Disclosed herein are systems and methods for producing and using electrodes, which may be flexible and/or stretchable, and interconnection structures that can be used both externally and/or implanted within the body. Electrodes according to various embodiments disclosed herein may be produced by depositing patterned layers of insulating and conductive polymers to form multi-layer circuits. The conductive materials and layers in the structure can be exposed on the surface of the structures for use as electrodes. A plurality of electrodes may be formed into an electrode array. In various embodiments, electrode arrays may be associated with telemetry modules configured to wirelessly exchange data between an implantable component and an external module.
Certain embodiments may be suited for short-term implantation, while other embodiments may be suited for long-term implantation. Still other embodiments may be used for in vitro applications. Some applications of the systems and methods disclosed herein may include recording from and stimulation of neural tissue, stimulation of muscles, sub- and epi-dural monitoring, use in connection with a blink prosthesis, use in treating incontinence via posterior tibial nerve stimulation, use in restoring sexual function via stimulation of the spinal cord, use in recording implanted EMG and neural signals for use in prosthesis control, use in the stimulation of the recurrent laryngeal nerve for treatment of dystonia, use in stimulation of peripheral nerves for nerve block, and use in connection with neuroprosthetic and neural interface applications (e.g., a pacemaker device).
Multiple types of conductive polymers can be used within the same structure depending on factors, such as cost, conductivity, biocompatibility, and manufacturability for different feature sizes. For example, exposed electrode areas can also be formed from a conductive polymer that is different from conductive polymers used within the structures.
According to various embodiments, electrodes on the surface of the structure can also be formed by embedding metal or other electrode materials into the structures, and connecting to them with conductive polymers. These electrodes may also include geometrical and structural features for penetrating into tissues, hooking or providing mechanical fixation, mitigating stress around flexion points, or increasing the surface area of the electrode. In some embodiments, conducting traces can also be brought to the surface of the structure to create contact pads for bonding to other devices, including sensors, actuators, or other devices or assemblies. Bonding can be performed by applying pressure to hold the conductive areas in contact with bond pads on the devices, or by applying conductive adhesives or joining materials. These joints can also be further encapsulated with insulating polymers, such as silicones to seal and/or structurally reinforce them.
In various embodiments, electrodes may include embedded electronics. Such electronics may include, but are not limited to, any combination of silicon integrated circuits (“ICs”), circuit boards with electronic components, hermetic enclosures with contacts and feed-throughs to internal electronics, and the like. These electronics may include amplifiers, filters, analog to digital conversion, digital signal processing, stimulators, control circuits, fail-safe monitoring, data error checking, batteries, and connections for data and power telemetry with external devices.
Flexible electrodes, according to the present disclosure, may be manufactured by any method for controlled dispensing and/or forming of insulating and conductive polymers into patterns, including: spraying polymer layers onto a surface; depositing polymer layers through needles and narrow dispensing nozzles, including those that use gas pressure and positive displacement for flow control; depositing polymer layers through an ink jet dispenser (such as picodot systems); depositing polymer layers by screen printing and printing through masks; using optical, plasma, or chemical methods to selectively activate areas of a substrate to facilitate selective coating of areas with patterns of polymers; using laser ablation, or plasma or chemical etching (including use of photolithography or overlay masks) to selectively remove and form patterns in layers of deposited polymers; and depositing polymer layers onto both 2D surfaces and 3D molds.
Applications for electrodes, as disclosed herein, may include any application for which electrodes are currently utilized. Certain embodiments may be employed for sensing of electrophysiological signals from cells, tissues, organs, and body parts, including signals from nerves and muscles, EEG, EMG, ECG, EOG, ERG, ENG, ECoG, EGG, LFP, single and multiunit action potentials, and evoked potentials. Sensing and recording can be performed at the cell, tissue, organ, and body part scales, and used for diagnostic purposes, construction of neuroprosthetic systems for functional restoration, and brain machine interfaces to control external devices based on neural and/or muscle signals. These devices can be used for implanted and external body surface applications, as well as for temporary insertion into and/or application to tissues and organs during surgery and diagnostic procedures, for both short- and long-term sensing purposes.
In addition, various embodiments disclosed herein may be utilized for electrical stimulation of cells, tissues, organs, and body parts, including stimulation of nerves and muscles, for diagnostic purposes, enhancing trophic effects, functional restoration or rehabilitation in Functional Electrical Stimulation (FES) and other neuroprosthesis systems, and neuromodulation applications including Deep Brain Stimulation (DBS) targets, the cerebral cortex, sympathetic and parasympathetic nerves, peripheral nerves, and the spinal cord. These devices can be used for implanted and external body surface applications, as well as for temporary insertion into and/or application to tissues and organs during surgery and diagnostic procedures, for both short- and long-term stimulation purposes.
Still other embodiments may be utilized for sensing potentials and currents related to chemical reactions associated with the electrodes, including reactions for oxygen sensing, pH sensing, protein-specific binding of materials to the electrodes, and other chemical sensors based on electrodes. These may also include chemical modification and/or coating of the electrodes, or use of the electrodes with other application-specific materials necessary to sense these reactions.
Flexible electrodes, as disclosed herein, may be also utilized for control or forcing chemical reactions associated with the electrodes, including release of chemicals or drugs, modification of the local chemical environment, and forcing of chemical reactions. These may also include chemical modification and/or coating of the electrodes, or use of the electrodes with other application-specific materials necessary to create or control these reactions. Various embodiments may also be utilized to control chemical reactions, such as gas evolution or pH changes to effect structural changes in materials, including inflation of balloons and changing the shape, rigidity and forces within the device.
Various embodiments disclosed herein may be utilized to generate and sense electrical currents in the body for device operation, implant integrity, and diagnostic and therapeutic use, including imaging and facilitation of trophic effects and promoting recovery and healing of tissues in the body, including nerves or bone, and restoring function to paralytic and paretic body parts. Measurements of electrode and biological material impedances may be collected, including fixed frequency impedance and multi-frequency impedance spectroscopy methods to characterize electrode interfaces and characteristics of cells, tissues, organs, and body parts of humans and animals, including nerve, muscle and dental tissues. Such measurements may include frequency, phase, and all other measures used to characterize impedances.
Still other uses of flexible electrodes, as disclosed herein, may include measurements of biological material impedances, which may used to compute impedance tomography images at the cell, tissue, organ, and body scale; application of potentials for electrophoresis, microelectrode array dish, and other in vitro applications; application of potentials for electroporation and other electrical modifications of tissues; and creation of voltage gradients to accelerate the delivery or migration of drugs.
Various techniques may be utilized in order to facilitate bonding and/or integration of a flexible electrode into a body. For example, adhesives may be applied to the structures to bond them to the body; coatings, such as hydrogels, PEG structures, or other biomaterials, may be used to modulate the tissue response to the structure, including coatings that release drugs for this purpose; coatings may be applied to the electrode to change the adhesion of body tissues to the structures; drugs may be embedded within the non-conducting or insulating material that are released over time to affect the biocompatibility and local tissue response to the implanted structures; chemical surface modification (e.g., hydrophobic, hydrophilic, or non-stick materials) may be utilized to affect the interaction of the surfaces with materials in the environment or biocompatibility in the body; nanomaterials or coatings (e.g., iridium, conductive polymers, or carbon nano-tubes) may be applied to electrodes to affect their biocompatibility and impedance; radio-opaque alignment markings, identification information, and/or serial numbers may be embedded into the structures for visualization under x-ray; shapes such as protuberances, pits, holes, or other features may be used to increase the surface area of the electrodes; barbs or hooking features may be included to fix the device within the body; flat tabs, strings, loops or other features may be used to grip, glue, and/or suture the electrode for fixation within the body; or a fabric mesh (such as Dacron) may be used for suturing and/or forming strong tissue adhesions to portions of the structure;
Flexible electrodes disclosed herein may be implanted into the body with a variety of methods, including: insertion into epidural and subdural spaces through openings in the cranium; folding/unfolding and/or rolling/unrolling to deploy the structure once inside the body; use of saline and/or air balloons within the structure to affect mechanical changes inside the body for fixation, application of pressure, guidance, manipulation of placement, or other purpose; use of guide needles and other surgical instruments to create pilot holes and channels for insertion of the structures into the tissue; and use of needles or other surgical instruments to push or pull the structures into the tissue, then removing the instruments while leaving the structures in place.
According to various embodiments, insulated conductors may be disposed within a flexible electrode. Providing insulated conductors within the flexible electrode may also allow for the connection of embedded electrodes; the connection of probes and sensors (e.g., accelerometers, pressure sensors, optical and IR sensors, contact switches, magnetic field sensors, capacitive sensors, inductive coils, thermal flux sensors, temperature sensors, proximity sensors, piezo sensors, ultrasound transducers, sound sensors, etc.); the connection of actuators or devices (e.g., force generators, motors, piezo actuators, electromagnets, coils, inductors, ultrasound transducers, stimulators, light emitting diodes etc.); the formation of flexible elastic resistor and capacitor elements that can stretch around tissues and detect structural changes in the sensor by changes in electrical impedance in the sensor elements; the formation of capacitive shields and guard traces for protection of other traces within the structure from interference and electrostatic discharge (ESD); and the measurement of conductivity within the electrode and electrode structures to diagnose problems within the device structure.
Insulating polymer 106 may comprise any flexible and/or elastomeric material that provides electrical insulation. According to various embodiments, insulating polymer 106 may comprise any combination of silicones, siloxanes, polydimethylsiloxane (PDMS), rubber materials, latex materials, polyesters, polypropylenes, polytetrafluoroethylenes (PTFE), Parylenes, liquid crystal polymers, polyimides, polyesterimides, polyamides, polybutyldienes (PBD), flexible copolymers, or any other polymer used for medical applications.
Internal conductive polymer trace 104 may comprise polymers that are intrinsically conductive (including polypyrrole, polyacetylene, polyaniline or poly[dioctyl-bithiophene] (PDOT)), or polymers that are doped with conductive particles. Any type of conductive particle may be utilized in connection with internal conductive polymer trace 104, including any combination of: conductive forms of carbon (including graphite, carbon black, vitreous carbon, acetyl carbon, and carbon nantotubes); metal particles (e.g., particles of silver, gold, platinum, iridium, platinum-iridium alloys, titanium, tungsten, stainless steel); particles of other materials (e.g., nickel, ceramics, or carbon) that are coated with metals with higher contact conductivity (e.g., silver, gold, iridium, and platinum). Further, according to various embodiments, particles of shapes and morphologies may be utilized to better facilitate electrical contact between conductive particles in the polymer. According to various embodiments utilizing polymers doped with conductive particles, conductive particles may be pre-mixed into the polymer that is subsequently formed into an electrode, may be simultaneously mixed with a polymer and dispensed to form an electrode, or may be injected into a previously dispensed polymer layer with a carrier material (e.g., toluene or alcohol).
According to various embodiments, the design and manufacturing of the flexible devices may also include: use of polymers that are made conductive by filling with conductive particles, and in which the polymer shrinks to keep conductive particles in compression; polymers that shrink, expand, and/or soften after curing or when exposed to the body, to introduce stresses and/or shape changes into the material and/or other changes in mechanical compliance; substrate layers that are stretched during application of other layers, to keep the secondary layers in compression when the substrate is relaxed; other materials and fibers (including carbon or glass fibers) embedded into the structures to provide mechanical strain reinforcement and/or affect the mechanical properties of the structure in homogeneous and complex heterogeneous arrangements; coatings (such as polyethylene glycol) that stiffen the structure to aid insertion into tissues, that soften or dissolve away over time; formation of twisted-pair cables and/or cable ground planes within the structure; use of magnetic fields to manipulate conductive polymers with particles that respond to magnetic fields; plasma cleaning or other types of surface activation and adhesion promotion methods (such as silanes or other compounds) applied to polymer layers to enhance their bonding and reduce the chances of delamination.
Multiple types of conductive polymers can be used within the same structure, depending on factors such as cost, conductivity, biocompatibility, and manufacturability for different feature sizes.
Electrode interfaces 302a-c may, in various embodiments, include geometrical and structural features for penetrating into tissues, hooking or providing mechanical fixation, or increasing the surface area of the electrode. Bonding between electrode interfaces 302b-c and internal conductive polymer traces 304b-c can be performed by the application of pressure to hold the conductive areas in contact, or by applying conductive adhesives or joining materials. These joints can also be further encapsulated with insulating polymers such as silicones to seal and/or structurally reinforce them.
Certain embodiments may utilize infrared data transmission in order to transmit data collected by electrode 600 to an external data receiver (not shown). Such embodiments may comprise materials with optical properties selected for selective transparency to certain optical or infrared signals so that the device can use these wavelengths for telemetry. For example, insulating polymer 606 may be selected so as to provide minimal attenuation to an infrared data signal generated by transceiver 620.
In one embodiment, electrode array 900 may be utilized for intracranial epilepsy monitoring. Some of the patients suffering from epilepsy that do not respond adequately to drug therapies are candidates for surgical treatment to resect or disrupt seizure foci. In preparation for such a surgery, an electrode array, such as electrode array 900, may be implanted over the focal areas for up to 30 days to accurately localize the seizure foci and minimize damage to surrounding cortical areas. According to various embodiments, electrode arrays may range in size from large grids (e.g., 9 cm×9 cm) to small strips of electrodes (e.g., 1 cm×6 cm). Additional embodiments include high density microECoG electrodes which may be present in conjunction with larger conventional cortical mapping electrodes. After implantation, lead wires 932 may connect the implanted electrode array to a neural instrumentation system (not shown), which records information regarding electrical conditions detected by the plurality of electrodes in electrode grid 930. Lead wires 932 may pass through the scalp of the patient. The use of percutaneous lead wires 932 may expose patients to a risk of infection.
The electrode grid 1030 is in electrical communication with a telemetry module 1031. Telemetry module 1031 includes an amplifier 1033, which receives and amplifies signals collected by each of the plurality of individual electrodes. Amplifier 1033, in one particular embodiment, may comprise analog amplifier components, such as those available from Intan, Technologies, LLC of Salt Lake City, Utah. Amplified signals generated by amplifier 1033 may be converted to digital signals by A/D converter 1035. According to various embodiments, A/D converter 1035 may also comprise a multiplexer configured to generate a digital output from a plurality of analog inputs.
A microprocessor unit (MCU) 1036 may receive and process the output of A/D converter 1035. According to various embodiments, MCU 1036 may comprise a commercially available microcontroller, or may comprise an application specific integrated circuit. In one particular embodiment, MCU 1036 may be embodied as a microprocessor in the TI MSP430 product family available from Texas Instruments of Dallas, Tex. In various embodiments, MCU 1036 may comprise both one-time programmable memory for core software storage and EEPROM memory for device serialization information and special feature programming.
MCU 1036 may prepare data to be transmitted by a data transceiver 1048. In one embodiment data transceiver 1048 may comprise an infrared transceiver, and infrared data may be transmitted via a Return to Zero (RZ) scheme with adaptive thresholding. If further DC balance is needed, 8B10B or Manchester codes may be utilized. All data may include error-checking codes. In an alternative embodiment, data transceiver 1048 may comprise a radio frequency data transmission system.
System 1000 may also include a receiver module 1047, which may be separated from telemetry module 1031 by the skin 1051 of the patient. Receiver module 1047 may comprise a data transceiver 1042. Receiver module 1047 and telemetry module 1031 may exchange data across the patient's skin using a bidirectional communications channel. Data received from telemetry module 1031 may include recorded data from electrode grid 1030, while data transmitted to telemetry module 1031 may comprise data to provide stimulation using electrode grid 1030.
Receiver module 1042 may further comprise a power transmitter 1046, which is coupled to a coil 1044. Coil 1044 may be inductively coupled to coil 1040. Power transferred to coil 1040 may be provided to a circuit for power recovery 1037, which may in turn provide power to A/D converter 1035 and amplifier 1033. According to various embodiments, inductive coupling between coil 1044 and coil 1040 may also be used to transmit data. Circuitry for power recovery circuit 1037 may comprise a resonant full-wave rectifier (not shown) and filter with a low drop-out linear regulator (not shown). Circuitry for power recovery 1037 may also include the ability to measure the over-voltage of the rectifier and pass the signal to MCU 1036 for sampling. This signal passed from circuitry for power recovery 1037 to MCU 1036 may be transmitted to receiver module 1047, and may allow receiver module 1047 to optimize transmitted power to minimize thermal dissipation in circuitry for power recovery 1037. This signal may also be used by the receiver module 1047 to sense coupling strength and alignment of receiver module 1047 relative to telemetry module 1031.
Receiver module 1147 may inductively provide power via a coil and may receive a data signal transmitted by telemetry module 1131. The inductive power transfer between receiver module 1147 and telemetry module 1131 may be accomplished using Class E architecture. In various embodiments, system 1100 allows for the adjustment of the carrier used by the inductive power transfer system and for the adjustment of the transmitted power. In one embodiment, an infrared detector (not shown) may be located in the center of receiver module 1147. An infrared-transparent window may be aligned over the infrared detector to provide a light path from an infrared transmitter (not shown) emitter in telemetry module 1131. In various embodiments, a coil for inductive power transfer may be constructed by winding Litz wire around a soft substructure, or the RF coil may be integrated into a flexible receiver printed circuit board. Receiver module 1147 may be fixed to the body by adhesives, compression bands, bandages, or any other methods.
In certain embodiments, an alignment indicator 1152 may be disposed on the receiver module 1147. Alignment indicator 1152 may provide an indication of the relative strength of the telemetry coupling between receiver module 1147 and telemetry module 1131. Alignment indicator 1152 may allow a clinician to find the optimal placement for the receiver module 1147. Certain embodiments may be able to tolerate alignment errors up to 1 cm from center.
Receiver module 1147 may be coupled to a power source and a neural instrumentation system by way of wire 1154. Certain embodiments may feature an interface adapter for connecting the External Transceiver to the Grapevine™ neural instrumentation system, which is available from Ripple, LLC of Salt Lake City, Utah. The Grapevine™ neural instrumentation system is available in both bedside and wearable configurations. The neural instrumentation system may provide for recording of data received by receiver module 1147.
This embodiment may be used as a blink prosthesis to restore eyelid function to patients with unilateral facial paralysis. The exogenous electrical charge it injects may functionally activate paretic or paralytic muscles to effect closure of the lid margin. The prosthesis records EMG with an array 1230 implanted in the contralateral neurologically intact hemiface to detect the onset of blink, and uses this detected signal to time stimulation via the implanted electrode array 1220 in the nonfunctioning eyelid to create a synchronous bilateral blink. Stimulation may also provide a trophic effect to permit more complete and more rapid recovery in facial paralysis patients.
At 1302, a mold may be prepared. The mold may take on a variety of shapes, as dictated by the particular application for which the device is to be utilized. The mold may be fabricated from a variety of materials, such as fluoropolymers. Alternatively, a flat plate may be used instead of a mold. The base layer of insulating polymer may be dispensed in the desired pattern and each subsequent layer following a similar pattern. Surface tension of the dispensed material may be sufficient to produce a fabricated device in a desired shape. Further, the shape of an electrode array may be adjusted at the time of implantation. For example, a surgeon may trim the electrode array in order to suit a particular application.
A base layer of insulating polymer (e.g., silicone) may be dispensed into the prepared mold, at 1304. A printed circuit board (PCB) with electronic components may be pressed into a well in the mold using an alignment fixture, level with the surrounding substrate layer at 1306. Further, at 1306, conductive polymer traces and electrode interfaces may be printed. At 1308, a second layer of insulating polymer may be printed. The second layer of insulating polymer may be applied over the signal traces and around the electrode interfaces. Partial curing and plasma surface treatments may be used between deposition steps to enhance bonding.
The following criteria may be utilized in evaluating suitable materials for use in connection with method 1300: pre-cure viscosity; surface tension for dispensing without the aid of a mold; curing properties; post-cure rigidity; adhesion between layers; ability to act as a carrier for the conductive particles.
Commercially available medical grade conductive silicones may be utilized in connection with 1300, and are available from NuSil in Carpinteria, Calif., and Creative Materials in Tyngsboro, Mass.
It will be obvious to those having skill in the art that many changes may be made to the details of the above-described embodiments without departing from the underlying principles of the invention. The scope of the present invention should, therefore, be determined only by the following claims.
The present application claims the benefit under 35 U.S.C. §119(e) of U.S. Provisional Patent Application No. 61/245,276, filed Sep. 23, 2009, titled “Thin Film Electrode and Interconnect Technology with Optional Integrated Electronics,” which application is incorporated herein by reference in its entirety.
This invention was made with U.S. Government support under contract no.: R44NS061604 awarded by National Institutes of Health. The U.S. Government has certain rights in this invention.
Number | Name | Date | Kind |
---|---|---|---|
4566464 | Piccone et al. | Jan 1986 | A |
4735208 | Wyler et al. | Apr 1988 | A |
4850359 | Putz | Jul 1989 | A |
4903702 | Putz | Feb 1990 | A |
5097835 | Putz | Mar 1992 | A |
5279305 | Zimmerman et al. | Jan 1994 | A |
5400782 | Beaubiah | Mar 1995 | A |
5433742 | Willis | Jul 1995 | A |
5456254 | Pietroski et al. | Oct 1995 | A |
5520180 | Uy et al. | May 1996 | A |
5681514 | Woody | Oct 1997 | A |
5707367 | Nilsson | Jan 1998 | A |
5843155 | Axelgaard | Dec 1998 | A |
5868136 | Fox et al. | Feb 1999 | A |
5895369 | Flower | Apr 1999 | A |
5904712 | Axelgaard | May 1999 | A |
5924983 | Takaki et al. | Jul 1999 | A |
6024702 | Iversen | Feb 2000 | A |
6091979 | Madsen | Jul 2000 | A |
6095148 | Shastri et al. | Aug 2000 | A |
6251978 | McCullough | Jun 2001 | B1 |
6259937 | Schulman et al. | Jul 2001 | B1 |
6304784 | Allee et al. | Oct 2001 | B1 |
6480743 | Kirkpatrick et al. | Nov 2002 | B1 |
6529774 | Greene | Mar 2003 | B1 |
6624510 | Chan et al. | Sep 2003 | B1 |
6643552 | Edell et al. | Nov 2003 | B2 |
6696575 | Schmidt et al. | Feb 2004 | B2 |
6792314 | Byers et al. | Sep 2004 | B2 |
6829498 | Rousche et al. | Dec 2004 | B2 |
6862479 | Whitehurst et al. | Mar 2005 | B1 |
6907299 | Han | Jun 2005 | B2 |
6973342 | Swanson | Dec 2005 | B1 |
6993392 | Nicolelis et al. | Jan 2006 | B2 |
7006859 | Osorio et al. | Feb 2006 | B1 |
7027874 | Sawan et al. | Apr 2006 | B1 |
7107097 | Stern et al. | Sep 2006 | B2 |
7162308 | O'Brien et al. | Jan 2007 | B2 |
7190989 | Swanson et al. | Mar 2007 | B1 |
7212851 | Donoghue e | May 2007 | B2 |
7229437 | Johnson et al. | Jun 2007 | B2 |
7231259 | Jenney et al. | Jun 2007 | B2 |
7234225 | Johnson et al. | Jun 2007 | B2 |
7236834 | Christopherson et al. | Jun 2007 | B2 |
7264876 | Smalley et al. | Sep 2007 | B2 |
7272427 | Ristolainen | Sep 2007 | B2 |
7330756 | Marnfeldt | Feb 2008 | B2 |
7337012 | Maghribi et al. | Feb 2008 | B2 |
7346391 | Osorio et al. | Mar 2008 | B1 |
7347826 | Karicherla et al. | Mar 2008 | B1 |
20040243204 | Maghribi et al. | Dec 2004 | A1 |
20050143790 | Kipke et al. | Jun 2005 | A1 |
20050182423 | Schulte et al. | Aug 2005 | A1 |
20050192644 | Boveja et al. | Sep 2005 | A1 |
20060058627 | Flaherty et al. | Mar 2006 | A1 |
20060129056 | Leuthardt et al. | Jun 2006 | A1 |
20060149319 | Kuo et al. | Jul 2006 | A1 |
20060224060 | Garell et al. | Oct 2006 | A1 |
20060264729 | Putz et al. | Nov 2006 | A1 |
20070123963 | Krulevitch | May 2007 | A1 |
20070167815 | Jacobsen et al. | Jul 2007 | A1 |
20080058875 | Greenberg et al. | Mar 2008 | A1 |
20080319292 | Say et al. | Dec 2008 | A1 |
20090149913 | Putz et al. | Jun 2009 | A1 |
20090254134 | Nikolov et al. | Oct 2009 | A1 |
Number | Date | Country | |
---|---|---|---|
20110237921 A1 | Sep 2011 | US |
Number | Date | Country | |
---|---|---|---|
61245276 | Sep 2009 | US |