reverse electrolysis in an ionic or a conduction solution such as gastric fluid, blood, or other bodily fluids and some tissues. Additionally, the environment may be something other than a body and the liquid may be any conducting liquid. For example, the conducting fluid may be salt water or a metallic based paint.


In certain aspects, the two dissimilar materials 504, 506 are shielded from the surrounding environment by an additional layer of material. Accordingly, when the shield is dissolved and the two dissimilar materials 504, 506 are exposed to the target site, a voltage potential is generated.


In certain aspects, the complete power source or supply is one that is made up of active electrode materials, electrolytes, and inactive materials, such as current collectors, packaging. The active materials are any pair of materials with different electrochemical potentials. Suitable materials are not restricted to metals, and in certain aspects the paired materials are chosen from metals and non-metals, e.g., a pair made up of a metal (such as Mg) and a salt (such as CuI). With respect to the active electrode materials, any pairing of substances—metals, salts, or intercalation compounds—with suitably different electrochemical potentials (voltage) and low interfacial resistance are suitable.


A variety of different materials may be employed as the materials that form the electrodes. In certain aspects, electrode materials are chosen to provide for a voltage upon contact with the target physiological site, e.g., the stomach, sufficient to drive the system of the identifier. In certain aspects, the voltage provided by the electrode materials upon contact of the metals of the power source with the target physiological site is 0.001 V or higher, including 0.01 V or higher, such as 0.1 V or higher, e.g., 0.3 V or higher, including 0.5 volts or higher, and including 1.0 volts or higher, where in certain aspects, the voltage ranges from about 0.001 to about 10 volts, such as from about 0.01 to about 10 V.


Referring still to FIG. 5, the dissimilar materials 504, 506 provide the voltage potential to activate the control device 508. Once the control device 508 is activated or powered up, the control device 508 can alter conductance between the first and second materials 504, 506 in a unique manner. By altering the conductance between the first and second materials 504, 506, the control device 508 is capable of controlling the magnitude of the current through the conducting liquid that surrounds the system 106. This produces a unique current signature that can be detected and measured by a receiver (not shown), which can be positioned internal or external to the body. The receiver is disclosed in greater detail in U.S. patent application Ser. No. 12/673,326 entitled “BODY-ASSOCIATED RECEIVER AND METHOD” filed on Dec. 15, 2009, and published as 2010-0312188 A1 dated Dec. 9, 2010 which is incorporated herein by reference in its entirety. In addition to controlling the magnitude of the current path between the materials, non-conducting materials, membrane, or “skirt” are used to increase the “length” of the current path and, hence, act to boost the conductance path, as disclosed in the U.S. patent application Ser. No. 12/238,345 entitled, “IN-BODY DEVICE WITH VIRTUAL DIPOLE SIGNAL AMPLIFICATION” filed Sep. 25, 2008, the entire content of which is incorporated herein by reference. Alternatively, throughout the disclosure herein, the terms “non-conducting material,” “membrane,” and “skirt” are interchangeably used with the term “current path extender” without impacting the scope or the present aspects and the claims herein. The skirt, shown in portion at 505, 507, respectively, may be associated with, e.g., secured to, the framework 502. Various shapes and configurations for the skirt are contemplated as within the scope of the various aspects of the present invention. For example, the system 106 may be surrounded entirely or partially by the skirt and the skirt maybe positioned along a central axis of the system 106 or off-center relative to a central axis. Thus, the scope of the present invention as claimed herein is not limited by the shape or size of the skirt. Furthermore, in other aspects, the dissimilar materials 504, 506 may be separated by one skirt that is positioned in any defined region between the dissimilar materials 504, 506.


The system 106 may be grounded through a ground contact. The system 106 also may include a sensor module. In operation, ion or current paths are established between the first material 504 to the second material 506 and through a conducting fluid in contact with the system 106. The voltage potential created between the first and second materials 504, 506 is created through chemical reactions between the first and second materials 504, 506 and the conducting fluid. In one aspect, the surface of the first material 504 is not planar, but rather an irregular surface. The irregular surface increases the surface area of the material and, hence, the area that comes in contact with the conducting fluid.


In one aspect, at the surface of the first material 504, there is chemical reaction between the material 504 and the surrounding conducting fluid such that mass is released into the conducting fluid. The term mass as used herein refers to protons and neutrons that form a substance. One example includes the instant where the material is CuCl and when in contact with the conducting fluid, CuCl becomes Cu (solid) and Cl— in solution. The flow of ions into the conduction fluid is via ion paths. In a similar manner, there is a chemical reaction between the second material 506 and the surrounding conducting fluid and ions are captured by the second material 506. The release of ions at the first material 504 and capture of ion by the second material 506 is collectively referred to as the ionic exchange. The rate of ionic exchange and, hence the ionic emission rate or flow, is controlled by the control device 508. The control device 508 can increase or decrease the rate of ion flow by altering the conductance, which alters the impedance, between the first and second materials 504, 506. Through controlling the ion exchange, the system 106 can encode information in the ionic exchange process. Thus, the system 106 uses ionic emission to encode information in the ionic exchange.


The control device 508 can vary the duration of a fixed ionic exchange rate or current flow magnitude while keeping the rate or magnitude near constant, similar to when the frequency is modulated and the amplitude is constant. Also, the control device 508 can vary the level of the ionic exchange rate or the magnitude of the current flow while keeping the duration near constant. Thus, using various combinations of changes in duration and altering the rate or magnitude, the control device 508 encodes information in the current flow or the ionic exchange. For example, the control device 508 may use, but is not limited to any of the following techniques namely, Binary Phase-Shift Keying (PSK), Frequency Modulation (FM), Amplitude Modulation (AM), On-Off Keying, and PSK with On-Off Keying.


Various aspects of the system 106 may comprise electronic components as part of the control device 508. Components that may be present include but are not limited to: logic and/or memory elements, an integrated circuit, an inductor, a resistor, and sensors for measuring various parameters. Each component may be secured to the framework and/or to another component. The components on the surface of the support may be laid out in any convenient configuration. Where two or more components are present on the surface of the solid support, interconnects may be provided.


The system 106 controls the conductance between the dissimilar materials and, hence, the rate of ionic exchange or the current flow. Through altering the conductance in a specific manner the system is capable of encoding information in the ionic exchange and the current signature. The ionic exchange or the current signature is used to uniquely identify the specific system. Additionally, the system 106 is capable of producing various different unique exchanges or signatures and, thus, provides additional information. For example, a second current signature based on a second conductance alteration pattern may be used to provide additional information, which information may be related to the physical environment. To further illustrate, a first current signature may be a very low current state that maintains an oscillator on the chip and a second current signature may be a current state at least a factor of ten higher than the current state associated with the first current signature.


Having now described the basic elements of a personal authentication system, the disclosure now turns to a description of various aspects of authentication systems. FIG. 6 illustrates one aspect of an authentication system 600 comprising a target authentication device 602 and an authentication module comprising a body-associated device 112. The target authentication device 602 comprises an authentication receiver module 601. The body-associated device 112 comprises a transmission device 603. In one embodiment, the body-associated device 112 is destroyed when it is removed from the body of the subject 100.


The body-associated device 112 is located on the surface of the skin and is electrically coupled to the subject 100 via electrodes 604a, 604b. In one aspect, the body-associated device 112 comprises a transmission device 603 that is configured, or programmed, with a secret code 606 that is stored in memory 608, such as a password or a private key for more sophisticated authentication mechanisms. The body-associated device 112 acts in broadcast mode (opposite to the receive mode). The secret code 606 is read from the memory 608 and is encoded into a signal 610 by an encoder 612. The encoded signal 610 is converted to an electrically conductive signal 614 by the I/O interface circuit 616. The encoded electrically conductive signal 614 is applied to the body 617 of the subject 100 via the electrodes 604a, 604b. A battery Vbatt may be included in the body-associated device as a power source. Alternatively, a power source may be implemented by coupling energy through the electrodes 604a, 604b from the target authentication device 602. In yet another alternative, a power source similar to the power source described in connection with the ingestible event marker 106 (FIG. 5) may be employed where the power source may be activated by fluid excreted on the surface of the skin of the subject 100.


The electrically conductive signal 614 is conducted through the body 617 of the subject 100 to the authentication receiver module 601 of the target authentication device 602. Electrodes 618a, 618b detect the electrically conductive signal 614 from the body 617 and are coupled to a decoder 619 though an I/O interface circuit 620. The decoder 619 decodes the electrically conductive signal 614. The decoded code 622 is then compared by compare module 624 to established criteria 626. When the code 622 matches the established criteria 626, compare module 624 provides the results to the processor 628, which determines whether the electrical signal matches the predetermined criteria to authenticate the identity of the user based on the an electrical signal. If a match occurs, the processor 629 unlocks the target authentication device 602 and enables access by the subject 100. In one aspect, the authentication receiver module 601 is configured to encode the detected signal with a secret and retransmit the encoded signal back to the receiver module where it is compared to an expected result dependent on the mathematical properties of the encoding and the secret. In one aspect, the authentication receiver module 601 is configured to authenticate a challenge-response authentication, which is an authentication process that verifies an identity by requiring correct authentication information to be provided in response to a challenge. The authentication information may be usually a value that is computed in response to an unpredictable challenge value, but it may be just a password.


The target authentication device 602 may be any number of digital instruments. As previously discussed, the target authentication device 602 may be a mobile device 102 as described in connection with FIGS. 1-3. In other aspects, the target authentication device 602 may be any of the computer systems identified above. In one aspect, the target authentication device 602 may be located on a keyboard to ensure the identity of the user when the hands touch the keyboard, allowing the subject 100 to authenticate against web sites; a check-out terminal, which authenticates against the bank account of the subject 100 and allows the subject 100 to pay for transactions; a car that knows the subject 100 is the one holding the steering wheel and starts only for the subject 100; a doorknob that unlocks when authorized subjects 100 touch it; the target may even be another individual, so that when the subject 100 shake hands both parties are assured of the other's identity.


The body associated device 112 comprising the transmission device 603 may be a patch, implant, pendant, ring, article of clothing, piercing, or piece of jewelry. The body associated device 112 is physically and electrically associated with the subject 100, and contains a secret code 606.


In one aspect, the authentication receiver module 601 of the target authentication device 602 may comprise a transbody conductive communication module 402 as described in connection with FIG. 4, shown in phantom to indicate that it is optional. Communication could be over the same transconductive link established with the ingestible event marker system 106 described in FIG. 5, where the transmitter drives a dipole located on the body 617 of the subject 100 and the target authentication device 602 also contains a dipole for receiving the encoded signal. Alternatively, either the target authentication device 602 or the transmission device 603 or both may comprise a single electrode in contact with the body 617, with the counter electrode being a capacitive connection to free space. All of these cases ensure that both the transmission device 603 containing the authentication code 606 and the target authentication device 602 are both in conductive contact with the same body 617 in order for authentication to be successful.


In another aspect, the authentication receiver module 601 of the target authentication device 602 may comprise a physiological sensing module 404 as described in connection with FIG. 4, shown in phantom to indicate that it is optional. The physiological sensing module 404 may be employed to monitor biometric signatures associated with the subject 100 to establish that it is in fact attached to the subject 100. A profile of physiologic activity, based on parameters like heart rate, activity patterns, GSR, body temperature, circadian rhythms, and so forth may be generated on the body-associated device 112. This signature could be hashed with the authentication code 606 and transmitted to the target authentication device 602. The target authentication device 602 would then compare the biometric signature to a baseline database to confirm the subject 100. In one aspect, the biometric signature is derived from the at least one physiological signal and the biometric signature is compared to a user-associated signature. The user associated-signature may be derived from biometric data stored in a memory over time to generate a baseline biometric signature, wherein the authentication module device compares the biometric signature to the baseline biometric signature to authenticate the identity of the user. The user-associated biometric signature also may be derived from other sources outside this system.


In another aspect, the target authentication device 602 acquires a biometric profile over time and compares past readings against current ones. In this way, a sudden change could indicate that the body-associated device 112 has been removed from one person and put on another.


The secret authentication code 606 may be a simple password based authentication, in which case the password may be programmed into the transmission device 603, or the secret authentication code 606 may be a more complex challenge-response scheme where bidirectional communication is used to establish authentication over a public channel. Other established authentication schemes known in the art are also applicable to this case.


In yet another aspect, is to put a lock on the body-associated device 112 of some kind. A PIN code or tap pattern could be required to unlock the body-associated device 112 and enable it to broadcast the key transconductively (e.g., use the body 617 of the subject 100 as a conductive medium to conduct a current).


The above is a specific instantiation of a key (in this case the body-associated device 112) communicating with and unlocking a lock (in this case the target authentication device 602, such as a mobile device 102, for example) via transconductive communication. In various other aspects, this may be generalized to a number of keys (e.g., patch, watch, key fob in pocket, smart shoes, jewelry, clothing, etc.) communicating with any number of locks (e.g., phone, computer, door, car, cash register, ATM, vending machine). In certain instances it may be beneficial for the communication to be two-way. For instance, in the case of a body-associated device 112 and a mobile device 102, the body-associated device 112 initiates a session by periodically broadcasting the authentication code 606. The mobile device 102 receives the code 606, verifies its authenticity and unlocks the mobile device 102 display 204 (FIGS. 2, 3). The mobile phone 102 may then send an acknowledgement back to the body-associated device 112 via transconduction or a wireless link, and the body-associated device 112 might then decide to download stored physiological data to the mobile device 102. In another instance, the body-associated device 112 may be pre-programmed for a limited number of authentications; after each time a pairing is established between the body-associated device 112 and the mobile device 102, a counter may be incremented until it reaches a limit and the body-associated device 112 is de-authorized.


In another aspect, the relationship between the target identification device 602 and the transmission device 603 can be broadened beyond security and use-related permissions to include assurance of use-related benefits and transactions. For example, in a loyalty management program related to the transmission device 603 (which in addition to the items listed above could include consumer-related product packaging such as drink containers), assured use by a specific individual could be confirmed by the transmission device 603, thereby allowing the loyalty or other benefits to be granted.


In another aspect, instead of being a personally associated authentication token, the transmission device 603 could serve as a value token, like a gift card or event pass. In this case, a temporary transmission device 603 like an adhesive sticker is sold in a conventional transaction. The buyer applies the adhesive sticker to his or her body 617, and the value is transferred to a mobile device 102 (FIGS. 1-3) upon contact with the body 617 of the subject 100. In another example, a club might apply a door key patch to customers that cannot be removed without rendering it inoperative to control access for the duration of an event.


In another aspect, the authentication process may be bidirectional in that the target authentication device 602 (e.g., the mobile device 102) can send a code through the body 617 of the subject 100 to the body-associated device 112 (e.g., a patch). The body-associated device 112 authenticates and sends a signal back to the target authentication device 602 which would then unlock. In another aspect, an electrical current signal from the ingestible event indicator system 106 may be sourced by a small implantable device, e.g., dog tag sized, that sends a signal that is collected by the target authentication device 602 for authentication. The implantable device also may be configured with a physiological sensing module 404 to collect other physiological information.


With reference now to FIGS. 1-6, in yet another aspect, a mobile device 102 could be modified to receive the transconduction signals produced by the ingestible event marker system 106 when the owner simply touches the mobile device 102. The transconduction signal carries authentication information that identifies the subject 100 touching the mobile device 102 as the rightful owner. This eliminates the need to manually enter a PIN, while still assuring that the rightful owner is the subject 100 accessing the target authentication device 102.


In one aspect, the source of the transconduction signal could be an ingested ingestible event marker system 106 or other transconduction signal transmission source, such as a body-associated device 112 or similar transmission device 603 in direct contact with the body 617 of the subject 100. This includes transmitters implanted in the body 617 of the subject 100.



FIG. 7 illustrates one aspect of an authentication system 700 comprising a target authentication device 602 and an authentication transmission module comprising an implantable body-associated device 113 that is located below the skin of the subject 100. The implantable body-associated device 113 is similar in functionality to the body-associated device 112 described in connection with FIG. 6, with the exception that the implantable body-associated device 113 is shown in phantom to indicate that it is implanted below the skin of the subject 100.



FIG. 8 illustrates one aspect of an authentication system 800 comprising a target authentication device 602 and an authentication transmission module comprising and an event marker system 805. The target authentication device 602 comprises an authentication receiver module 601. The event marker system 805 is located on the on or under the skin of the subject 100 and generates transbody conductive signals representative of an authentication code. The event marker system 805 comprises a transmission device 803.


The event marker system 805 is located on the surface of the skin and is electrically coupled to the subject 100 via electrodes 604a, 604b. In one aspect, the event marker system 805 comprises a transmission device 803 that is configured, or programmed, with a secret code 806 that is stored in memory 808, such as a password or a private key for more sophisticated authentication mechanisms. The event marker system 805 acts in broadcast mode. The secret code 806 is read from the memory 808 and is encoded into a signal 810 by an encoder 812. The encoded signal 810 is converted to an electrically conductive signal 814 by the I/O interface circuit 816. The encoded electrically conductive signal 814 is applied to the body 617 of the subject 100 via the electrodes 604a, 604b.


In various aspects, the event marker system 805 may include a power source, such as a power source made up of a pair of electrodes fabricated from dissimilar materials. The event marker system 805 may generate electrical power when it comes into contact with fluids excreted by the skin. Otherwise, the event marker system 805 is functionally equivalent to the operation of the ingestible event marker 106 discussed in connection with FIG. 5. It will be appreciated, however, that in certain circumstances a small battery may be provided in the event marker system 805. The event marker system 805 also may include a second power source electrically coupled to the non-conductive communication module, such as a coil, e.g., an RFID coil.


The electrically conductive signal 814 is conducted through the body 617 of the subject 100 to the authentication receiver module 601 of the target authentication device 602. Electrodes 618a, 618b detect the electrically conductive signal 814 from the body 617 and are coupled to a decoder 619 though an I/O interface circuit 620. The decoder 619 decodes the electrically conductive signal 814. The decoded code 622 is then compared by compare module 624 to established criteria 626. When the code 622 matches the established criteria 626, compare module 624 signals the processor 628, which determines whether the electrical signal matches the predetermined criteria to authenticate the identity of the user based on the an electrical signal. If a match occurs, the processor 629 unlocks the target authentication device 602 and enables access by the subject 100.


In some embodiments of interest, a non-conductive communication module may be provided, which is a wireless radio-frequency module. While the wireless radio-frequency communication module may vary, in some instances this module is a radio-frequency identification (RFID) module. For ease of description purposes only, embodiments of the invention will now be further described in terms of embodiments where the non-conductive communication module is an RFID communication module. However, as noted above the non-conductive communication module may vary widely.


In some instances, the RFID module incorporates, for example, an integrated circuit and an RF antenna. The RFID module may be communicatively associated with a conductive module incorporating, for example, an integrated circuit and a conductive antenna. Either of the RFID module or the conductive module, or both, may function in conjunction with medication and/or medication packaging to receive, process, store, and/or transmit information related to or associated with the medication. As indicated above, the devices and systems can be used across multiple and varied applications to provide secure, controlled, and accurate communications in viable, cost-effective implementations.


Although the present disclosure has been described in connection with a mobile phone, the application may be broadly extended to include other instances where a person needs to authenticate to a system, including, for example access through a locked door, access through a turnstile to get on the subway or into an entertainment venue, access to a computer, access to an ATM or payment terminal at a retailer, access to any other target authentication device 602 described herein.


In one aspect, the authentication receiver module is located inside of an extension chamber on the back of a mobile phone 102 housing 202 (FIG. 2). The electrode connections on the module are wired directly to two electrodes 618a, 618b in the form of metal buttons exposed on the back of the mobile phone housing 202. When the user touches the electrodes 618a, 618b with fingers from the left and right hand, the transbody conductive communication module 402 detects transconduction signals from an ingestible event marker system 106 or from a similar signal generated by an electronic pill emulator. In one aspect, the transbody conductive communication module 402 communicates to the target authentication device 602 via a short range wireless connection, such as Bluetooth, for example. A software module running on the target authentication device 602 monitors detection data delivered from the transbody conductive communication module 402 and flips its display from Locked to Authorized to show that the transconduction signal has been received. In an authentication system, the payload sent in the transconduction signal is configured to be secure and personal to the owner. The receiver is hard-wired directly into the electronics of the target authentication device 602, eliminating the Bluetooth link between receiver and phone.


With reference to FIG. 9, there is shown one aspect of an ingestible device event indicator system with dissimilar metals positioned on opposite ends as system 2030. The system 2030 can be used in association with any pharmaceutical product, as mentioned above, to determine when a patient takes the pharmaceutical product. As indicated above, the scope of the present invention is not limited by the environment and the product that is used with the system 2030. For example, the system 2030 may be placed within a capsule and the capsule is placed within the conducting liquid. The capsule would then dissolve over a period of time and release the system 2030 into the conducting liquid. Thus, in one aspect, the capsule would contain the system 2030 and no product. Such a capsule may then be used in any environment where a conducting liquid is present and with any product. For example, the capsule may be dropped into a container filled with jet fuel, salt water, tomato sauce, motor oil, or any similar product. Additionally, the capsule containing the system 2030 may be ingested at the same time that any pharmaceutical product is ingested in order to record the occurrence of the event, such as when the product was taken.


In the specific example of the system 2030 combined with the pharmaceutical product, as the product or pill is ingested, the system 2030 is activated. The system 2030 controls conductance to produce a unique current signature that is detected, thereby signifying that the pharmaceutical product has been taken. The system 2030 includes a framework 2032. The framework 2032 is a chassis for the system 2030 and multiple components are attached to, deposited upon, or secured to the framework 2032. In this aspect of the system 2030, a digestible material 2034 is physically associated with the framework 2032. The material 2034 may be chemically deposited on, evaporated onto, secured to, or built-up on the framework all of which may be referred to herein as “deposit” with respect to the framework 2032. The material 2034 is deposited on one side of the framework 2032. The materials of interest that can be used as material 2034 include, but are not limited to: Cu or CuI. The material 2034 is deposited by physical vapor deposition, electrodeposition, or plasma deposition, among other protocols. The material 2034 may be from about 0.05 to about 500 .mu.m thick, such as from about 5 to about 100 .mu.m thick. The shape is controlled by shadow mask deposition, or photolithography and etching. Additionally, even though only one region is shown for depositing the material, each system 2030 may contain two or more electrically unique regions where the material 2034 may be deposited, as desired.


At a different side, which is the opposite side as shown in FIG. 9, another digestible material 2036 is deposited, such that materials 2034 and 2036 are dissimilar. Although not shown, the different side selected may be the side next to the side selected for the material 2034. The scope of the present invention is not limited by the side selected and the term “different side” can mean any of the multiple sides that are different from the first selected side. Furthermore, even though the shape of the system is shown as a square, the shape maybe any geometrically suitable shape. Material 2034 and 2036 are selected such that they produce a voltage potential difference when the system 2030 is in contact with conducting liquid, such as body fluids. The materials of interest for material 2036 include, but are not limited to: Mg, Zn, or other electronegative metals. As indicated above with respect to the material 2034, the material 2036 may be chemically deposited on, evaporated onto, secured to, or built-up on the framework. Also, an adhesion layer may be necessary to help the material 2036 (as well as material 2034 when needed) to adhere to the framework 2032. Typical adhesion layers for the material 2036 are Ti, TiW, Cr or similar material. Anode material and the adhesion layer may be deposited by physical vapor deposition, electrodeposition or plasma deposition. The material 2036 may be from about 0.05 to about 500 .mu.m thick, such as from about 5 to about 100 .mu.m thick. However, the scope of the present invention is not limited by the thickness of any of the materials nor by the type of process used to deposit or secure the materials to the framework 2032.


Thus, when the system 2030 is in contact with the conducting liquid, a current path, an example is shown in FIG. 11, is formed through the conducting liquid between material 2034 and 2036. A control device 2038 is secured to the framework 2032 and electrically coupled to the materials 2034 and 2036. The control device 2038 includes electronic circuitry, for example control logic that is capable of controlling and altering the conductance between the materials 2034 and 2036.


The voltage potential created between the materials 2034 and 2036 provides the power for operating the system as well as produces the current flow through the conducting fluid and the system. In one aspect, the system operates in direct current mode. In an alternative aspect, the system controls the direction of the current so that the direction of current is reversed in a cyclic manner, similar to alternating current. As the system reaches the conducting fluid or the electrolyte, where the fluid or electrolyte component is provided by a physiological fluid, e.g., stomach acid, the path for current flow between the materials 2034 and 2036 is completed external to the system 2030; the current path through the system 2030 is controlled by the control device 2038. Completion of the current path allows for the current to flow and in turn a receiver, not shown, can detect the presence of the current and recognize that the system 2030 has been activate and the desired event is occurring or has occurred.


In one aspect, the two materials 2034 and 2036 are similar in function to the two electrodes needed for a direct current power source, such as a battery. The conducting liquid acts as the electrolyte needed to complete the power source. The completed power source described is defined by the physical chemical reaction between the materials 2034 and 2036 of the system 2030 and the surrounding fluids of the body. The completed power source may be viewed as a power source that exploits reverse electrolysis in an ionic or a conductive solution such as gastric fluid, blood, or other bodily fluids and some tissues. Additionally, the environment may be something other than a body and the liquid may be any conducting liquid. For example, the conducting fluid may be salt water or a metallic based paint.


In certain aspects, these two materials are shielded from the surrounding environment by an additional layer of material. Accordingly, when the shield is dissolved and the two dissimilar materials are exposed to the target site, a voltage potential is generated.


Referring again to FIG. 9, the materials 2034 and 2036 provide the voltage potential to activate the control device 2038. Once the control device 2038 is activated or powered up, the control device 2038 can alter conductance between the materials 2034 and 2036 in a unique manner. By altering the conductance between materials 2034 and 2036, the control device 2038 is capable of controlling the magnitude of the current through the conducting liquid that surrounds the system 2030. This produces a unique current signature that can be detected and measured by a receiver (not shown), which can be positioned internal or external to the body. In addition to controlling the magnitude of the current path between the materials, non-conducting materials, membrane, or “skirt” are used to increase the “length” of the current path and, hence, act to boost the conductance path, as disclosed in the U.S. patent application Ser. No. 12/238,345 entitled, “In-Body Device with Virtual Dipole Signal Amplification” filed Sep. 25, 2008, the entire content of which is incorporated herein by reference. Alternatively, throughout the disclosure herein, the terms “non-conducting material”, “membrane”, and “skirt” are interchangeably with the term “current path extender” without impacting the scope or the present aspects and the claims herein. The skirt, shown in portion at 2035 and 2037, respectively, may be associated with, e.g., secured to, the framework 2032. Various shapes and configurations for the skirt are contemplated as within the scope of the present invention. For example, the system 2030 may be surrounded entirely or partially by the skirt and the skirt maybe positioned along a central axis of the system 2030 or off-center relative to a central axis. Thus, the scope of the present invention as claimed herein is not limited by the shape or size of the skirt. Furthermore, in other aspects, the materials 2034 and 2036 may be separated by one skirt that is positioned in any defined region between the materials 2034 and 2036.


Referring now to FIG. 10, in another aspect of an ingestible device is shown in more detail as system 2040. The system 2040 includes a framework 2042. The framework 2042 is similar to the framework 2032 of FIG. 9. In this aspect of the system 2040, a digestible or dissolvable material 2044 is deposited on a portion of one side of the framework 2042. At a different portion of the same side of the framework 2042, another digestible material 2046 is deposited, such that materials 2044 and 2046 are dissimilar. More specifically, material 2044 and 2046 are selected such that they form a voltage potential difference when in contact with a conducting liquid, such as body fluids. Thus, when the system 2040 is in contact with and/or partially in contact with the conducting liquid, then a current path, an example is shown in FIG. 11, is formed through the conducting liquid between material 2044 and 2046. A control device 2048 is secured to the framework 2042 and electrically coupled to the materials 2044 and 2046. The control device 2048 includes electronic circuitry that is capable of controlling part of the conductance path between the materials 2044 and 2046. The materials 2044 and 2046 are separated by a non-conducting skirt 2049. Various examples of the skirt 2049 are disclosed in U.S. Provisional Application No. 61/173,511 filed on Apr. 28, 2009 and entitled “HIGHLY RELIABLE INGESTIBLE EVENT MARKERS AND METHODS OF USING SAME” and U.S. Provisional Application No. 61/173,564 filed on Apr. 28, 2009 and entitled “INGESTIBLE EVENT MARKERS HAVING SIGNAL AMPLIFIERS THAT COMPRISE AN ACTIVE AGENT”; as well as U.S. application Ser. No. 12/238,345 filed Sep. 25, 2008 and published as 2009-0082645, entitled “IN-BODY DEVICE WITH VIRTUAL DIPOLE SIGNAL AMPLIFICATION”; the entire disclosure of each is incorporated herein by reference.


Once the control device 2048 is activated or powered up, the control device 2048 can alter conductance between the materials 2044 and 2046. Thus, the control device 2048 is capable of controlling the magnitude of the current through the conducting liquid that surrounds the system 2040. As indicated above with respect to system 2030, a unique current signature that is associated with the system 2040 can be detected by a receiver (not shown) to mark the activation of the system 2040. In order to increase the “length” of the current path the size of the skirt 2049 is altered. The longer the current path, the easier it may be for the receiver to detect the current.


Referring now to FIG. 11, the system 2030 of FIG. 9 is shown in an activated state and in contact with conducting liquid. The system 2030 is grounded through ground contact 2052. The system 2030 also includes a sensor module 2074, which is described in greater detail with respect to FIG. 11 Ion or current paths 2050 form between material 2034 to material 2036 through the conducting fluid in contact with the system 2030. The voltage potential created between the material 2034 and 2036 is created through chemical reactions between materials 2034/2036 and the conducting fluid.



FIG. 11A shows an exploded view of the surface of the material 2034. The surface of the material 2034 is not planar, but rather an irregular surface 2054 as shown. The irregular surface 2054 increases the surface area of the material and, hence, the area that comes in contact with the conducting fluid.


In one aspect, at the surface of the material 2034, there is chemical reaction between the material 2034 and the surrounding conducting fluid such that mass is released into the conducting fluid. The term “mass” as used herein refers to protons and neutrons that form a substance. One example includes the instant where the material is CuCl and when in contact with the conducting fluid, CuCl becomes Cu (solid) and Cl.sup.− in solution. The flow of ions into the conduction fluid is depicted by the ion paths 2050. In a similar manner, there is a chemical reaction between the material 2036 and the surrounding conducting fluid and ions are captured by the material 2036. The release of ions at the material 2034 and capture of ion by the material 2036 is collectively referred to as the ionic exchange. The rate of ionic exchange and, hence the ionic emission rate or flow, is controlled by the control device 2038. The control device 2038 can increase or decrease the rate of ion flow by altering the conductance, which alters the impedance, between the materials 2034 and 2036. Through controlling the ion exchange, the system 2030 can encode information in the ionic exchange process. Thus, the system 2030 uses ionic emission to encode information in the ionic exchange.


The control device 2038 can vary the duration of a fixed ionic exchange rate or current flow magnitude while keeping the rate or magnitude near constant, similar to when the frequency is modulated and the amplitude is constant. Also, the control device 2038 can vary the level of the ionic exchange rate or the magnitude of the current flow while keeping the duration near constant. Thus, using various combinations of changes in duration and altering the rate or magnitude, the control device 2038 encodes information in the current flow or the ionic exchange. For example, the control device 2038 may use, but is not limited to any of the following techniques namely, Binary Phase-Shift Keying (PSK), Frequency modulation, Amplitude modulation, on-off keying, and PSK with on-off keying.


As indicated above, the various aspects disclosed herein, such as systems 2030 and 2040 of FIGS. 9 and 10, respectively, include electronic components as part of the control device 2038 or the control device 2048. Components that may be present include but are not limited to: logic and/or memory elements, an integrated circuit, an inductor, a resistor, and sensors for measuring various parameters. Each component may be secured to the framework and/or to another component. The components on the surface of the support may be laid out in any convenient configuration. Where two or more components are present on the surface of the solid support, interconnects may be provided.


As indicated above, the system, such as system 2030 and 2040, control the conductance between the dissimilar materials and, hence, the rate of ionic exchange or the current flow. Through altering the conductance in a specific manner the system is capable of encoding information in the ionic exchange and the current signature. The ionic exchange or the current signature is used to uniquely identify the specific system. Additionally, the systems 2030 and 2040 are capable of producing various different unique exchanges or signatures and, thus, provide additional information. For example, a second current signature based on a second conductance alteration pattern may be used to provide additional information, which information may be related to the physical environment. To further illustrate, a first current signature may be a very low current state that maintains an oscillator on the chip and a second current signature may be a current state at least a factor of ten higher than the current state associated with the first current signature.


Referring now to FIG. 12, a block diagram representation of the control device 2038 is shown. The device 2030 includes a control module 2062, a counter or clock 2064, and a memory 2066. Additionally, the device 2038 is shown to include a sensor module 2072 as well as the sensor module 2074, which was referenced in FIG. 11. The control module 2062 has an input 2068 electrically coupled to the material 2034 and an output 2070 electrically coupled to the material 2036. The control module 2062, the clock 2064, the memory 2066, and the sensor modules 2072/2074 also have power inputs (some not shown). The power for each of these components is supplied by the voltage potential produced by the chemical reaction between materials 2034 and 2036 and the conducting fluid, when the system 2030 is in contact with the conducting fluid. The control module 2062 controls the conductance through logic that alters the overall impedance of the system 2030. The control module 2062 is electrically coupled to the clock 2064. The clock 2064 provides a clock cycle to the control module 2062. Based upon the programmed characteristics of the control module 2062, when a set number of clock cycles have passed, the control module 2062 alters the conductance characteristics between materials 2034 and 2036. This cycle is repeated and thereby the control device 2038 produces a unique current signature characteristic. The control module 2062 is also electrically coupled to the memory 2066. Both the clock 2064 and the memory 2066 are powered by the voltage potential created between the materials 2034 and 2036.


The control module 2062 is also electrically coupled to and in communication with the sensor modules 2072 and 2074. In the aspect shown, the sensor module 2072 is part of the control device 2038 and the sensor module 2074 is a separate component. In alternative aspects, either one of the sensor modules 2072 and 2074 can be used without the other and the scope of the present invention is not limited by the structural or functional location of the sensor modules 2072 or 2074. Additionally, any component of the system 2030 may be functionally or structurally moved, combined, or repositioned without limiting the scope of the present invention as claimed. Thus, it is possible to have one single structure, for example a processor, which is designed to perform the functions of all of the following modules: the control module 2062, the clock 2064, the memory 2066, and the sensor module 2072 or 2074. On the other hand, it is also within the scope of the present invention to have each of these functional components located in independent structures that are linked electrically and able to communicate.


Referring again to FIG. 12, the sensor modules 2072 or 2074 can include any of the following sensors: temperature, pressure, pH level, and conductivity. In one aspect, the sensor modules 2072 or 2074 gather information from the environment and communicate the analog information to the control module 2062. The control module then converts the analog information to digital information and the digital information is encoded in the current flow or the rate of the transfer of mass that produces the ionic flow. In another aspect, the sensor modules 2072 or 2074 gather information from the environment and convert the analog information to digital information and then communicate the digital information to control module 2062. In the aspect shown in FIG. 11, the sensor modules 2074 is shown as being electrically coupled to the material 2034 and 2036 as well as the control device 2038. In another aspect, as shown in FIG. 12, the sensor module 2074 is electrically coupled to the control device 2038 at connection 2078. The connection 2078 acts as both a source for power supply to the sensor module 2074 and a communication channel between the sensor module 2074 and the control device 2038.


Referring now to FIG. 11B, the system 2030 includes a pH sensor module 2076 connected to a material 2039, which is selected in accordance with the specific type of sensing function being performed. The pH sensor module 2076 is also connected to the control device 2038. The material 2039 is electrically isolated from the material 2034 by a non-conductive barrier 2055. In one aspect, the material 2039 is platinum. In operation, the pH sensor module 2076 uses the voltage potential difference between the materials 2034/2036. The pH sensor module 2076 measures the voltage potential difference between the material 2034 and the material 2039 and records that value for later comparison. The pH sensor module 2076 also measures the voltage potential difference between the material 2039 and the material 2036 and records that value for later comparison. The pH sensor module 2076 calculates the pH level of the surrounding environment using the voltage potential values. The pH sensor module 2076 provides that information to the control device 2038. The control device 2038 varies the rate of the transfer of mass that produces the ionic transfer and the current flow to encode the information relevant to the pH level in the ionic transfer, which can be detected by a receiver (not shown). Thus, the system 2030 can determine and provide the information related to the pH level to a source external to the environment.


As indicated above, the control device 2038 can be programmed in advance to output a pre-defined current signature. In another aspect, the system can include a receiver system that can receive programming information when the system is activated. In another aspect, not shown, the switch 2064 and the memory 2066 can be combined into one device.


In addition to the above components, the system 2030 may also include one or other electronic components. Electrical components of interest include, but are not limited to: additional logic and/or memory elements, e.g., in the form of an integrated circuit; a power regulation device, e.g., battery, fuel cell or capacitor; a sensor, a stimulator, etc.; a signal transmission element, e.g., in the form of an antenna, electrode, coil, etc.; a passive element, e.g., an inductor, resistor, etc.



FIG. 13 provides a functional block diagram of how a receiver may implement a coherent demodulation protocol, according to one aspect of the invention. It should be noted that only a portion of the receiver is shown in FIG. 13. FIG. 13 illustrates the process of mixing the signal down to baseband once the carrier frequency (and carrier signal mixed down to carrier offset) is determined. A carrier signal 2221 is mixed with a second carrier signal 2222 at mixer 2223. A narrow low-pass filter 2220 is applied of appropriate bandwidth to reduce the effect of out-of-bound noise. Demodulation occurs at functional blocks 2225 in accordance with the coherent demodulation scheme of the present invention. The unwrapped phase 2230 of the complex signal is determined. An optional third mixer stage, in which the phase evolution is used to estimate the frequency differential between the calculated and real carrier frequency can be applied. The structure of the packet is then leveraged to determine the beginning of the coding region of the BPSK signal at block 2240. Mainly, the presence of the sync header, which appears as an FM porch in the amplitude signal of the complex demodulated signal is used to determine the starting bounds of the packet. Once the starting point of the packet is determined the signal is rotated at block 2250 on the IQ plane and standard bit identification and eventually decoded at block 2260.


In addition to demodulation, the transbody communication module may include a forward error correction module, which module provides additional gain to combat interference from other unwanted signals and noise. Forward error correction functional modules of interest include those described in PCT Application Serial No. PCT/US2007/024225; the disclosure of which is herein incorporated by reference. In some instances, the forward error correction module may employ any convenient protocol, such as Reed-Solomon, Golay, Hamming, BCH, and Turbo protocols to identify and correct (within bounds) decoding errors.


Receivers of the invention may further employ a beacon functionality module. In various aspects, the beacon switching module may employ one or more of the following: a beacon wakeup module, a beacon signal module, a wave/frequency module, a multiple frequency module, and a modulated signal module.


The beacon switching module may be associated with beacon communications, e.g., a beacon communication channel, a beacon protocol, etc. For the purpose of the present disclosure, beacons are typically signals sent either as part of a message or to augment a message (sometimes referred to herein as “beacon signals”). The beacons may have well-defined characteristics, such as frequency. Beacons may be detected readily in noisy environments and may be used for a trigger to a sniff circuit, such as described below. In one aspect, the beacon switching module may comprise the beacon wakeup module, having wakeup functionality. Wakeup functionality generally comprises the functionality to operate in high power modes only during specific times, e.g., short periods for specific purposes, to receive a signal, etc. An important consideration on a receiver portion of a system is that it be of low power. This feature may be advantageous in an implanted receiver, to provide for both small size and to preserve a long-functioning electrical supply from a battery. The beacon switching module enables these advantages by having the receiver operate in a high power mode for very limited periods of time. Short duty cycles of this kind can provide optimal system size and energy draw features.


In practice, the receiver may “wake up” periodically, and at low energy consumption, to perform a “sniff function” via, for example, a sniff circuit. For the purpose of the present application, the term “sniff function” generally refers to a short, low-power function to determine if a transmitter is present. If a transmitter signal is detected by the sniff function, the device may transition to a higher power communication decode mode. If a transmitter signal is not present, the receiver may return, e.g., immediately return, to sleep mode. In this manner, energy is conserved during relatively long periods when a transmitter signal is not present, while high-power capabilities remain available for efficient decode mode operations during the relatively few periods when a transmit signal is present. Several modes, and combination thereof, may be available for operating the sniff circuit. By matching the needs of a particular system to the sniff circuit configuration, an optimized system may be achieved.


Another view of a beacon module is provided in the functional block diagram shown in FIG. 14. The scheme outlined in FIG. 14 outlines one technique for identifying a valid beacon. The incoming signal 2360 represents the signals received by electrodes, bandpass filtered (such as from 10 KHz to 34 KHz) by a high frequency signaling chain (which encompasses the carrier frequency), and converted from analog to digital. The signal 2360 is then decimated at block 2361 and mixed at the nominal drive frequency (such as, 12.5 KHz, 20 KHz, etc.) at mixer 2362. The resulting signal is decimated at block 2364 and low-pass filtered (such as 5 KHz BW) at block 2365 to produce the carrier signal mixed down to carrier offset—signal 2369. Signal 2369 is further processed by blocks 2367 (fast Fourier transform and then detection of two strongest peaks) to provide the true carrier frequency signal 2368. This protocol allows for accurate determination of the carrier frequency of the transmitted beacon.



FIG. 15 provides a block functional diagram of an integrated circuit component of a signal receiver according to an aspect of the invention. In FIG. 15, receiver 2700 includes electrode input 2710. Electrically coupled to the electrode input 2710 are transbody conductive communication module 2720 and physiological sensing module 2730. In one aspect, transbody conductive communication module 2720 is implemented as a high frequency (HF) signal chain and physiological sensing module 2730 is implemented as a low frequency (LF) signal chain. Also shown are CMOS temperature sensing module 2740 (for detecting ambient temperature) and a 3-axis accelerometer 2750. Receiver 2700 also includes a processing engine 2760 (for example, a microcontroller and digital signal processor), non-volatile memory 2770 (for data storage) and wireless communication module 2780 (for data transmission to another device, for example in a data upload action).



FIG. 16 provides a more detailed block diagram of a circuit configured to implement the block functional diagram of the receiver depicted in FIG. 15, according to one aspect of the invention. In FIG. 16, receiver 800 includes electrodes e1, e2 and e3 (2811, 2812 and 2813) which, for example, receive the conductively transmitted signals by an IEM and/or sense physiological parameters or biomarkers of interest. The signals received by the electrodes 2811, 2812, and 2813 are multiplexed by multiplexer 820 which is electrically coupled to the electrodes.


Multiplexer 2820 is electrically coupled to both high band pass filter 2830 and low band pass filter 2840. The high and low frequency signal chains provide for programmable gain to cover the desired level or range. In this specific aspect, high band pass filter 2830 passes frequencies in the 10 KHz to 34 KHz band while filtering out noise from out-of-band frequencies. This high frequency band may vary, and may include, for example, a range of 3 KHz to 300 KHz. The passing frequencies are then amplified by amplifier 2832 before being converted into a digital signal by converter 2834 for input into high power processor 2880 (shown as a DSP) which is electrically coupled to the high frequency signal chain.


Low band pass filter 2840 is shown passing lower frequencies in the range of 0.5 Hz to 150 Hz while filtering out out-of-band frequencies. The frequency band may vary, and may include, for example, frequencies less than 300 Hz, such as less than 200 Hz, including less than 150 Hz. The passing frequency signals are amplified by amplifier 842. Also shown is accelerometer 850 electrically coupled to second multiplexer 2860. Multiplexer 2860 multiplexes the signals from the accelerometer with the amplified signals from amplifier 2842. The multiplexed signals are then converted to digital signals by converter 864 which is also electrically coupled to low power processor 2870.


In one aspect, a digital accelerometer (such as one manufactured by Analog Devices), may be implemented in place of accelerometer 2850. Various advantages may be achieved by using a digital accelerometer. For example, because the signals the digital accelerometer would produce signals already in digital format, the digital accelerometer could bypass converter 2864 and electrically couple to the low power microcontroller 2870—in which case multiplexer 2860 would no longer be required. Also, the digital signal may be configured to turn itself on when detecting motion, further conserving power. In addition, continuous step counting may be implemented. The digital accelerometer may include a FIFO buffer to help control the flow of data sent to the low power processor 2870. For instance, data may be buffered in the FIFO until full, at which time the processor may be triggered to turn awaken from an idle state and receive the data.


Low power processor 2870 may be, for example, an MSP430 microcontroller from Texas Instruments. Low power processor 2870 of receiver 2800 maintains the idle state, which as stated earlier, requires minimal current draw—e.g., 10 μA or less, or 1 μA or less.


High power processor 2880 may be, for example, a VC5509 digital signal process from Texas Instruments. The high power processor 2880 performs the signal processing actions during the active state. These actions, as stated earlier, require larger amounts of current than the idle state—e.g., currents of 30 μA or more, such as 50 μA or more—and may include, for example, actions such as scanning for conductively transmitted signals, processing conductively transmitted signals when received, obtaining and/or processing physiological data, etc.


The receiver may include a hardware accelerator module to process data signals. The hardware accelerator module may be implemented instead of, for example, a DSP. Being a more specialized computation unit, it performs aspects of the signal processing algorithm with fewer transistors (less cost and power) compared to the more general purpose DSP. The blocks of hardware may be used to “accelerate” the performance of important specific function(s). Some architectures for hardware accelerators may be “programmable” via microcode or VLIW assembly. In the course of use, their functions may be accessed by calls to function libraries.


The hardware accelerator (HWA) module comprises an HWA input block to receive an input signal that is to be processed and instructions for processing the input signal; and, an HWA processing block to process the input signal according to the received instructions and to generate a resulting output signal. The resulting output signal may be transmitted as needed by an HWA output block.


Also shown in FIG. 16 is flash memory 2890 electrically coupled to high power processor 2880. In one aspect, flash memory 2890 may be electrically coupled to low power processor 2870, which may provide for better power efficiency.


Wireless communication element 2895 is shown electrically coupled to high power processor 2880 and may include, for example, a BLUETOOTH™ wireless communication transceiver. In one aspect, wireless communication element 2895 is electrically coupled to high power processor 2880. In another aspect, wireless communication element 2895 is electrically coupled to high power processor 2880 and low power processor 2870. Furthermore, wireless communication element 2895 may be implemented to have its own power supply so that it may be turned on and off independently from other components of the receiver—e.g., by a microprocessor.



FIG. 17 provides a view of a block diagram of hardware in a receiver according to an aspect of the invention related to the high frequency signal chain. In FIG. 17, receiver 2900 includes receiver probes (for example in the form of electrodes 2911, 2912 and 2913) electrically coupled to multiplexer 2920. Also shown are high pass filter 2930 and low pass filter 2940 to provide for a band pass filter which eliminates any out-of-band frequencies. In the aspect shown, a band pass of 10 KHz to 34 KHz is provided to pass carrier signals falling within the frequency band. Example carrier frequencies may include, but are not limited to, 12.5 KHz and 20 KHz. One or more carriers may be present. In addition, receiver 2900 includes analog to digital converter 2950—for example, sampling at 500 KHz. The digital signal can thereafter be processed by the DSP. Shown in this aspect is DMA to DSP unit 960 which sends the digital signal to dedicated memory for the DSP. The direct memory access provides the benefit of allowing the rest of the DSP to remain in a low power mode.


Example Configurations for Various States

As stated earlier, for each receiver state, the high power functional block may be cycled between active and inactive states accordingly. Also, for each receiver state, various receiver elements (such as circuit blocks, power domains within processor, etc.) of a receiver may be configured to independently cycle from on and off by the power supply module. Therefore, the receiver may have different configurations for each state to achieve power efficiency.


In certain aspects, the receivers are part of a body-associated system or network of devices, such as sensors, signal receivers, and optionally other devices, which may be internal and/or external, which provide a variety of different types of information that is ultimately collected and processed by a processor, such as an external processor, which then can provide contextual data about a living subject, such as a patient, as output. For example, the receiver may be a member of an in-body network of devices which can provide an output that includes data about IEM ingestion, one or more physiological sensed parameters, implantable device operation, etc., to an external collector of the data. The external collector, e.g., in the form of a health care network server, etc., of the data then combines this receiver provided data with additional relevant data about the patient, e.g., weight, weather, medical record data, etc., and may process this disparate data to provide highly specific and contextual patient specific data.


Systems of the invention include, in certain aspects, a signal receiver aspect of a receiver and one or more IEMs. IEMs of interest include those described in PCT application serial no. PCT/US2006/016370 published as WO/2006/116718; PCT application serial no. PCT/US2007/082563 published as WO/2008/052136; PCT application serial no. PCT/US2007/024225 published as WO/2008/063626; PCT application serial no. PCT/US2007/022257 published as WO/2008/066617; PCT application serial no. PCT/US2008/052845 published as WO/2008/095183; PCT application serial no. PCT/US2008/053999 published as WO/2008/101107; PCT application serial no. PCT/US2008/056296 published as WO/2008/112577; PCT application serial no. PCT/US2008/056299 published as WO/2008/112578; and PCT application serial no. PCT/US2008/077753 published as WO 2009/042812; the disclosures of which applications are herein incorporated by reference.


In certain aspects the systems include an external device which is distinct from the receiver (which may be implanted or topically applied in certain aspects), where this external device provides a number of functionalities. Such an external device can include the capacity to provide feedback and appropriate clinical regulation to the patient. Such a device can take any of a number of forms. For example, the device can be configured to sit on the bed next to the patient, e.g., a bedside monitor. Other formats include, but are not limited to, PDAs, smart phones, home computers, etc.


An example of a system of the invention is shown in FIG. 18A. In FIG. 18A, system 1500 includes a pharmaceutical composition 1510 that comprises an IEM. Also present in system 1500 is signal receiver 1520, such as the signal receiver illustrated in FIGS. 10 to 12. Signal receiver 1520 is configured to detect a signal emitted from the identifier of the IEM 1510. Signal receiver 1520 also includes physiologic sensing capability, such as ECG and movement sensing capability. Signal receiver 1520 is configured to transmit data to a patient's an external device or PDA 1530 (such as a smart phone or other wireless communication enabled device), which in turn transmits the data to a server 1540. Server 1540 may be configured as desired, e.g., to provide for patient directed permissions. For example, server 1540 may be configured to allow a family caregiver 1550 to participate in the patient's therapeutic regimen, e.g., via an interface (such as a web interface) that allows the family caregiver 1550 to monitor alerts and trends generated by the server 1540, and provide support back to the patient, as indicated by arrow 1560. The server 1540 may also be configured to provide responses directly to the patient, e.g., in the form of patient alerts, patient incentives, etc., as indicated by arrow 1565 which are relayed to the patient via PDA 1530. Server 1540 may also interact with a health care professional (e.g., RN, physician) 1555, which can use data processing algorithms to obtain measures of patient health and compliance, e.g., wellness index summaries, alerts, cross-patient benchmarks, etc., and provide informed clinical communication and support back to the patient, as indicated by arrow 1580.


Another example of the system of the present invention is shown in FIG. 18B. FIG. 18B depicts a system that includes a syringe 15107, a receiver 15105, a glucometer 15110, a wireless communication unit 15115, communication links 15150B-E, and a dosage manager 15160. The system generally provides intelligent mechanisms for controlling the delivery of a dosage by the syringe 15107 (e.g., subcutaneous needle insertion or luer connection with an Intra Venous access device). This control may include, for example, detecting that the syringe 15107 is proximate to the patient, measuring the amount of the dose administered by the syringe 15107, communicating the measurement information to other devices, such as the receiver 15105, the glucometer 15110, the wireless devices 15115, and/or the dosage manager 15160, and providing feedback information to one or more of those devices. In some implementations, the feedback information may prevent the administration of the dosage to the patient using, for example, an interlock at the syringe 15107 to prevent giving the dosage. The syringe 15107 may, based on the feedback, output a visual indication (e.g., a light emitting diode (LED)) or an aural signal to indicate that the dosage is not to be administered to the patient. For example, the interlock mechanism, LED, and/or sound at the syringe 15107 may signal that the patient is receiving the wrong type of medication, receiving the dosage at the wrong time, and/or receiving the wrong amount of medication.


In some implementations, the syringe 15107 may be configured in an interlock mode as a default state to prevent the administration of a dosage until the dosage manager 15160 provides feedback information to unlock the syringe 15107 to allow the administration of the agent or medication.


Moreover, the syringe 15107 may, in some embodiments, include a measurement mechanism to provide measurement information representative of the amount of the dosage. When that is the case, the measurement information may be used by the dosage manager 160 along with other patient information, such as blood pressure, glucose level, heart rate, ingestible event marker (IEM) data, etc., to control when, and/or how much of, a dosage is provided to the patient. Furthermore, the syringe 15107 may activate the measurement mechanism (which provides the measured information) when the syringe 15107 is proximate to (e.g., enters or is close to) the patient's body, at which time the measurement information and other information, such as an identifier associated with the syringe 15107, a patient identifier, etc, are carried by a signal to other devices, such as the receiver 15105, the glucometer 15110, and/or the wireless device 15115, for communication to the dosage manager 15160. Moreover, these other devices may monitor the time when the dosage is administered by the syringe 15107. As such, the dosage manager 15160 may receive a precise time when the dosage is administered rather than rely on user-provided dosage administration times. As such, the system may be used to evaluate a specific fluid transfer event between a parenteral fluid delivery device, such as syringe 15107, and a patient


While various details have been set forth in the foregoing description, it will be appreciated that the various aspects of the personal authentication apparatus, system, and method may be practiced without these specific details. For example, for conciseness and clarity selected aspects have been shown in block diagram form rather than in detail. Some portions of the detailed descriptions provided herein may be presented in terms of instructions that operate on data that is stored in a computer memory. Such descriptions and representations are used by those skilled in the art to describe and convey the substance of their work to others skilled in the art. In general, an algorithm refers to a self-consistent sequence of steps leading to a desired result, where a “step” refers to a manipulation of physical quantities which may, though need not necessarily, take the form of electrical or magnetic signals capable of being stored, transferred, combined, compared, and otherwise manipulated. It is common usage to refer to these signals as bits, values, elements, symbols, characters, terms, numbers, or the like. These and similar terms may be associated with the appropriate physical quantities and are merely convenient labels applied to these quantities.


Unless specifically stated otherwise as apparent from the foregoing discussion, it is appreciated that, throughout the foregoing description, discussions using terms such as “processing” or “computing” or “calculating” or “determining” or “displaying” or the like, refer to the action and processes of a computer system, or similar electronic computing device, that manipulates and transforms data represented as physical (electronic) quantities within the computer system's registers and memories into other data similarly represented as physical quantities within the computer system memories or registers or other such information storage, transmission or display devices.


It is worthy to note that any reference to “one aspect,” “an aspect,” “one embodiment,” or “an embodiment” means that a particular feature, structure, or characteristic described in connection with the aspect is included in at least one aspect. Thus, appearances of the phrases “in one aspect,” “in an aspect,” “in one embodiment,” or “in an embodiment” in various places throughout the specification are not necessarily all referring to the same aspect. Furthermore, the particular features, structures or characteristics may be combined in any suitable manner in one or more aspects.


Some aspects may be described in accordance with the expression “coupled” and “connected” along with their derivatives. It should be understood that these terms are not intended as synonyms for each other. For example, some aspects may be described using the term “connected” to indicate that two or more elements are in direct physical or electrical contact with each other. In another example, some aspects may be described using the term “coupled” to indicate that two or more elements are in direct physical or electrical contact. The term “coupled,” however, also may mean that two or more elements are not in direct contact with each other, but yet still co-operate or interact with each other.


It is worthy to note that any reference to “one aspect,” “an aspect,” “one embodiment,” or “an embodiment” means that a particular feature, structure, or characteristic described in connection with the aspect is included in at least one aspect. Thus, appearances of the phrases “in one aspect,” “in an aspect,” “in one embodiment,” or “in an embodiment” in various places throughout the specification are not necessarily all referring to the same aspect. Furthermore, the particular features, structures or characteristics may be combined in any suitable manner in one or more aspects.


Although various embodiments have been described herein, many modifications, variations, substitutions, changes, and equivalents to those embodiments may be implemented and will occur to those skilled in the art. Also, where materials are disclosed for certain components, other materials may be used. It is therefore to be understood that the foregoing description and the appended claims are intended to cover all such modifications and variations as falling within the scope of the disclosed embodiments. The following claims are intended to cover all such modification and variations.


In a general sense, those skilled in the art will recognize that the various aspects described herein which can be implemented, individually and/or collectively, by a wide range of hardware, software, firmware, or any combination thereof can be viewed as being composed of various types of “electrical circuitry.” Consequently, as used herein “electrical circuitry” includes, but is not limited to, electrical circuitry having at least one discrete electrical circuit, electrical circuitry having at least one integrated circuit, electrical circuitry having at least one application specific integrated circuit, electrical circuitry forming a general purpose computing device configured by a computer program (e.g., a general purpose computer configured by a computer program which at least partially carries out processes and/or devices described herein, or a microprocessor configured by a computer program which at least partially carries out processes and/or devices described herein), electrical circuitry forming a memory device (e.g., forms of random access memory), and/or electrical circuitry forming a communications device (e.g., a modem, communications switch, or optical-electrical equipment). Those having skill in the art will recognize that the subject matter described herein may be implemented in an analog or digital fashion or some combination thereof.


The foregoing detailed description has set forth various embodiments of the devices and/or processes via the use of block diagrams, flowcharts, and/or examples. Insofar as such block diagrams, flowcharts, and/or examples contain one or more functions and/or operations, it will be understood by those within the art that each function and/or operation within such block diagrams, flowcharts, or examples can be implemented, individually and/or collectively, by a wide range of hardware, software, firmware, or virtually any combination thereof. In one embodiment, several portions of the subject matter described herein may be implemented via Application Specific Integrated Circuits (ASICs), Field Programmable Gate Arrays (FPGAs), digital signal processors (DSPs), or other integrated formats. However, those skilled in the art will recognize that some aspects of the embodiments disclosed herein, in whole or in part, can be equivalently implemented in integrated circuits, as one or more computer programs running on one or more computers (e.g., as one or more programs running on one or more computer systems), as one or more programs running on one or more processors (e.g., as one or more programs running on one or more microprocessors), as firmware, or as virtually any combination thereof, and that designing the circuitry and/or writing the code for the software and or firmware would be well within the skill of one of skill in the art in light of this disclosure. In addition, those skilled in the art will appreciate that the mechanisms of the subject matter described herein are capable of being distributed as a program product in a variety of forms, and that an illustrative embodiment of the subject matter described herein applies regardless of the particular type of signal bearing medium used to actually carry out the distribution. Examples of a signal bearing medium include, but are not limited to, the following: a recordable type medium such as a floppy disk, a hard disk drive, a Compact Disc (CD), a Digital Video Disk (DVD), a digital tape, a computer memory, etc.; and a transmission type medium such as a digital and/or an analog communication medium (e.g., a fiber optic cable, a waveguide, a wired communications link, a wireless communication link (e.g., transmitter, receiver, transmission logic, reception logic, etc.), etc.).


All of the above-mentioned U.S. patents, U.S. patent application publications, U.S. patent applications, foreign patents, foreign patent applications, non-patent publications referred to in this specification and/or listed in any Application Data Sheet, or any other disclosure material are incorporated herein by reference, to the extent not inconsistent herewith. As such, and to the extent necessary, the disclosure as explicitly set forth herein supersedes any conflicting material incorporated herein by reference. Any material, or portion thereof, that is said to be incorporated by reference herein, but which conflicts with existing definitions, statements, or other disclosure material set forth herein will only be incorporated to the extent that no conflict arises between that incorporated material and the existing disclosure material.


One skilled in the art will recognize that the herein described components (e.g., operations), devices, objects, and the discussion accompanying them are used as examples for the sake of conceptual clarity and that various configuration modifications are contemplated. Consequently, as used herein, the specific exemplars set forth and the accompanying discussion are intended to be representative of their more general classes. In general, use of any specific exemplar is intended to be representative of its class, and the non-inclusion of specific components (e.g., operations), devices, and objects should not be taken limiting.


With respect to the use of substantially any plural and/or singular terms herein, those having skill in the art can translate from the plural to the singular and/or from the singular to the plural as is appropriate to the context and/or application. The various singular/plural permutations are not expressly set forth herein for sake of clarity.


The herein described subject matter sometimes illustrates different components contained within, or connected with, different other components. It is to be understood that such depicted architectures are merely exemplary, and that in fact many other architectures may be implemented which achieve the same functionality. In a conceptual sense, any arrangement of components to achieve the same functionality is effectively “associated” such that the desired functionality is achieved. Hence, any two components herein combined to achieve a particular functionality can be seen as “associated with” each other such that the desired functionality is achieved, irrespective of architectures or intermedial components. Likewise, any two components so associated can also be viewed as being “operably connected,” or “operably coupled,” to each other to achieve the desired functionality, and any two components capable of being so associated can also be viewed as being “operably couplable,” to each other to achieve the desired functionality. Specific examples of operably couplable include but are not limited to physically mateable and/or physically interacting components, and/or wirelessly interactable, and/or wirelessly interacting components, and/or logically interacting, and/or logically interactable components.


In some instances, one or more components may be referred to herein as “configured to,” “configurable to,” “operable/operative to,” “adapted/adaptable,” “able to,” “conformable/conformed to,” etc. Those skilled in the art will recognize that “configured to” can generally encompass active-state components and/or inactive-state components and/or standby-state components, unless context requires otherwise.


While particular aspects of the present subject matter described herein have been shown and described, it will be apparent to those skilled in the art that, based upon the teachings herein, changes and modifications may be made without departing from the subject matter described herein and its broader aspects and, therefore, the appended claims are to encompass within their scope all such changes and modifications as are within the true spirit and scope of the subject matter described herein. It will be understood by those within the art that, in general, terms used herein, and especially in the appended claims (e.g., bodies of the appended claims) are generally intended as “open” terms (e.g., the term “including” should be interpreted as “including but not limited to,” the term “having” should be interpreted as “having at least,” the term “includes” should be interpreted as “includes but is not limited to,” etc.). It will be further understood by those within the art that if a specific number of an introduced claim recitation is intended, such an intent will be explicitly recited in the claim, and in the absence of such recitation no such intent is present. For example, as an aid to understanding, the following appended claims may contain usage of the introductory phrases “at least one” and “one or more” to introduce claim recitations. However, the use of such phrases should not be construed to imply that the introduction of a claim recitation by the indefinite articles “a” or “an” limits any particular claim containing such introduced claim recitation to claims containing only one such recitation, even when the same claim includes the introductory phrases “one or more” or “at least one” and indefinite articles such as “a” or “an” (e.g., “a” and/or “an” should typically be interpreted to mean “at least one” or “one or more”); the same holds true for the use of definite articles used to introduce claim recitations.


In addition, even if a specific number of an introduced claim recitation is explicitly recited, those skilled in the art will recognize that such recitation should typically be interpreted to mean at least the recited number (e.g., the bare recitation of “two recitations,” without other modifiers, typically means at least two recitations, or two or more recitations). Furthermore, in those instances where a convention analogous to “at least one of A, B, and C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, and C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). In those instances where a convention analogous to “at least one of A, B, or C, etc.” is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g., “a system having at least one of A, B, or C” would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). It will be further understood by those within the art that typically a disjunctive word and/or phrase presenting two or more alternative terms, whether in the description, claims, or drawings, should be understood to contemplate the possibilities of including one of the terms, either of the terms, or both terms unless context dictates otherwise. For example, the phrase “A or B” will be typically understood to include the possibilities of “A” or “B” or “A and B.”


With respect to the appended claims, those skilled in the art will appreciate that recited operations therein may generally be performed in any order. Also, although various operational flows are presented in a sequence(s), it should be understood that the various operations may be performed in other orders than those which are illustrated, or may be performed concurrently. Examples of such alternate orderings may include overlapping, interleaved, interrupted, reordered, incremental, preparatory, supplemental, simultaneous, reverse, or other variant orderings, unless context dictates otherwise. Furthermore, terms like “responsive to,” “related to,” or other past-tense adjectives are generally not intended to exclude such variants, unless context dictates otherwise.


In certain cases, use of a system or method may occur in a territory even if components are located outside the territory. For example, in a distributed computing context, use of a distributed computing system may occur in a territory even though parts of the system may be located outside of the territory (e.g., relay, server, processor, signal-bearing medium, transmitting computer, receiving computer, etc. located outside the territory).


A sale of a system or method may likewise occur in a territory even if components of the system or method are located and/or used outside the territory. Further, implementation of at least part of a system for performing a method in one territory does not preclude use of the system in another territory.


Although various embodiments have been described herein, many modifications, variations, substitutions, changes, and equivalents to those embodiments may be implemented and will occur to those skilled in the art. Also, where materials are disclosed for certain components, other materials may be used. It is therefore to be understood that the foregoing description and the appended claims are intended to cover all such modifications and variations as falling within the scope of the disclosed embodiments. The following claims are intended to cover all such modification and variations.


In summary, numerous benefits have been described which result from employing the concepts described herein. The foregoing description of the one or more embodiments has been presented for purposes of illustration and description. It is not intended to be exhaustive or limiting to the precise form disclosed. Modifications or variations are possible in light of the above teachings. The one or more embodiments were chosen and described in order to illustrate principles and practical application to thereby enable one of ordinary skill in the art to utilize the various embodiments and with various modifications as are suited to the particular use contemplated. It is intended that the claims submitted herewith define the overall scope.

Claims
  • 1. A system, comprising: an enclosing arrangement apparatus configured to house and detach from a mobile device and to conductively couple to a body of a patient, the enclosing arrangement apparatus comprising: at least one electrode configured to contact the body of the patient and receive an electrically conductive signal transmitting through the patient;a detection circuit electrically coupled to the at least one electrode and configured to detect the electrically conductive signal transmitted to the at least one electrode; anda docking station comprising: at least a partial cavity shaped to house the mobile device when the mobile device is docked in the docking station; anda connector comprising one or more electrical leads and configured to couple the mobile device to the enclosing arrangement apparatus, and to electrically and communicatively connect the mobile device to the detection circuit when the mobile device is docked in the docking station;wherein the mobile device is electrically and communicatively disconnected from the enclosing arrangement apparatus when the mobile device is undocked from the docking station; andan authentication receiver module configured to be stored in the mobile device and to access the electrically conductive signal through the connector and to authenticate an identity of the patient when the electrically conductive signal matches a predetermined criterion;wherein the electrically conductive signal includes a profile of biometric signals including heart rate, body temperature, and circadian rhythm detectable by the at least one electrode.
  • 2. The system of claim 1, wherein the authentication receiver module is configured to store a non-physiological secret code.
  • 3. The system of claim 2, wherein the electrically conductive signal comprises the profile of biometric signals hashed with the non-physiological secret code to yield a signature.
  • 4. The system of claim 3, wherein the predetermined criterion includes a baseline biometric signature stored in a database comprising a running average of previously detected biometric signals including heart rate, body temperature, and circadian rhythm received by the physiological sensing module as a running series of signatures generated by the body associated device, each signature in the running series including a different profile of biometric signals including heart rate, body temperature, and circadian rhythm to be used to calculate the running average.
  • 5. The system of claim 1, further comprising a transbody conductive communication module stored in the mobile device and configured to access the electrically conductive signal representing an authentication code for the mobile device.
  • 6. The system of claim 5, wherein the enclosing arrangement apparatus is configured to transmit the authentication code to the mobile device a predetermined number of times, and wherein the enclosing arrangement apparatus is configured to be de-authorized and to stop transmitting the authentication code after it has transmitted the authentication code the predetermined number of times.
  • 7. The system of claim 1, further comprising a decoder stored in the mobile device and configured to decode the detected electrically conductive signal.
  • 8. The system of claim 7, further comprising a compare module stored in the mobile device and configured to compare the decoded detected electrically conductive signal with established criteria.
  • 9. The system of claim 1, wherein the enclosing arrangement apparatus is configured to transmit the electrically conductive signal when an ingestible event marker system is activated inside the body of the patient.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a Continuation-in-part of application Ser. No. 13/336,956, filed Dec. 23, 2011, which is a Divisional Application of Ser. No. 12/673,326, filed Feb. 12, 2010, which application claims benefit of U.S. 371 National Phase of PCT/US09/68128, filed Dec. 15, 2009, which application claims the benefit of Provisional Application 61/122,723, filed Dec. 15, 2008, which application claims the benefit of Provisional Application 61/160,289, filed Mar. 13, 2009, which application claims the benefit of Provisional Application 61/240,571, filed Sep. 8, 2009, which application claims the benefit of Provisional Application 61/251,088, filed Oct. 13, 2009, the disclosures of which applications are herein incorporated by reference. This application is a Continuation-in-part of Application PCT/US2012/047076 filed Jul. 17, 2012, which application claims the benefit of Provisional Application 61/510,434 filed Jul. 21, 2011, the disclosures of which applications are herein incorporated by reference.

US Referenced Citations (933)
Number Name Date Kind
2206695 Guanella Jul 1940 A
2463504 Atkins Mar 1949 A
2582968 Deloraine et al. Jan 1952 A
3340866 Noller Sep 1967 A
3607788 Adolph Sep 1971 A
3642008 Bolduc Feb 1972 A
3679480 Brown et al. Jul 1972 A
3682160 Murata Aug 1972 A
3719183 Schwartz Mar 1973 A
3828766 Krasnow Aug 1974 A
3837339 Aisenberg et al. Sep 1974 A
3989050 Buchalter Nov 1976 A
4067014 Wheeler et al. Jan 1978 A
4077397 Ellis Mar 1978 A
4077398 Ellis Mar 1978 A
4082087 Howson Apr 1978 A
4090752 Long May 1978 A
4106348 Auphan Aug 1978 A
4121573 Crovella et al. Oct 1978 A
4129125 Lester Dec 1978 A
4149168 Hose Apr 1979 A
4166453 McClelland Sep 1979 A
4185172 Melindo et al. Jan 1980 A
4239046 Ong Dec 1980 A
4269189 Abraham May 1981 A
4331654 Morris May 1982 A
4333150 Matty et al. Jun 1982 A
4345588 Widder et al. Aug 1982 A
4418697 Tama Dec 1983 A
4425117 Hugemann Jan 1984 A
4494950 Fischell Jan 1985 A
4513385 Muri Apr 1985 A
4559950 Vaughan Dec 1985 A
4578061 Lemelson Mar 1986 A
4635641 Hoffman Jan 1987 A
4654165 Eisenber Mar 1987 A
4669479 Dunseath Jun 1987 A
4688400 Chioffe Aug 1987 A
4725997 Urquhart et al. Feb 1988 A
4749575 Rotman et al. Jun 1988 A
4763659 Dunseath Aug 1988 A
4784162 Ricks Nov 1988 A
4793825 Benjamin Dec 1988 A
4809705 Ascher Mar 1989 A
4844076 Lesho Jul 1989 A
4858617 Sanders Aug 1989 A
4896261 Nolan Jan 1990 A
4975230 Pinkhasov Dec 1990 A
4987897 Funke Jan 1991 A
5016634 Vock et al. May 1991 A
5079006 Urguhart Jan 1992 A
5113859 Funke May 1992 A
5167626 Casper Dec 1992 A
5176626 Soehendra Jan 1993 A
5232383 Barnick Aug 1993 A
5245332 Katzenstein et al. Sep 1993 A
5261402 DiSabito Nov 1993 A
5263481 Axelgaard et al. Nov 1993 A
5281287 Lloyd Jan 1994 A
5283136 Peled et al. Feb 1994 A
5288564 Klein Feb 1994 A
5318557 Gross Jun 1994 A
5394882 Mawhinney Mar 1995 A
5458141 Neil et al. Oct 1995 A
5473612 Dehner, Jr. et al. Dec 1995 A
5485841 Watkin et al. Jan 1996 A
5511548 Riazzi et al. Apr 1996 A
5551020 Flax et al. Aug 1996 A
5596302 Mastrocola et al. Jan 1997 A
D377983 Sabri et al. Feb 1997 S
5623520 Kaiser Apr 1997 A
5634466 Gruner Jun 1997 A
5634468 Platt Jun 1997 A
5645063 Straka et al. Jul 1997 A
5720771 Snell Feb 1998 A
5724432 Bouvet et al. Mar 1998 A
5740811 Hedberg Apr 1998 A
5792048 Schaefer Aug 1998 A
5802467 Salazar Sep 1998 A
5833716 Bar-Or Nov 1998 A
5845265 Woolston Dec 1998 A
5862803 Besson Jan 1999 A
5862808 Albarello Jan 1999 A
5868136 Fox Feb 1999 A
5921925 Cartmell et al. Jul 1999 A
5925030 Gross et al. Jul 1999 A
5925066 Kroll et al. Jul 1999 A
5937059 Kim et al. Aug 1999 A
5957854 Besson et al. Sep 1999 A
5974124 Schlueter, Jr. et al. Oct 1999 A
5981166 Mandecki Nov 1999 A
5999846 Pardey et al. Dec 1999 A
6023631 Cartmell et al. Feb 2000 A
6033370 Reinbold Mar 2000 A
6038464 Axelgaard et al. Mar 2000 A
6042710 Dubrow Mar 2000 A
6047203 Sackner Apr 2000 A
6076016 Feierbach Jun 2000 A
6081734 Batz Jun 2000 A
6095985 Raymond et al. Aug 2000 A
6115636 Ryan Sep 2000 A
6117077 Del Mar et al. Sep 2000 A
6122351 Schlueter, Jr. et al. Sep 2000 A
6141592 Pauly Oct 2000 A
6151353 Harrison et al. Nov 2000 A
6200265 Walsh et al. Mar 2001 B1
6200625 Beckett Mar 2001 B1
6204764 Maloney Mar 2001 B1
6206702 Hayden et al. Mar 2001 B1
6217744 Crosby Apr 2001 B1
6231593 Meserol May 2001 B1
6238338 DeLuca et al. May 2001 B1
6245057 Sieben et al. Jun 2001 B1
6275476 Wood Aug 2001 B1
6285897 Kilcoyne et al. Sep 2001 B1
6287252 Lugo Sep 2001 B1
6289238 Besson et al. Sep 2001 B1
6301298 Kuntz et al. Oct 2001 B1
6315719 Rode et al. Nov 2001 B1
6317714 Del Castillo Nov 2001 B1
6327486 Nissila et al. Dec 2001 B1
6358202 Arent Mar 2002 B1
6364834 Reuss Apr 2002 B1
6366206 Ishikawa et al. Apr 2002 B1
6371927 Brune Apr 2002 B1
6374670 Spelman Apr 2002 B1
6380858 Yarin et al. Apr 2002 B1
6394953 Devlin et al. May 2002 B1
6394997 Lemelson May 2002 B1
6409674 Brockway et al. Jun 2002 B1
6426863 Munshi Jul 2002 B1
6432292 Pinto et al. Aug 2002 B1
6440069 Raymond et al. Aug 2002 B1
6441747 Khair Aug 2002 B1
6477424 Thompson et al. Nov 2002 B1
6482156 Lliff Nov 2002 B2
6494829 New et al. Dec 2002 B1
6496705 Ng et al. Dec 2002 B1
6526315 Inagawa Feb 2003 B1
6544174 West Apr 2003 B2
6564079 Cory May 2003 B1
6577893 Besson et al. Jun 2003 B1
6579231 Phipps Jun 2003 B1
6605038 Teller et al. Aug 2003 B1
6605046 Del Mar Aug 2003 B1
6609018 Cory Aug 2003 B2
6612984 Kerr Sep 2003 B1
6632175 Marshall Oct 2003 B1
6632216 Houzego et al. Oct 2003 B2
6643541 Mok et al. Nov 2003 B2
6654638 Sweeney Nov 2003 B1
6663846 McCombs Dec 2003 B1
6673474 Yamamoto Jan 2004 B2
6680923 Leon Jan 2004 B1
6689117 Sweeney et al. Feb 2004 B2
6694161 Mehrotra Feb 2004 B2
6704602 Berg et al. Mar 2004 B2
6720923 Hayward et al. Apr 2004 B1
6738671 Christophersom et al. May 2004 B2
6740033 Olejniczak et al. May 2004 B1
6745082 Axelgaard et al. Jun 2004 B2
6755783 Cosentino Jun 2004 B2
6757523 Fry Jun 2004 B2
6800060 Marshall Oct 2004 B2
6801137 Eggers et al. Oct 2004 B2
6807438 Brun Del Re et al. Oct 2004 B1
6814706 Barton et al. Nov 2004 B2
6822554 Vrijens et al. Nov 2004 B2
6836862 Erekson et al. Dec 2004 B1
6839659 Tarassenko et al. Jan 2005 B2
6840904 Goldberg Jan 2005 B2
6842636 Perrault Jan 2005 B2
6845272 Thomsen Jan 2005 B1
6856832 Matsumura et al. Feb 2005 B1
6864780 Doi Mar 2005 B2
6879810 Bouet Apr 2005 B2
6882881 Lesser et al. Apr 2005 B1
6889165 Lind et al. May 2005 B2
6897788 Khair et al. May 2005 B2
6909878 Haller Jun 2005 B2
6922592 Thompson et al. Jul 2005 B2
6928370 Anuzis et al. Aug 2005 B2
6929636 Von Alten Aug 2005 B1
6937150 Medema Aug 2005 B2
6942616 Kerr Sep 2005 B2
6951536 Yokoi Oct 2005 B2
6956917 Lenosky Oct 2005 B2
6957107 Rogers et al. Oct 2005 B2
6959929 Pugnet et al. Nov 2005 B2
6961601 Mathews et al. Nov 2005 B2
6968153 Heinonen Nov 2005 B1
6987965 Ng et al. Jan 2006 B2
6990082 Zehavi et al. Jan 2006 B1
7002476 Rapchak Feb 2006 B2
7004395 Koenck Feb 2006 B2
7009634 Iddan et al. Mar 2006 B2
7009946 Kardach Mar 2006 B1
7013162 Gorsuch Mar 2006 B2
7016648 Haller Mar 2006 B2
7020508 Stivoric Mar 2006 B2
7024248 Penner et al. Apr 2006 B2
7031745 Shen Apr 2006 B2
7031857 Tarassenko et al. Apr 2006 B2
7039453 Mullick May 2006 B2
7046649 Awater et al. May 2006 B2
7076437 Levy Jul 2006 B1
7116252 Teraguchi Oct 2006 B2
7118531 Krill Oct 2006 B2
7127300 Mazar Oct 2006 B2
7139332 Yu et al. Nov 2006 B2
7146228 Nielsen Dec 2006 B2
7146449 Do et al. Dec 2006 B2
7148828 Fernandez Dec 2006 B2
7149581 Goedeke Dec 2006 B2
7154071 Sattler et al. Dec 2006 B2
7154816 Soloff Dec 2006 B2
7155232 Godfrey et al. Dec 2006 B2
7160258 Imran Jan 2007 B2
7161484 Tsoukalis Jan 2007 B2
7164942 Avrahami Jan 2007 B2
7171166 Ng et al. Jan 2007 B2
7171177 Park et al. Jan 2007 B2
7171259 Rytky Jan 2007 B2
7187960 Abreu Mar 2007 B2
7188767 Penuela Mar 2007 B2
7194038 Inkinen Mar 2007 B1
7206630 Tarler Apr 2007 B1
7209790 Thompson et al. Apr 2007 B2
7215660 Perlman May 2007 B2
7215991 Besson May 2007 B2
7218867 Bergelson May 2007 B2
7231451 Law Jun 2007 B2
7243118 Lou Jul 2007 B2
7246521 Kim Jul 2007 B2
7249212 Do Jul 2007 B2
7252792 Perrault Aug 2007 B2
7253716 Lovoi et al. Aug 2007 B2
7261690 Teller Aug 2007 B2
7270633 Goscha Sep 2007 B1
7273454 Raymond et al. Sep 2007 B2
7283867 Strother et al. Oct 2007 B2
7285090 Stivoric et al. Oct 2007 B2
7289855 Nghiem Oct 2007 B2
7291497 Holmes Nov 2007 B2
7292139 Mazar et al. Nov 2007 B2
7294105 Islam Nov 2007 B1
7311665 Hawthorne Dec 2007 B2
7313163 Liu Dec 2007 B2
7317378 Jarvis et al. Jan 2008 B2
7318808 Tarassenko et al. Jan 2008 B2
7336929 Yasuda Feb 2008 B2
7342895 Serpa Mar 2008 B2
7346380 Axelgaard et al. Mar 2008 B2
7349722 Witkowski et al. Mar 2008 B2
7352998 Palin Apr 2008 B2
7353258 Washburn Apr 2008 B2
7357891 Yang et al. Apr 2008 B2
7359674 Markki Apr 2008 B2
7366558 Virtanen et al. Apr 2008 B2
7373196 Ryu et al. May 2008 B2
7375739 Robbins May 2008 B2
7376435 McGowan May 2008 B2
7382247 Welch et al. Jun 2008 B2
7382263 Danowski et al. Jun 2008 B2
7387607 Holt Jun 2008 B2
7388903 Godfrey et al. Jun 2008 B2
7389088 Kim Jun 2008 B2
7392015 Farlow Jun 2008 B1
7395105 Schmidt et al. Jul 2008 B2
7395106 Ryu et al. Jul 2008 B2
7396330 Banet Jul 2008 B2
7404968 Abrams et al. Jul 2008 B2
7413544 Kerr Aug 2008 B2
7414534 Kroll et al. Aug 2008 B1
7415242 Ngan Aug 2008 B1
7424268 Diener Sep 2008 B2
7424319 Muehisteff Sep 2008 B2
7427266 Ayer et al. Sep 2008 B2
7471665 Perlman Dec 2008 B2
7476104 Marmaropoulos et al. Jan 2009 B2
7499674 Salokannel Mar 2009 B2
7502643 Farringdon Mar 2009 B2
7505795 Lim et al. Mar 2009 B1
7510121 Koenck Mar 2009 B2
7512448 Malick Mar 2009 B2
7515043 Welch Apr 2009 B2
7523756 Minai Apr 2009 B2
7525426 Edelstein Apr 2009 B2
7539533 Tran May 2009 B2
7542878 Nanikashvili Jun 2009 B2
7547278 Miyazaki et al. Jun 2009 B2
7551590 Halier Jun 2009 B2
7554452 Cole Jun 2009 B2
7575005 Mumford Aug 2009 B2
7599003 Suzuki et al. Oct 2009 B2
7616111 Covannon Nov 2009 B2
7616710 Kim et al. Nov 2009 B2
7617001 Penner et al. Nov 2009 B2
7626387 Adachi Dec 2009 B2
7640802 King et al. Jan 2010 B2
7647112 Tracey Jan 2010 B2
7647185 Tarassenko et al. Jan 2010 B2
7653031 Godfrey et al. Jan 2010 B2
7668437 Yamada et al. Feb 2010 B1
7672703 Yeo et al. Mar 2010 B2
7672714 Kuo Mar 2010 B2
7673679 Harrison et al. Mar 2010 B2
7678043 Gilad Mar 2010 B2
7688204 Yamanaka et al. Mar 2010 B2
7689437 Teller et al. Mar 2010 B1
7697994 VanDanacker et al. Apr 2010 B2
7720036 Sadri May 2010 B2
7729776 Von Arx et al. Jun 2010 B2
7733224 Tran Jun 2010 B2
7736318 Costentino Jun 2010 B2
7750790 Yang et al. Jul 2010 B2
7756587 Penner et al. Jul 2010 B2
7782991 Sobchak et al. Aug 2010 B2
7797033 D'Andrea et al. Sep 2010 B2
7809399 Lu Oct 2010 B2
7844341 Von Arx et al. Nov 2010 B2
7874993 Bardy Jan 2011 B2
7885700 Clark Feb 2011 B2
7904133 Gehman et al. Mar 2011 B2
D639437 Bishay et al. Jun 2011 S
7978064 Zdebiick et al. Jul 2011 B2
7983189 Bugenhagen Jul 2011 B2
8036748 Zdeblick et al. Oct 2011 B2
8055334 Savage et al. Nov 2011 B2
8073707 Teller et al. Dec 2011 B2
8083128 Dembo et al. Dec 2011 B2
8094807 Ishibashi et al. Jan 2012 B2
8114021 Robertson et al. Feb 2012 B2
8123576 Kim Feb 2012 B2
8140143 Picard et al. Mar 2012 B2
8160672 Kim Apr 2012 B2
8170515 Le Reverend et al. May 2012 B2
8177611 Kang May 2012 B2
8180425 Selvitelli et al. May 2012 B2
8184854 Bartsch May 2012 B2
8185191 Shapiro et al. May 2012 B1
8185646 Headley May 2012 B2
8190230 Rytky May 2012 B2
8193821 Mueller Jun 2012 B2
8200320 Kovacs Jun 2012 B2
8214007 Baker et al. Jul 2012 B2
8238998 Park Aug 2012 B2
8249686 Libbus et al. Aug 2012 B2
8253586 Matak Aug 2012 B1
8254853 Rofougaran Aug 2012 B2
8285356 Bly et al. Oct 2012 B2
8290574 Felid et al. Oct 2012 B2
8301232 Albert et al. Oct 2012 B2
8308640 Baldus et al. Nov 2012 B2
8315687 Cross et al. Nov 2012 B2
8321672 Asano Nov 2012 B2
8332009 McLaughlin et al. Dec 2012 B2
8360976 Imran Jan 2013 B2
8369936 Farringdon et al. Feb 2013 B2
8386009 Lindberg et al. Feb 2013 B2
8404275 Habboushe Mar 2013 B2
8440274 Wang May 2013 B2
8454528 Yuen et al. Jun 2013 B2
8471960 Lin et al. Jun 2013 B2
8514979 Laporte Aug 2013 B2
8515559 Roberts Aug 2013 B2
8538544 Sivard Sep 2013 B2
8545436 Robertson et al. Oct 2013 B2
8548033 Nemeth et al. Oct 2013 B2
8604974 Ganeshan Dec 2013 B2
8615290 Lin et al. Dec 2013 B2
8620402 Parker, III et al. Dec 2013 B2
8634838 Hellwig et al. Jan 2014 B2
8660645 Stevenson et al. Feb 2014 B2
8668643 Kinast Mar 2014 B2
8725243 Dilorenzo et al. May 2014 B2
8730031 Thompson et al. May 2014 B2
8754799 Coln et al. Jun 2014 B2
8773258 Vosch et al. Jul 2014 B2
8836513 Hafezi et al. Sep 2014 B2
8838217 Myr Sep 2014 B2
8858432 Robertson Oct 2014 B2
8886281 Pernu et al. Nov 2014 B2
8886316 Juels Nov 2014 B1
8892194 Balji et al. Nov 2014 B2
8908943 Berry et al. Dec 2014 B2
8920345 Greenberg Dec 2014 B2
8923956 Clark et al. Dec 2014 B2
8926509 Magar et al. Jan 2015 B2
8932221 Colliou et al. Jan 2015 B2
8945005 Hafezi et al. Feb 2015 B2
8945328 Longinotti et al. Feb 2015 B2
8989837 Weinstein et al. Mar 2015 B2
9014779 Zdeblick et al. Apr 2015 B2
9031658 Chiao et al. May 2015 B2
9149577 Robertson et al. Oct 2015 B2
9158890 Meredith et al. Oct 2015 B2
9189941 Eschelman et al. Nov 2015 B2
9226663 Fei Jan 2016 B2
9226679 Balda Jan 2016 B2
9270025 Robertson et al. Feb 2016 B2
9270503 Fleming et al. Feb 2016 B2
9277864 Yang et al. Mar 2016 B2
9320455 Hafezi et al. Apr 2016 B2
9439566 Arne et al. Sep 2016 B2
9439582 Berkman et al. Sep 2016 B2
9439599 Thompson et al. Sep 2016 B2
9517012 Lane et al. Dec 2016 B2
9577864 Kushner et al. Feb 2017 B2
9597010 Thompson et al. Mar 2017 B2
9659423 Robertson et al. May 2017 B2
9756874 Arne et al. Sep 2017 B2
9787511 Fleming et al. Oct 2017 B2
9820658 Tran Nov 2017 B2
9946297 Nazzaro et al. Apr 2018 B2
10498572 Flemming et al. Dec 2019 B2
20010027331 Thompson Oct 2001 A1
20010031071 Nichols et al. Oct 2001 A1
20010044588 Mault Nov 2001 A1
20010051766 Gazdzinski Dec 2001 A1
20010056262 Cabiri et al. Dec 2001 A1
20020002326 Causey et al. Jan 2002 A1
20020026111 Ackerman Feb 2002 A1
20020040278 Anuzis et al. Apr 2002 A1
20020077620 Sweeney et al. Jun 2002 A1
20020128934 Shaer Sep 2002 A1
20020132226 Nair Sep 2002 A1
20020169696 Zara Nov 2002 A1
20020192159 Reitberg Dec 2002 A1
20020193669 Glukhovsky Dec 2002 A1
20020198470 Imran et al. Dec 2002 A1
20030017826 Fishman Jan 2003 A1
20030023150 Yokoi et al. Jan 2003 A1
20030028226 Thompson Feb 2003 A1
20030065536 Hansen Apr 2003 A1
20030076179 Branch et al. Apr 2003 A1
20030083559 Thompson May 2003 A1
20030091121 Kenmochi May 2003 A1
20030126593 Mault Jul 2003 A1
20030130714 Nielsen et al. Jul 2003 A1
20030135128 Suffin et al. Jul 2003 A1
20030135392 Vrijens et al. Jul 2003 A1
20030182212 Say et al. Jul 2003 A1
20030182213 Say et al. Jul 2003 A1
20030152622 Louie-Helm et al. Aug 2003 A1
20030158466 Lynn et al. Aug 2003 A1
20030158756 Abramson Aug 2003 A1
20030162556 Libes Aug 2003 A1
20030164401 Andreasson et al. Sep 2003 A1
20030167000 Mullick et al. Sep 2003 A1
20030171791 KenKnight Sep 2003 A1
20030171898 Tarassenko et al. Sep 2003 A1
20030181788 Yokoi et al. Sep 2003 A1
20030181815 Ebner et al. Sep 2003 A1
20030185286 Yuen Oct 2003 A1
20030187337 Tarassenko et al. Oct 2003 A1
20030187338 Say et al. Oct 2003 A1
20030195403 Berner et al. Oct 2003 A1
20030208113 Mault et al. Nov 2003 A1
20030213495 Fujita et al. Nov 2003 A1
20030214579 Iddan Nov 2003 A1
20030216622 Meron et al. Nov 2003 A1
20030216625 Phipps Nov 2003 A1
20030216666 Ericson et al. Nov 2003 A1
20030216729 Marchitto Nov 2003 A1
20030229382 Sun et al. Dec 2003 A1
20040008123 Carrender et al. Jan 2004 A1
20040018476 LaDue Jan 2004 A1
20040019172 Yang et al. Jan 2004 A1
20040034295 Salganicoff Feb 2004 A1
20040049245 Gass Mar 2004 A1
20040064728 Scheurich Apr 2004 A1
20040073095 Causey et al. Apr 2004 A1
20040073454 Urquhart et al. Apr 2004 A1
20040077995 Ferek-Petric Apr 2004 A1
20040082982 Gord et al. Apr 2004 A1
20040087839 Raymond et al. May 2004 A1
20040092801 Drakulic May 2004 A1
20040106859 Say et al. Jun 2004 A1
20040115507 Potter et al. Jun 2004 A1
20040115517 Fukada et al. Jun 2004 A1
20040121015 Chidlaw et al. Jun 2004 A1
20040122297 Stahmann et al. Jun 2004 A1
20040148140 Tarassenko et al. Jul 2004 A1
20040153007 Harris Aug 2004 A1
20040165686 Siwiak Aug 2004 A1
20040167226 Serafini Aug 2004 A1
20040167801 Say et al. Aug 2004 A1
20040193020 Chiba Sep 2004 A1
20040193029 Gluhovsky Sep 2004 A1
20040193446 Mayer et al. Sep 2004 A1
20040199222 Sun et al. Oct 2004 A1
20040215084 Shimizu et al. Oct 2004 A1
20040218683 Batra Nov 2004 A1
20040220643 Schmidt Nov 2004 A1
20040224644 Wu Nov 2004 A1
20040225199 Evanyk Nov 2004 A1
20040240481 Matsumoto Dec 2004 A1
20040253304 Gross et al. Dec 2004 A1
20040260154 Sidelnik Dec 2004 A1
20050010338 Kraeling et al. Jan 2005 A1
20050017841 Doi Jan 2005 A1
20050020887 Goldberg Jan 2005 A1
20050021103 DiLorenzo Jan 2005 A1
20050021370 Riff Jan 2005 A1
20050024198 Ward Feb 2005 A1
20050027205 Tarassenko et al. Feb 2005 A1
20050038321 Fujita et al. Feb 2005 A1
20050041752 Rosen Feb 2005 A1
20050043634 Yokoi et al. Feb 2005 A1
20050055014 Coppeta et al. Mar 2005 A1
20050062644 Leci Mar 2005 A1
20050065407 Nakamura et al. Mar 2005 A1
20050070778 Lackey Mar 2005 A1
20050092108 Andermo May 2005 A1
20050096514 Starkebaum May 2005 A1
20050096562 Delalic et al. May 2005 A1
20050101843 Quinn May 2005 A1
20050101872 Sattler May 2005 A1
20050115561 Stahmann et al. Jun 2005 A1
20050116820 Goidreich Jun 2005 A1
20050117389 Worledge Jun 2005 A1
20050121322 Say et al. Jun 2005 A1
20050131281 Ayer et al. Jun 2005 A1
20050137480 Alt et al. Jun 2005 A1
20050143623 Kojima Jun 2005 A1
20050148883 Boesen Jul 2005 A1
20050154428 Bruinsma Jul 2005 A1
20050165323 Montgomery Jul 2005 A1
20050177069 Takizawa Aug 2005 A1
20050182389 LaPorte Aug 2005 A1
20050187789 Hatlestad et al. Aug 2005 A1
20050192489 Marshall Sep 2005 A1
20050197680 DelMain et al. Sep 2005 A1
20050228268 Cole Oct 2005 A1
20050234307 Heinonen Oct 2005 A1
20050240305 Bogash et al. Oct 2005 A1
20050245794 Dinsmoor Nov 2005 A1
20050259768 Yang et al. Nov 2005 A1
20050261559 Mumford Nov 2005 A1
20050267556 Shuros et al. Dec 2005 A1
20050267756 Schultz et al. Dec 2005 A1
20050277912 John Dec 2005 A1
20050277999 Strother et al. Dec 2005 A1
20050285746 Sengupta Dec 2005 A1
20050288594 Lewkowicz et al. Dec 2005 A1
20060001496 Abrosimov et al. Jan 2006 A1
20060036134 Tarassenko et al. Feb 2006 A1
20060061472 Lovoi et al. Mar 2006 A1
20060065713 Kingery Mar 2006 A1
20060074283 Henderson Apr 2006 A1
20060078765 Yang et al. Apr 2006 A1
20060095091 Drew May 2006 A1
20060095093 Bettesh et al. May 2006 A1
20060100533 Han May 2006 A1
20060109058 Keating May 2006 A1
20060110962 Powell May 2006 A1
20060122474 Teller et al. Jun 2006 A1
20060122667 Chavan et al. Jun 2006 A1
20060129060 Lee et al. Jun 2006 A1
20060136266 Tarassenko et al. Jun 2006 A1
20060136744 Lange Jun 2006 A1
20060142648 Banet Jun 2006 A1
20060145876 Kimura Jul 2006 A1
20060148254 McLean Jul 2006 A1
20060149339 Burnes Jul 2006 A1
20060155174 Glukhovsky et al. Jul 2006 A1
20060155183 Kroecker Jul 2006 A1
20060158820 Takiguchi Jul 2006 A1
20060161225 Sormann et al. Jul 2006 A1
20060179949 Kim Aug 2006 A1
20060183993 Horn Aug 2006 A1
20060184092 Atanasoska et al. Aug 2006 A1
20060204738 Dubrow et al. Sep 2006 A1
20060210626 Spaeder Sep 2006 A1
20060216603 Choi Sep 2006 A1
20060218011 Walker Sep 2006 A1
20060235489 Drew Oct 2006 A1
20060247505 Siddiqui Nov 2006 A1
20060253005 Drinan Nov 2006 A1
20060255064 Donaldson Nov 2006 A1
20060265246 Hoag Nov 2006 A1
20060268170 Suzuki et al. Nov 2006 A1
20060269019 Simmons et al. Nov 2006 A1
20060270346 Ibrahim Nov 2006 A1
20060277097 Shafron et al. Dec 2006 A1
20060280227 Pinkney Dec 2006 A1
20060282001 Noel Dec 2006 A1
20060283640 Mercure Dec 2006 A1
20060293607 Alt Dec 2006 A1
20070002038 Suzuki Jan 2007 A1
20070006636 King et al. Jan 2007 A1
20070008113 Spoonhower et al. Jan 2007 A1
20070016089 Fischell et al. Jan 2007 A1
20070027386 Such Feb 2007 A1
20070027388 Chou Feb 2007 A1
20070038054 Zhou Feb 2007 A1
20070049339 Barak et al. Mar 2007 A1
20070055038 Shimizu et al. Mar 2007 A1
20070060737 Ball Mar 2007 A1
20070073353 Rooney et al. Mar 2007 A1
20070096765 Kagan May 2007 A1
20070106346 Bergelson May 2007 A1
20070123772 Euliano May 2007 A1
20070129622 Bourget Jun 2007 A1
20070130287 Kumar Jun 2007 A1
20070135803 Belson Jun 2007 A1
20070142721 Berner et al. Jun 2007 A1
20070156016 Betesh Jul 2007 A1
20070162089 Mosesov Jul 2007 A1
20070162090 Penner Jul 2007 A1
20070164752 Kato Jul 2007 A1
20070167495 Brown et al. Jul 2007 A1
20070167848 Kuo et al. Jul 2007 A1
20070173701 Al-Ali Jul 2007 A1
20070131002 Ge Aug 2007 A1
20070179347 Tarassenko et al. Aug 2007 A1
20070180047 Dong et al. Aug 2007 A1
20070185333 Zhou Aug 2007 A1
20070196456 Stevens Aug 2007 A1
20070207733 Myer Sep 2007 A1
20070213659 Trovato et al. Sep 2007 A1
20070237719 Jones Oct 2007 A1
20070244370 Kuo et al. Oct 2007 A1
20070249946 Kumar et al. Oct 2007 A1
20070255198 Leong et al. Nov 2007 A1
20070255330 Lee Nov 2007 A1
20070270672 Hayter Nov 2007 A1
20070279217 Venkatraman Dec 2007 A1
20070282174 Sabatino Dec 2007 A1
20070282177 Pilz Dec 2007 A1
20070291715 Laroia et al. Dec 2007 A1
20070299480 Hill Dec 2007 A1
20080014866 Lipowshi Jan 2008 A1
20080015421 Penner Jan 2008 A1
20080015494 Santini et al. Jan 2008 A1
20080020037 Robertson et al. Jan 2008 A1
20080021519 DeGeest Jan 2008 A1
20080021521 Shah Jan 2008 A1
20080027679 Shklarski Jan 2008 A1
20080033273 Zhou Feb 2008 A1
20080044025 Corndorf Feb 2008 A1
20080045843 Tsuji et al. Feb 2008 A1
20080046038 Hill Feb 2008 A1
20080051667 Goidreich Feb 2008 A1
20080051767 Rossing et al. Feb 2008 A1
20080058614 Banet Mar 2008 A1
20080062856 Feher Mar 2008 A1
20080065168 Bitton et al. Mar 2008 A1
20080069397 Bartsch Mar 2008 A1
20080074307 Boric-Lubecke Mar 2008 A1
20080077015 Botic-Lubecke Mar 2008 A1
20080077028 Schaldach et al. Mar 2008 A1
20080077188 Denker et al. Mar 2008 A1
20080091089 Guillory et al. Apr 2008 A1
20080091114 Min Apr 2008 A1
20080097549 Colbaugh Apr 2008 A1
20080097917 Dicks Apr 2008 A1
20080099366 Niemic et al. May 2008 A1
20080103440 Ferren et al. May 2008 A1
20080112885 Okunev et al. May 2008 A1
20080114224 Bandy et al. May 2008 A1
20080119705 Patel May 2008 A1
20080119716 Boric-Lubecke May 2008 A1
20080137566 Marholev Jun 2008 A1
20080139907 Rao et al. Jun 2008 A1
20080139953 Baker Jun 2008 A1
20080140403 Hughes et al. Jun 2008 A1
20080146871 Arneson et al. Jun 2008 A1
20080146889 Young Jun 2008 A1
20080146892 LeBeouf Jun 2008 A1
20080154194 Lamego Jun 2008 A1
20080166992 Ricordi Jul 2008 A1
20080183245 Van Oort Jul 2008 A1
20080188837 Belsky et al. Aug 2008 A1
20080194912 Trovato et al. Aug 2008 A1
20080208009 Shklarski Aug 2008 A1
20080212488 Okada et al. Sep 2008 A1
20080214901 Gehman Sep 2008 A1
20080214985 Yanaki Sep 2008 A1
20080243020 Chou Oct 2008 A1
20080249360 Li Oct 2008 A1
20080262320 Schaefer et al. Oct 2008 A1
20080262336 Ryu Oct 2008 A1
20080269664 Trovato et al. Oct 2008 A1
20080275312 Mosesov Nov 2008 A1
20080284599 Zdeblick et al. Nov 2008 A1
20080288026 Cross et al. Nov 2008 A1
20080288027 Kroll Nov 2008 A1
20080294020 Sapounas Nov 2008 A1
20080300572 Rankers Dec 2008 A1
20080303638 Nguyen Dec 2008 A1
20080306357 Korman Dec 2008 A1
20080306359 Zdeblick et al. Dec 2008 A1
20080306360 Robertson et al. Dec 2008 A1
20080306362 Davis Dec 2008 A1
20080311852 Hansen Dec 2008 A1
20080312522 Rowlandson Dec 2008 A1
20080316020 Robertson Dec 2008 A1
20090009332 Nunez et al. Jan 2009 A1
20090018409 Banet Jan 2009 A1
20090024045 Prakash Jan 2009 A1
20090030293 Cooper et al. Jan 2009 A1
20090030297 Miller Jan 2009 A1
20090034209 Joo Feb 2009 A1
20090043171 Rule Feb 2009 A1
20090048498 Riskey Feb 2009 A1
20090062634 Say et al. Mar 2009 A1
20090062670 Sterling Mar 2009 A1
20090062730 Woo Mar 2009 A1
20090069642 Gao Mar 2009 A1
20090069655 Say et al. Mar 2009 A1
20090069656 Say et al. Mar 2009 A1
20090069657 Say et al. Mar 2009 A1
20090069658 Say et al. Mar 2009 A1
20090069724 Otto et al. Mar 2009 A1
20090076343 James Mar 2009 A1
20090076350 Bly et al. Mar 2009 A1
20090076397 Libbus et al. Mar 2009 A1
20090082645 Hafezi et al. Mar 2009 A1
20090088618 Arneson Apr 2009 A1
20090099435 Say et al. Apr 2009 A1
20090110148 Zhang Apr 2009 A1
20090112626 Talbot Apr 2009 A1
20090124871 Arshak May 2009 A1
20090131774 Sweitzer May 2009 A1
20090135886 Robertson et al. May 2009 A1
20090153387 Li et al. Jun 2009 A1
20090157113 Marcotte Jun 2009 A1
20090157358 Kim Jun 2009 A1
20090161602 Matsumoto Jun 2009 A1
20090163789 Say et al. Jun 2009 A1
20090171180 Pering Jul 2009 A1
20090173628 Say et al. Jul 2009 A1
20090177055 Say et al. Jul 2009 A1
20090177056 Say et al. Jul 2009 A1
20090177057 Say et al. Jul 2009 A1
20090177058 Say et al. Jul 2009 A1
20090177059 Say et al. Jul 2009 A1
20090177060 Say et al. Jul 2009 A1
20090177061 Say et al. Jul 2009 A1
20090177062 Say et al. Jul 2009 A1
20090177063 Say et al. Jul 2009 A1
20090177064 Say et al. Jul 2009 A1
20090177065 Say et al. Jul 2009 A1
20090177066 Say et al. Jul 2009 A1
20090182206 Najafi Jul 2009 A1
20090182214 Say et al. Jul 2009 A1
20090182215 Say et al. Jul 2009 A1
20090182388 Von Arx Jul 2009 A1
20090187088 Say et al. Jul 2009 A1
20090187089 Say et al. Jul 2009 A1
20090187090 Say et al. Jul 2009 A1
20090187091 Say et al. Jul 2009 A1
20090187092 Say et al. Jul 2009 A1
20090187093 Say et al. Jul 2009 A1
20090187094 Say et al. Jul 2009 A1
20090187095 Say et al. Jul 2009 A1
20090187381 King et al. Jul 2009 A1
20090192351 Nishino Jul 2009 A1
20090192368 Say et al. Jul 2009 A1
20090192369 Say et al. Jul 2009 A1
20090192370 Say et al. Jul 2009 A1
20090192371 Say et al. Jul 2009 A1
20090192372 Say et al. Jul 2009 A1
20090192373 Say et al. Jul 2009 A1
20090192374 Say et al. Jul 2009 A1
20090192375 Say et al. Jul 2009 A1
20090192376 Say et al. Jul 2009 A1
20090192377 Say et al. Jul 2009 A1
20090192378 Say et al. Jul 2009 A1
20090192379 Say et al. Jul 2009 A1
20090198115 Say et al. Aug 2009 A1
20090198116 Say et al. Aug 2009 A1
20090198175 Say et al. Aug 2009 A1
20090199282 Tsitkova et al. Aug 2009 A1
20090203964 Shimizu et al. Aug 2009 A1
20090203971 Sciarappa Aug 2009 A1
20090203972 Heneghan Aug 2009 A1
20090203978 Say et al. Aug 2009 A1
20090204265 Hackett Aug 2009 A1
20090210164 Say et al. Aug 2009 A1
20090216101 Say et al. Aug 2009 A1
20090216102 Say et al. Aug 2009 A1
20090226214 Say et al. Sep 2009 A1
20090227204 Robertson et al. Sep 2009 A1
20090227876 Tran Sep 2009 A1
20090227940 Say et al. Sep 2009 A1
20090227941 Say et al. Sep 2009 A1
20090231125 Baldus Sep 2009 A1
20090234200 Husheer Sep 2009 A1
20090243833 Huang Oct 2009 A1
20090253360 Takenaka et al. Oct 2009 A1
20090256702 Robertson Oct 2009 A1
20090258669 Nie et al. Oct 2009 A1
20090264714 Chou Oct 2009 A1
20090264964 Abrahamson Oct 2009 A1
20090265186 Tarassenko et al. Oct 2009 A1
20090273467 Elixmann Nov 2009 A1
20090281539 Selig Nov 2009 A1
20090287109 Ferren et al. Nov 2009 A1
20090292194 Libbus et al. Nov 2009 A1
20090295548 Ronkka Dec 2009 A1
20090296677 Mahany Dec 2009 A1
20090301925 Alloro et al. Dec 2009 A1
20090303920 Mahany Dec 2009 A1
20090309708 Hasegawa Dec 2009 A1
20090312619 Say et al. Dec 2009 A1
20090318761 Rabinovitz Dec 2009 A1
20090318779 Tran Dec 2009 A1
20090318783 Rohde Dec 2009 A1
20090318793 Datta Dec 2009 A1
20100010330 Rankers Jan 2010 A1
20100033324 Shimizu et al. Feb 2010 A1
20100036263 Ferren et al. Feb 2010 A1
20100049006 Magar Feb 2010 A1
20100049012 Dijksman et al. Feb 2010 A1
20100049069 Tarassenko et al. Feb 2010 A1
20100049263 Reeve Feb 2010 A1
20100056878 Partin Mar 2010 A1
20100056891 Say et al. Mar 2010 A1
20100056939 Tarassenko et al. Mar 2010 A1
20100057041 Hayter Mar 2010 A1
20100060300 Muller Mar 2010 A1
20100062709 Kato Mar 2010 A1
20100063438 Bengtsson Mar 2010 A1
20100063841 D'Ambrosia et al. Mar 2010 A1
20100069002 Rong Mar 2010 A1
20100069717 Hafezi et al. Mar 2010 A1
20100099369 Say et al. Apr 2010 A1
20100099967 Say et al. Apr 2010 A1
20100099968 Say et al. Apr 2010 A1
20100100077 Rush Apr 2010 A1
20100100078 Say et al. Apr 2010 A1
20100106001 Say et al. Apr 2010 A1
20100113950 Lin May 2010 A1
20100118853 Godfrey May 2010 A1
20100121315 Trovato et al. May 2010 A1
20100128175 Lin May 2010 A1
20100139672 Kroll et al. Jun 2010 A1
20100160742 Seidl et al. Jun 2010 A1
20100168659 Say et al. Jul 2010 A1
20100179398 Say et al. Jul 2010 A1
20100185055 Robertson Jul 2010 A1
20100191073 Tarassenko et al. Jul 2010 A1
20100210299 Gorbachov Aug 2010 A1
20100218249 Wilson et al. Aug 2010 A1
20100222652 Cho Sep 2010 A1
20100228113 Solosko Sep 2010 A1
20100234706 Gilland Sep 2010 A1
20100234715 Shin Sep 2010 A1
20100234914 Shen Sep 2010 A1
20100245091 Singh Sep 2010 A1
20100249541 Geva et al. Sep 2010 A1
20100249881 Corndorf Sep 2010 A1
20100256461 Mohamedali Oct 2010 A1
20100259543 Tarassenko et al. Oct 2010 A1
20100268048 Say et al. Oct 2010 A1
20100268049 Say et al. Oct 2010 A1
20100268050 Say et al. Oct 2010 A1
20100274111 Say et al. Oct 2010 A1
20100280345 Say et al. Nov 2010 A1
20100280346 Say et al. Nov 2010 A1
20100298650 Moon et al. Nov 2010 A1
20100298730 Tarassenko et al. Nov 2010 A1
20100311482 Lange Dec 2010 A1
20100312580 Tarassenko et al. Dec 2010 A1
20110004079 Al Ali et al. Jan 2011 A1
20110065983 Hafezi et al. Mar 2011 A1
20110081860 Brown et al. Apr 2011 A1
20110124983 Kroll et al. May 2011 A1
20110134906 Garudadri et al. Jun 2011 A1
20110160549 Saroka et al. Jun 2011 A1
20110166937 Bangera et al. Jul 2011 A1
20110144470 Mazar et al. Aug 2011 A1
20110196454 Strand et al. Aug 2011 A1
20110208013 Phan et al. Aug 2011 A1
20110237922 Parker, III Sep 2011 A1
20110237924 McGusty et al. Sep 2011 A1
20110270135 Dooley et al. Nov 2011 A1
20110279963 Kumar et al. Nov 2011 A1
20120016231 Westmoreland Jan 2012 A1
20120029307 Paquet et al. Feb 2012 A1
20120029309 Paquet et al. Feb 2012 A1
20120032816 Cho et al. Feb 2012 A1
20120071743 Todorov et al. Mar 2012 A1
20120083715 Yuen et al. Apr 2012 A1
20120086550 LeBlanc et al. Apr 2012 A1
20120089000 Bishay et al. Apr 2012 A1
20120101396 Solosko et al. Apr 2012 A1
20120163426 Nemeth Jun 2012 A1
20120179004 Roesic et al. Jul 2012 A1
20120197144 Christ et al. Aug 2012 A1
20120299723 Hafezi et al. Nov 2012 A1
20120306662 Vosch Dec 2012 A1
20120310070 Kumar et al. Dec 2012 A1
20120316413 Liu et al. Dec 2012 A1
20120323136 Shiftman et al. Dec 2012 A1
20130002435 Utter, II Jan 2013 A1
20130006009 Raichle et al. Jan 2013 A1
20130021166 Shah Jan 2013 A1
20130027344 Choon Jan 2013 A1
20130030259 Thomsen et al. Jan 2013 A1
20130057385 Murakami et al. Mar 2013 A1
20130060115 Gehman et al. Mar 2013 A1
20130171596 French Jul 2013 A1
20130185228 Dresner Jul 2013 A1
20130194118 Coln et al. Aug 2013 A1
20130196012 Dill Aug 2013 A1
20130218022 Larsen et al. Aug 2013 A1
20130231188 Berberich et al. Sep 2013 A1
20130238647 Thompson Sep 2013 A1
20130275296 Tietzen et al. Oct 2013 A1
20140051946 Arne et al. Feb 2014 A1
20140066726 Costello Mar 2014 A1
20140280125 Bhatdwaj et al. Sep 2014 A1
20140300490 Kotz Oct 2014 A1
20140308930 Tran Oct 2014 A1
20140349256 Connor Nov 2014 A1
20140374276 Guthrie et al. Dec 2014 A1
20150080678 Frank et al. Mar 2015 A1
20150080679 Frank et al. Mar 2015 A1
20150080680 Zdeblick et al. Mar 2015 A1
20150080681 Hafezi et al. Mar 2015 A1
20150127737 Thompson et al. May 2015 A1
20150127738 Thompson et al. May 2015 A1
20150149375 Thompson et al. May 2015 A1
20150182170 Zdeblick et al. Jul 2015 A1
20150248833 Arne et al. Sep 2015 A1
20160324442 Zdeblick et al. Nov 2016 A1
20180184698 Arne et al. Jul 2018 A1
20190191006 Thompson Jun 2019 A1
20190261888 Zdeblick et al. Aug 2019 A1
Foreign Referenced Citations (188)
Number Date Country
1588649 Mar 2005 CN
1991868 Jul 2007 CN
101005470 Jul 2007 CN
101032396 Sep 2007 CN
201076456 Jun 2008 CN
10313005 Oct 2004 DE
0526166 Feb 1993 EP
1246356 Oct 2002 EP
1451595 Sep 2004 EP
1530224 May 2005 EP
1789128 May 2007 EP
2063535 May 2009 EP
2143369 Jan 2010 EP
61072712 Apr 1986 JP
S62112529 May 1987 JP
05228128 Sep 1993 JP
1014898 Jan 1998 JP
H11195415 Jul 1999 JP
2000506410 May 2000 JP
2001070267 Mar 2001 JP
2001198096 Jul 2001 JP
2002224053 Aug 2002 JP
2002282219 Oct 2002 JP
2002291684 Oct 2002 JP
2003050867 Feb 2003 JP
2004007187 Jan 2004 JP
2004313242 Nov 2004 JP
2005073886 Mar 2005 JP
2005102959 Apr 2005 JP
2005137683 Jun 2005 JP
2005304880 Nov 2005 JP
2005532841 Nov 2005 JP
2005532849 Nov 2005 JP
2006508752 Mar 2006 JP
2006509574 Mar 2006 JP
2006136405 Jun 2006 JP
2006177699 Jul 2006 JP
2008212488 Sep 2006 JP
2006268614 Oct 2006 JP
2007167448 Jul 2007 JP
2007200739 Aug 2007 JP
2007313340 Dec 2007 JP
2008011865 Jan 2008 JP
2008501415 Jan 2008 JP
2008086390 Apr 2008 JP
2008181295 Aug 2008 JP
2008191110 Aug 2008 JP
2009528909 Aug 2009 JP
2010049490 Mar 2010 JP
2010-511465 Apr 2010 JP
2011086027 Apr 2011 JP
2012039370 Feb 2012 JP
2012200309 Oct 2012 JP
2012212362 Nov 2012 JP
2016-517317 Jun 2016 JP
927471 Nov 2009 KR
10-2012-093995 Mar 2012 KR
553735 Mar 2003 TW
200724094 Jul 2007 TW
WO1988002237 Apr 1988 WO
WO1993008734 May 1993 WO
WO1993019667 Oct 1993 WO
WO1997014112 Apr 1997 WO
WO1998043537 Oct 1998 WO
WO1999059465 Nov 1999 WO
WO2000033246 Jun 2000 WO
2000062667 Oct 2000 WO
0062667 Oct 2000 WO
WO2001000085 Jan 2001 WO
WO2001047466 Jul 2001 WO
WO2001074011 Oct 2001 WO
WO2001080731 Nov 2001 WO
WO2002045489 Jun 2002 WO
WO2002058330 Jul 2002 WO
WO2002062276 Aug 2002 WO
WO2002087681 Nov 2002 WO
WO2003050643 Jun 2003 WO
2003056491 Jul 2003 WO
WO2004014225 Feb 2004 WO
WO2004075751 Mar 2004 WO
WO2004039256 May 2004 WO
WO2004059551 Jul 2004 WO
WO2004066834 Aug 2004 WO
WO2004068748 Aug 2004 WO
WO2004068881 Aug 2004 WO
WO2004109316 Dec 2004 WO
WO2005011237 Feb 2005 WO
WO2005013503 Feb 2005 WO
WO2005020023 Mar 2005 WO
WO2005024687 Mar 2005 WO
WO2005084533 Mar 2005 WO
WO2005041767 May 2005 WO
WO2005046575 May 2005 WO
WO2005047837 May 2005 WO
WO2005051166 Jun 2005 WO
WO2005055448 Jun 2005 WO
WO2005082436 Sep 2005 WO
WO2005110238 Nov 2005 WO
WO2006027586 Mar 2006 WO
WO2006035351 Apr 2006 WO
WO2006046648 May 2006 WO
WO2006055892 May 2006 WO
WO2006055956 May 2006 WO
WO2006066566 Jun 2006 WO
WO2006075016 Jul 2006 WO
WO2006094513 Sep 2006 WO
WO2006100620 Sep 2006 WO
WO2006104843 Oct 2006 WO
WO2006109072 Oct 2006 WO
WO2006116718 Nov 2006 WO
WO2006119345 Nov 2006 WO
WO2006127355 Nov 2006 WO
WO2007001724 Jan 2007 WO
WO2007001742 Jan 2007 WO
WO2007013952 Feb 2007 WO
WO2007014084 Feb 2007 WO
WO2007014527 Feb 2007 WO
WO2007021496 Feb 2007 WO
WO2007027660 Mar 2007 WO
WO2007028035 Mar 2007 WO
WO2007036687 Apr 2007 WO
WO2007036741 Apr 2007 WO
WO2007036746 Apr 2007 WO
WO2007040878 Apr 2007 WO
WO2007071180 Jun 2007 WO
WO2007096810 Aug 2007 WO
WO2007101141 Sep 2007 WO
WO2007120946 Oct 2007 WO
WO2007127316 Nov 2007 WO
WO2007127455 Nov 2007 WO
WO2007127879 Nov 2007 WO
WO2007128165 Nov 2007 WO
WO2007130491 Nov 2007 WO
WO2007143535 Dec 2007 WO
WO2007149546 Dec 2007 WO
WO2008002239 Jan 2008 WO
WO2008008281 Jan 2008 WO
WO2008030482 Mar 2008 WO
WO2008052136 May 2008 WO
WO2008063626 May 2008 WO
2008068695 Jun 2008 WO
WO2008066617 Jun 2008 WO
WO2008068695 Jun 2008 WO
WO2008076464 Jun 2008 WO
WO2008089232 Jul 2008 WO
WO2008091683 Jul 2008 WO
WO2008095183 Aug 2008 WO
WO2008097652 Aug 2008 WO
WO2008101107 Aug 2008 WO
WO2008112577 Sep 2008 WO
WO2008112578 Sep 2008 WO
WO2008120156 Oct 2008 WO
WO2008133394 Nov 2008 WO
WO2008134185 Nov 2008 WO
WO2008150633 Dec 2008 WO
WO2009001108 Dec 2008 WO
WO2009006615 Jan 2009 WO
WO2009029453 Mar 2009 WO
WO2009031149 Mar 2009 WO
WO2009035773 Mar 2009 WO
WO2009036334 Mar 2009 WO
WO2009051829 Apr 2009 WO
WO2009051830 Apr 2009 WO
WO2009063377 May 2009 WO
WO2009081348 Jul 2009 WO
WO2009111664 Sep 2009 WO
WO2009146082 Dec 2009 WO
WO2010003175 Jan 2010 WO
WO2010009100 Jan 2010 WO
WO2010011833 Jan 2010 WO
WO2010019778 Feb 2010 WO
WO2010105053 Mar 2010 WO
WO2010057049 May 2010 WO
WO2010075115 Jul 2010 WO
WO2010080843 Jul 2010 WO
WO2010107563 Sep 2010 WO
WO2010115194 Oct 2010 WO
WO2010132331 Nov 2010 WO
WO2010135516 Nov 2010 WO
WO2012104657 Aug 2012 WO
WO2012112561 Aug 2012 WO
2012125425 Sep 2012 WO
WO2012158190 Nov 2012 WO
WO2013012869 Jan 2013 WO
2014151925 Sep 2014 WO
WO2015042411 Mar 2015 WO
WO2015044722 Apr 2015 WO
WO2015112603 Jul 2015 WO
Non-Patent Literature Citations (69)
Entry
Kang et al., “Nonwoven Fabric Active Elechudes for Biopotential Measurement During Normal Daily Activity,” IEEE Trans Biomed Eng. Jan. 2008: vol. 55, No. 1, pp. 188-195.
AADE, “AADE 37th Annual Meeting San Antonio Aug. 4-7, 2010” American Association of Diabetes Educators (2010); http://www.diabeteseducator.org/annualmeeting/2010/index.html; 2 pp.
Arshak et al., A Review and Adaptation of Methods of Object Tracking to Telemetry Capsules IC-Med (2007) vol. 1, No. 1, Issue 1, 12 pp.
“ASGE Technology Status Evaluation Report: wireless capsule endoscopy” American Soc. for Gastrointestinal Endoscopy (2006) vol. 63, No. 4; 7 pp.
Au-Yeung, K., et ai., “A Networked System for Seif-Management of Drug Therapy and Wellness”, Wireless Health '10, Oct. 5-7, 2010, San Diego, 9 pages.
Aydin et al., “Design and implementation considerations for an advanced wireless interface in miniaturized integrated sensor Microsystems” Sch. of Eng. & Electron., Edinburgh Univ., UK; (2003); abstract.
BARRIE. Heidelberg pH capsule gastric analysis Texbook of Natural Medicine, (1992), Pizzomo, Murray & Barrie.
Baskiyar, S. “A Real-time Fault Tolerant Intra-body Network” Dept. of Comp. Sci & Soft Eng; Auburn University; Proceedings ofthe 27th Annual IEEE Conference; 0742-1303/02 (2002) IEEE; 6 pp.
Bergogne C., et at, “A new freguency estimator applied to burst transmission”, IEEE International Conference on Acoustics, Speech and Signal Processing, Apr. 21, 1997, vol. 1, pp. 267-270.
Brock, “Smart Medicine: The Application of Auto-ID Technology to Healthcare” Auto-ID Labs (2002) http://www.autoidlabs.org/uploads/media/MIT-AUTOID-WH-010.pdf.
Carlson et al., “Evaluation of a non-invasive respiratory monitoring system for sleeping subjects” Physiological Measurement (1999) 20(1): 53.
Delvaux et al., “Capsule endoscopy: Technique and indications” Clinical Gastoenterology (2008) vol. 22, Issue 5, pp. 813-837.
Description of ePatch Technology Platform for ECG and EMG, located it http://www.madebydelta.com/imported/images/DELTA_Web/documents/ME/ePatch_ECG_EMG.pdf, Dated Sep. 2, 2010.
Evanczuk, S., “PIC MCU software library uses human body for secure communications link” EDN Network; edn.com; Feb. 26 (2013) Retrieved from internet Jun. 19, 2013 at http://www.edn.com/electronics-products/other/4407842/PIC-MCU-software-library-uses-human-body-for-secure-communications-link; 5 pp.
Fawaz et al., “Enhanced Telemetry System using CP-QPSK Band-Pass Modulation Technique Suitable for Smart Pill Medical Application” IFIP IEEE Dubai Conference (2008); http://www.asic.fh-offenburg.de/downloads/ePille/IFIP_IEEE_Dubai_Conference.pdf.
Gilson, D.R. “Molecular dynamics simulation of dipole interactions”, Department of Physics, Hull University, Dec. (2002), p. 1-43.
Given Imaging, “Agile Patency Brochure” (2006) http://www.inclino.no/documents/AgilePatencyBrochure_Giobal_GMB-0118-01.pdf; 4pp.
Gonzalez-Guillaumin et al., “Ingestible capsule for impedance and pH monitoring in the esophagus”IEEE Trans Biomed Eng. (2007) 54(12: 2231-6; abstract.
Greene, “Edible RFID microchip monitor can tell if you take your medicine” Bloomberg Businessweek (2010) 2 pp.; http://www.businessweek.com/idg/2010-03-31/edible-rfid-microchip-monitor-can-tell-if-you-take-your-medicine.html.
Halthion Medical Technologies “Providing Ambulatory Medical Devices Which Monitor, Measure and Record” webpage. Online website: http://www.halthion.com/; downloaded May 30, 2012.
Heydari et al., “Analysis ofthe PLL jitter due to power/ground and substrate noise”; IEEE Transactions Circuits and Systems (2804) 51(12): 2404-16.
Hoover et al., “Rx for health: Engineers design pill that signals it has been swallowed” University of Florida News (2810) 2pp.; http://news.ufi.edu/2010/03/31/antenna-pill-2/.
Hotz “The Really Smart Phone” The Wall Street Journal. What They Know (2011); 6 pp.: http://online.wsj.com/article/SB10001424052748704547604576263261679848814.html?mod=djemTECH_t.
Intromedic, MicroCam Innovative Capsule Endoscope Pamphlet. (2006) 8 pp (http://www.intromedic.com/en/product/productinfo.asp).
ISFET—Ion Sensitive Field-Effect Transistor; Microsens S.A. pdf document. First cited by Examiner in Office Action dated Jun. 13, 2011 for U.S. Appl. No. 12/238,345; 4pp.
Jung, S. “Dissolvable ‘Transient Electronics’ Will Be Good for Your Body and the Environment” MedGadget; Oct. 1, 2012; Onlne website: http://medgadget.com/2012/10/dissolvable-transient-electronics-will-be-good-for-your-body-and-the-environment.html; downloaded Oct. 24, 2012: 4 pp.
Juvenile Diabetes Research Foundation International (JDRF), “Artificial Pancreas Project” (2010); http://www.artlficialpancreasproject.com/; 3 pp.
Li, P-Y, et al. “An electrochemical intraocular drug delivery device”, Sensors and Actuators A 143 (2008) pp. 41-48.
Lifescan, “OneTouch UltraLink™” http://www.lifescan.com/products/meters/ultralink (2010) 2 pp.
Mackay et al., “Radio Telemetering from within the Body Inside Information is Revealed by Tiny ransmitters that can be Swallowed or Implanted in Man or Animal” Science (1991) 1196-1202; 134; American Association for the Advancement of Science, Washington D.C.
Mackay et al., “Endoradiosonde” Nature, (1957) 1239-1240, 179 Nature Publishing Group.
McKenzie et al., “Validation of a new telemetric core temperature monitor” J. Therm. Biol. (2004) 29(7-8):605-11.
Medtronic, “CareLink Therapy Management Software for Diabetes” (2010); https://carelink.minimed.com/patient/entry.jsp?bhcp=1; 1 pp.
Medtronic, “Carelink™ USB” (2008) http://www.medtronicdiabetes.com/pdf/carelink_usb_factsheet.pdf 2pp.
Medtronic “The New MiniMed Paradigm® REAL-Time Revel™ System” (2010) http://www.medtronicdiabetes.com/products/index.html; 2 pp.
Medtronic, “MINI MED Paradigm ® Revel ™ Insulin Pump” (2010) http://www.medtronicdiabetes.com/products/insulinpumps/index.html; 2 pp.
Medtronic, Mini Med Paradigm™ Veo™ System: Factsheet (2010). http://www.medtronic-diabetes.com.au/downloads/Paradigm%20Veo%20Factsheet.pdf ; 4 pp.
Melanson, “Walkers swallow RFID pills for science” Engadget (2008); http://www.engadget.com/2008/07/29/walkers-swallow-rfid-pills-for-science/.
Minimitter Co. Inc. “Actiheart” Traditional 510(k) Summary Sep. 27, 2005.
Minimitter Co. Inc. Noninvasive technology to help your studies succeed. Mini Mitter.com Mar. 31, 2009.
Mini Mitter Go, Inc. 510(k) Premarket Notification Mini-Logger for Diagnostic Spirometer 9-21 (1999).
Mini Mitter Co, Inc. 510(k) Premarket Notification for VitalSense. Apr. 22, 2004.
Minimitter Go. Inc. VitalSense Integrated Physiological Monitoring System. Product Description. (2005).
Minimitter Co. Inc. VitalSense Wireless Vital Signs Monitoring. Temperatures.com Mar. 31, 2009.
Mojaverian et al., “Estimation of gastric residence time of the Heidelberg capsule in humans: effect of varying food composition” Gastroenterology (1985) 89:(2): 392-7.
“New ‘smart pill’ to track adherence” E-Health-insider (2010) http://www.e-health-insider.com/news/5910/new_‘smart_pill’_monitors_medicines.
Owano, N., “Study proposes smart sutures with sensors for wounds” phys.org. Aug. 2012. http://phys.org/news/2012-08-smart-sutures-sensors-wounds.html.
Park, “Medtronic to Buy MiniMed for 33.7 Billion” (2001) HomeCare; http://homecaremag.com/mag/medical_medtronic_buy_minimed/; 2 pp.
Radio Antennae, http://www.erikdeman.de/html/sail018h.htm; (2008) 5 pages.
“RFID “pill” monitors marchers” RFID News (2008) http://www.rfidnews.org/2008/07/23/rfid-pill-monitors-marchers/.
Sanduleanu et ai., “Octave tunable, highly linear, RC-rina oscillator with differential fine-coarse tuning. quadrature outputs and amplitude control for fiber optic transceivers” (2002) IEEE MTT-S International Microwave Symposium Digest 545-8.
Santini, J.T. et al, “Microchips as controlled drug delivery-devices”, Agnew. Chem. Int. Ed. (2800), vol. 39, pp. 2396-2407.
“SensiVida minimally invasive clinical systems” Investor Presentation October (2009) 28pp; http://www.sensividamedtech.com/SensiVidaGeneralOctober09.pdf.
Shawgo. R.S. et al. “BioMEMS from drug delivery”, Current Opinion in Solid State and Material Science 6 (2802), p. 329-334.
Shrivas et al., “A New Platform for Bioelectronics-Electronic Pill”, Cummins College, (2010).; http://www.cumminscollege.org/downloads/electronios_and_telecommunication/Newsletters/Current%20Newsletters.pdf; First cited in third party client search conducted by Patent Eagle Search May 18, 2010 (2010).
“Smartlife awarded patent for knitted transducer” Innovation in Textiles News: http://www.innovationintextiles.com/articles/206.php: 2pp. (2009).
“The SmartPill Wireless Motility Capsule” SMARTPILL, The Measure of GI Health; (2010) hitp://www.smartpillcorp.com/index.cfm?pagepath=Products/The_SmartPill_Capsule&id-17814.
Solanas et al., “RFID Technology for the Health Care Sector” Recent Patents on Electrical Engineering (2008) 1, 22-31.
Soper, S.A. et al. “Bio-Mems Technologies and Applications”, Chapter 12, “MEMS for Drug Delivery”, p. 325-346 (2007).
Swedberg, “University Team Sees Ingestible RFID Tag as a Boon to Clinical Trials” RFID Journal April 27, 2010; http://www.rfidjournal.com/article/view/7560/1.
Tajalli et al., “Improving the power-delay performance in subthreshold source-coupled logic circuits” Integrated Circuit and System Design. Power and Timing Modeling, Optimization and Simulation, Springer Berlin Heidelberg (2008) 21-30.
Tatbul et al., “Confidence-based data management for personal area sensor networks” ACM International Conference Proceeding Series (2004) 72.
Tierney, M.J. et al. “Electroreleasing Composite Membranes for Delivery of Insulin and other Biomacromolecules”, J. Electrochem. Soc., vol. 137, No. 6, Jun. 1990, p. 2005-2006.
Walkey, “MOSFET Structure and Processing”: 97.398* Physical Electronics Lecture 20, 24 pages, First cited by Examiner in Office Action dated Jun. 13, 2011 for U.S. Appl. No. 12/238,345.
Xiaoming et al., “A telemedicine system for wireless home healthcare based on bluetooth and the internet” Telemedicine Journal and e-health (2004) 10(S2): S110-6.
Yang et al., “Fast-switching frequency synthesizer with a discriminator-aided phase detector” IEEE Journal of Solid-State Circuits (2000) 35(10): 1445-52.
Yao et al., “Low Power Digttal Communication in implantable Devices Using Volume Conduction of Biological Tissues” Proceedings of the 28th IEEE, EMBS Annual International Conference, Aug. 30-Sep. 3, 2006.
Zimmerman, “Personal Area Networks: Near-field intrabody communication” IBM Systems Journal (1996) 35 (3-4):609-17.
Zworykin, “A Radio Pill” Nature, (1957) 898, 179 Nature Publishing Group.
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