Acoustic signal transmission couplants and coupling mediums

Abstract
Devices, systems, and methods are disclosed for use in tomographic ultrasound imaging, large aperture ultrasound imaging and therapeutic ultrasound that provide for coupling acoustic signal transducers to body structures for transmitting and receiving acoustic signals. The acoustic signal transmission couplants can conform to the receiving medium (e.g., skin) of the subject such that there is an acoustic impedance matching between the receiving medium and the transducer. In one aspect, an acoustic coupling medium includes a hydrogel including polymerizable material that form a network structured to entrap an aqueous fluid inside the hydrogel. The hydrogel is structured to conform to the receiving body, and the acoustic coupling medium is operable to conduct acoustic signals between acoustic signal transducer elements and a receiving medium when the hydrogel is in contact with the receiving body such that there is an acoustic impedance matching between the receiving medium and the acoustic signal transducer elements.
Description
TECHNICAL FIELD

This patent document relates to systems, devices, and processes for acoustic energy diagnostics and therapies.


BACKGROUND

Acoustic imaging is an imaging modality that employs the properties of sound waves traveling through a medium to render a visual image. High frequency acoustic imaging has been used as an imaging modality for decades in a variety of biomedical fields to view internal structures and functions of animals and humans. High frequency acoustic waves used in biomedical imaging may operate in different frequencies, e.g., between 1 and 20 MHz, or even higher frequencies, and are often termed ultrasound waves. Some factors, including inadequate spatial resolution and tissue differentiation, can lead to less than desirable image quality using conventional techniques of ultrasound imaging, which can limit its use for many clinical indications or applications.


SUMMARY

Techniques, systems, and devices are disclosed for coupling acoustic signal transducers to body structures for transmitting and receiving acoustic signals in ultrasound imaging, range-Doppler measurements, and therapies.


In one aspect, a couplant device of the disclosed technology for transmission of acoustic energy between transducers and a target includes a housing body structured to present an array of transducer elements on a curved section (e.g., curved lip) of the housing body (e.g., such as a semicircular or a circular portion that exposes the transducer elements of the array on a curved surface); and an acoustic coupling component including a hydrogel material (e.g., which may be at least partially contained in an outer lining). The acoustic coupling component is operable to conduct acoustic signals between a transducer element disposed in the housing body and a receiving medium (e.g., skin of a subject) in contact with the acoustic coupling component to propagate the acoustic signal toward a target volume, such that the acoustic coupling component is capable to conform to the target volume such that there is an acoustic impedance matching (e.g., very low attenuation) between the receiving medium and the transducer element.


The subject matter described in this patent document and attached appendices can be implemented in specific ways that provide one or more of the following features. For example, the couplant device can further include a flexible bracket coupled to and capable of moving with respect to the housing body, in which the flexible bracket secures the acoustic coupling component to the device. For example, the target volume includes a biological structure of a subject (e.g., an organ or tissue), and the receiving medium includes skin of the subject. In implementations of the couplant device, for example, the receiving medium can include hair on the exterior of the skin.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1A shows a schematic diagram of an exemplary acoustic couplant device of the disclosed technology.



FIG. 1B shows a three dimensional view of an acoustic couplant device of the disclosed technology.



FIG. 1C shows another three dimensional view of an acoustic couplant device of the disclosed technology.



FIG. 2A shows a schematic diagram of an exemplary acoustic coupler of the disclosed technology attached to an exemplary flexible bracket to interface to an array of transducing elements.



FIG. 2B shows a three dimensional view schematic diagram of an acoustic coupler attached to a flexible bracket in accordance with an exemplary embodiment.



FIG. 2C shows a two dimensional side view schematic diagram of an acoustic coupler attached to a flexible bracket in accordance with an exemplary embodiment.



FIG. 2D shows a cross-sectional view schematic diagram of an acoustic coupler interfaced with a transducer element in accordance with an exemplary embodiment.



FIG. 3A shows a top view schematic diagram of an acoustic couplant device of the disclosed technology to provide a complete circular ring array of transducer elements.



FIG. 3B shows a three dimensional schematic diagram of an acoustic couplant device of the disclosed technology to provide a complete circular ring array of transducer elements.



FIG. 4 shows a block diagram of an exemplary acoustic imaging and/or therapy system of the disclosed technology.



FIG. 5A shows an exemplary embodiment of an acoustic coupling medium.



FIG. 5B shows another exemplary embodiment of an acoustic coupling medium.



FIG. 5C shows another exemplary embodiment of an acoustic coupling medium.



FIG. 5D shows another exemplary embodiment of an acoustic coupling medium.



FIG. 5E shows another exemplary embodiment of an acoustic coupling medium.



FIG. 5F shows another exemplary embodiment of an acoustic coupling medium.



FIG. 5G shows another exemplary embodiment of an acoustic coupling medium.



FIG. 6 shows schematic diagrams of an exemplary acoustic coupling medium formed in various shapes, sizes, and configurations.



FIG. 7A shows schematic diagram of an exemplary embodiment of the acoustic coupling medium with an attachment component.



FIG. 7B shows front and side schematic views of an exemplary embodiment of the acoustic coupling medium with an attachment component.



FIG. 7C shows different schematic views of an exemplary embodiment of the acoustic coupling medium with a tubular curved shape.



FIG. 8 illustrates a set of operations that can be carried out to produce acoustic waveforms using an acoustic impedance matched couplant in accordance with an exemplary embodiment.





DETAILED DESCRIPTION

Acoustic imaging can be performed by emitting an acoustic waveform (e.g., pulse) within a physical elastic medium, such as a biological medium, including tissue. The acoustic waveform is transmitted from a transducer element (e.g., of an array of transducer elements) toward a target volume of interest (VOI). Propagation of the acoustic waveform in the medium toward the target volume can encounter structures that cause the acoustic waveform to become partly reflected from a boundary between two mediums (e.g., differing biological tissue structures) and partially transmitted. The reflection of the transmitted acoustic waveform can depend on the acoustic impedance difference between the two mediums (e.g., at the interface between two different biological tissue types). For example, some of the acoustic energy of the transmitted acoustic waveform can be scattered back to the transducer at the interface to be received, and processed to extract information, while the remainder may travel on and to the next medium. In some instances, scattering of the reflection may occur as the result of two or more impedances contained in the reflective medium acting as a scattering center. Additionally, for example, the acoustic energy can be refracted, diffracted, delayed, and/or attenuated based on the properties of the medium and/or the nature of the acoustic wave.


Acoustic wave speed and acoustic impedance differences can exist at the interface between the transducer and the medium to receive the acoustic waveform, e.g., referred to as the receiving medium, for propagation of the acoustic waveform toward the target volume, which can disrupt the transmission of the acoustic signal for imaging, range-Doppler measurement, or therapeutic applications. Acoustic impedance differences caused due to differing material properties (e.g., material density) of the two mediums and the acoustic wave velocity, such that a substantial amount of the emitted acoustic energy will be reflected at the interface rather than transferred in full across the interface. In typical acoustic (e.g., ultrasound) imaging or therapy applications, for example, a transmission gel is applied to the receiving medium (i.e., the skin of a subject) at the interface where the transducers will make contact to improve the transfer of the acoustic waveform(s) from the transducer to the body and the reception of the returned acoustic waveform(s) from the body back to the transducer. In such applications without the ultrasound gel, the interface may include air as a component of the medium between the receiving medium (e.g., living skin tissue) and the transducer, and an acoustic impedance mismatch in the transducer-to-air and the air-to-body discontinuity causes the scattering (e.g., reflection) of the emitted acoustic energy.


Despite relatively good success in reducing acoustic impedance difference at the interface, when applied, acoustic transmission gels may contain tiny packets of air that can disrupt the transmission of acoustic signals. Additionally, many patients complain of discomforts with the use of gels applied to their skin, e.g., such as temperature, stickiness, or other. More concerning, however, acoustic transmission gels can become contaminated during production or storage, which has led to infections within some patients. For subjects with hair on their skin at the location where the transducer is to be placed, these subjects typically must shave or otherwise remove the external hair which exasperates the trapping of air between the skin and gel.


For non-normal angles of incidence of the acoustic wave relative to the interface, the differences in the acoustic wave speed can result in refraction of the acoustic sound wave. Acoustic wave speed differences at the interface cause the propagation path of longitudinal acoustic waves to refract or change direction according to Snell's Law as a function of the angle of incidence and the acoustic wave speeds either side of the interface. Accumulations of infinitesimal amounts of refraction as the wave propagates in a heterogeneous material results in bending or curvature in the path of the acoustic wave.


As conventional ultrasound imaging assumes that acoustic waves travel in straight lines, refraction along the acoustic path causes degradation and distortion in the resulting image due the ambiguity it creates for the arrival time and location of an acoustic waveform in space for both transmission and reception. A material that matches the acoustic wave speed at the interface significantly reduces the effects of refraction, resulting in a clearer and less ambiguous image. Additionally, a material that has a homogeneous acoustic wave speed throughout will minimize the potential for curvature of acoustic wave paths inside the material.


Disclosed are techniques, systems, and devices for coupling acoustic signal transducers to body structures for transmitting and receiving acoustic signals in ultrasound imaging, range-Doppler measurements, and therapies. The disclosed acoustic signal transmission couplants can conform to the receiving medium (e.g., skin) of the subject such that there is an acoustic impedance matching between the receiving medium and the transducer.


Disclosed are also various embodiments of an acoustic coupling medium including a hydrogel formed from one or more polymerizable materials and capable of conforming or molding into specific three dimensional shapes for use in tomographic ultrasound imaging, large aperture ultrasound imaging, and therapeutic ultrasound.


In one embodiment, a couplant device of the disclosed technology for transmission of acoustic energy between transducers and a target includes a housing body including a curved surface on which an array of transducer elements may be disposed; and an acoustic coupling component including a hydrogel material, in which the acoustic coupling component is operable to conduct acoustic signals between a transducer element disposed in the housing body and a receiving medium (e.g., skin of a subject) in contact with the acoustic coupling component to propagate the acoustic signal toward a target volume, such that the acoustic coupling component is capable to conform to the receiving medium such that there is an acoustic impedance matching between the receiving medium and the transducer element. In some embodiments, the couplant device can further include a flexible bracket coupled to and capable of moving with respect to the housing body, in which the flexible bracket secures the acoustic coupling component to the device. For example, the target volume includes a biological structure of a subject (e.g., an organ or tissue), and the receiving medium includes skin of the subject. In implementations of the couplant device, for example, the receiving medium can include hair on the exterior of the skin.



FIG. 1A shows a two dimensional side view schematic diagram and FIGS. 1B and 1C show three dimensional views of an acoustic couplant device 100 of the disclosed technology. The couplant device 100 includes a housing structure 101 to contain and position transducers for transmitting and receiving acoustic signals to/from a mass to which the acoustic couplant device 100 is applied. The housing structure 101 includes a curved section where transducer elements 110 of an acoustic transmit and/or receive transducer array are positioned, e.g., which is shown in FIG. 1C. The curved section of the housing structure 101 can be configured to various sizes and/or curvatures tailored to a particular body region or part where the couplant device 100 is to be applied in acoustic imaging, measurement, and/or therapy implementations. For example, the length, depth, and arc of the curved section of the housing structure 101 can be configured to make complete contact with a region of interest on an anatomical structure, e.g., such as a breast, arm, leg, neck, throat, knee joint, hip joint, ankle, waist, shoulder, or other anatomical structure of a human or animal (e.g., canine) subject to image or apply ultrasonic treatment to target volumes within such structures, such as splenic masses, cancerous or noncancerous tumors, legions, sprains, tears, bone outlines and other signs of damage or maladies. For example, the curved section of the housing structure 101 can include an aperture length in a range of a few centimeters to tens or hundreds of centimeters (e.g., such as an 18 cm baseline as depicted in FIG. 1A), an aperture depth in a range of a few centimeters to tens or hundreds of centimeters, and an arc or curvature of 1/(half or a few centimeters) to 1/(tens or hundreds of centimeters), e.g., 1/0.5 cm−1 to 1/18 cm−1. The couplant device 100 includes an acoustic coupler 105 attached to the housing structure 101 such that the acoustic coupler 105 is in contact with the external surface area of the transducer elements 110 disposed in the housing structure 101.


For example, the acoustic coupler 105 can be attached to the housing structure 101 by molding the hydrogel material against the curved section of the housing structure 101 to directly couple the acoustic coupler 105 and the transducer elements 110 at an interface. In such implementations, the housing structure 101 can include a securement mechanism (e.g., such as a clip) at various locations at the curved section to secure the molded acoustic coupler 105 to the housing structure 101, in which the securement mechanism is located on the housing structure 101 at locations away from the transducer elements 110 to not interfere with acoustic signal propagation transmitted and received by the transducer elements. In addition, or alternatively, for example, the housing structure 101 and/or the acoustic coupler 105 can include an adhesive portion to attach the molded acoustic coupler 105 to the curved section of the housing structure 101. In some implementations, for example, the adhesive portion can be configured as an adhesive layer attached to the receiving surface of the curved section of the housing structure 101 and/or an outer portion of the acoustic coupler 105. In some implementations, for example, the adhesive portion can include pretreatment of the outer portion areas of the hydrogel material of the acoustic coupler 105 (e.g., such as applying a low pH solution) to cause such areas to become naturally adhesive.


In some implementations, the acoustic coupler 105 includes a hydrogel material engineered to conduct acoustic signals between transducer elements 110 and a receiving medium (e.g., body region or part of the subject, e.g., such as the subject's midsection, head, or appendage) where the couplant device 100 is to be placed in contact to transmit and receive the acoustic signals propagating toward and from a target volume of interest in the subject. The acoustic coupler 105 is able to conform to the receiving medium to provide acoustic impedance matching between the transducer elements and the receiving medium (e.g., the skin of the subject, including body hair protruded from the skin).


The hydrogel material can be configured to have a selected thickness based on the size of the receiving body of the subject or object of the acoustic imaging, measurement, or therapy application. The diagram of FIG. 1A depicts the acoustic coupler 105 having various thicknesses L1, L2, L3, and L4 with respect to dimensions of the curved section of the housing structure 101. For example, in some embodiments, the L1 thickness can be 4 cm, the L2 thickness can be 6 cm, the L3 thickness can be 8 cm, and the L4 thickness can be 10 cm, e.g., in which the curved section of the housing structure 101 includes a semicircular geometry with a 12 cm radius. In some implementations, for example, the hydrogel material of the acoustic coupler 105 can include polyvinyl alcohol (PVA). In some implementations, for example, the hydrogel material can include polyacrylamide (PAA), which can include alginate. In some embodiments, for example, the acoustic coupler 105 can include an outer lining to encase at least some portions of the hydrogel. The exemplary outer lining can be formed over regions of the hydrogel that are in contact with the housing structure 101. In some implementations, for example, the exemplary outer lining can be configured to fully encase the hydrogel material to produce a pad. The hydrogel can flex, stretch and conform to any complex geometry surface to enable very low loss and a highly matched impedance path for efficient transmission of acoustic waveforms (e.g., ultrasonic waves) into tissue of the subject, e.g., including a human or any other animal. For example, the hydrogel can include a material structure that allows acoustic signal propagation with an attenuation factor of 0.1 dB/MHz2·cm or less, an impedance of 1.5 MRayls or less, and a longitudinal speed of sound of 1540 m/s at 20° C. The acoustic coupler 105 is engineered to have a % elongation of 1000% or greater, a density of 1.00 g/cm3±0.05 g/cm3, a shear modulus of 1 MPa, and melting and freezing point of 70° C. and −5° C., respectively. For example, the hydrogel material can be at least 95% water and have a pH of −7.0.


In some embodiments of the acoustic coupler 105, for example, one side of the hydrogel and/or outer lining is configured to have a tacky surface to contact the transducer elements 110 to promote adherence to the transducer face such that air or other substances are prohibited from becoming entrapped once the couplant device 100 is applied.


In some embodiments of the couplant device 100, for example, the housing structure 101 includes a flexible bracket 102 that attaches to the curved section of the housing structure 101 body. In some implementations, for example, the acoustic coupler 105 can be molded into the flexible bracket 102, which can also include the acoustic coupler 105 being adhesively attached (e.g., glued) to the flexible bracket 102 at portions of the acoustic coupler 105 away from acoustic signal propagation with the transducer elements. The flexible bracket 102 is structured to flex such that it can conform to the receiving body that it surrounds. For example, the flexible bracket 102 can include flexible materials, e.g., including, but not limited to, ABS plastic, polyurethane, nylon, and/or acetyl copolymer. FIGS. 2A-2D shows schematic diagrams of the acoustic coupler 105 attached to the flexible bracket 102.



FIG. 2A shows a three dimensional view schematic diagram of the acoustic coupler 105 attached to the flexible bracket 102. The flexible bracket 102 can be structured to include a base component 112 to attach to the ends of the acoustic coupler 105. For example, base component 112 can include clips to secure and/or adhere the acoustic coupler 105. In some embodiments, for example, the flexible bracket 102 can include one or more arch components 113 configured to a size and curvature to span across the curved section of the housing structure 101 and positioned at one or more respective locations on the base component 112 away from where the transducer elements 110 are positioned when the flexible bracket 102 is attached to the housing structure 101. The flexible bracket 102 can be structured to have pattern of notches 114 on one side of the arch component(s) 113 to allow the flexible bracket 102 to bend easily without breaking. On the other side of the arch component(s) 113, the flexible bracket 102 can include an undercut lip with a chamfer so that when it's flexed into the shape of the array and pressed into position, the chamfered lip flexes over the lip on the curved section of the housing structure 101 and secures the flexible bracket 102, and thereby the acoustic coupler 105, in place. For example, the acoustic coupler 105 can be bonded or molded into the flexible bracket 102 when cross-linking of the hydrogel occurs. In some implementations, for example, the hydrogel of the acoustic coupler 105 can also be molded on the subject-facing side to smooth or curve the edges, e.g., which can allow the device 100 to contact and release from the subject easier. FIG. 2B shows a three dimensional view schematic diagram of the acoustic coupler 105 attached to the flexible bracket 102, and FIG. 2C shows a two dimensional side view schematic diagram of the acoustic coupler 105 attached to the flexible bracket 102.



FIG. 2D shows a cross-sectional view schematic diagram of the acoustic coupler 105 interfaced with a transducer element 110 and attached to the housing structure 101 via the flexible bracket 102. As shown in this diagram, the acoustic coupler 105 conforms directly onto the face of the transducer element 110. In this example, the acoustic coupler 105 is attached to the clip components of the flexible bracket 102 by an adhesive on the external surface of the clips, e.g., to align in contact with the ‘tacky regions’ of the hydrogel and/or outer lining of the acoustic coupler 105. The clips attaches around the lip of the housing body 101 to provide direct contact between the acoustic coupler 105 and the face of the transducer element 110. As shown in the diagram, the transducer element 110 includes a transducer acoustic backing portion that interfaces with electrical communication elements for transduction of electrical to/from acoustic energy.


In some implementations of the couplant device 100, for example, the surface of the acoustic coupler 105 in contact with the subject can be lubricated so it can slide over the skin easily without trapping air bubbles for optimum acoustic transmission. Examples of such lubricants can include treating the side of the hydrogel material that is to be in contact with the subject with degassed and/or deionized water to render that portion of the hydrogel material highly lubricated.


Referring back to FIGS. 1A-1C, the housing structure 101 can include one or more handles to provide a place for a user to hold the couplant device 100 and/or move the couplant device 100 for positioning on the receiving body (e.g., a subject's torso, head, appendage, etc.) for an acoustic measurement or therapy. The housing structure 101 can include openings at various locations on the exterior of the housing structure 101 that provide access to the interior (e.g., including interior compartments) where electronic components including the transducer elements of the transducer array are located within the housing structure 101. For example, as depicted in FIG. 1A, an electrical cable or wires can be electrically connected to the electronics contained within the housing structure 101 for data communication and/or power supply. For example, the housing structure 101 can include compartments to secure signal conditioning and/or multiplexing circuitry in communication with the transducer elements 110, e.g., L0 transducer electronics, L1 A transducer electronics and multiplexing circuitry (e.g., multiplexing board type A), L1 B transducer electronics and multiplexing circuitry (e.g., multiplexing board type B), and/or L2 transducer level 2 MUX rigid flexible circuit card and flex mezzanine board. In some implementations, for example, the couplant device 110 includes a multiplexing unit contained in an interior compartment of the housing structure 101 and in communication with the transducer elements 110 to select one or more transducing elements 110 of the array to transmit individual acoustic waveforms, and to select one or more transducing elements 110 of the array to receive the returned acoustic waveforms. In some implementations of the couplant device, for example, the device 100 includes a data processing unit contained in a compartment in the housing structure 101 that includes signal conditioning circuitry to amplify the electrical signals transduced from the returned acoustic signals, and/or electrical signals to be transduced to the transmitted acoustic signals. In some embodiments of the exemplary data processing unit, for example, the data processing unit can include a processor and a memory to process and store data, respectively, which can be in communication with an input/output (I/O) unit to interface to transmit and receive data from an acoustic imaging and/or therapy system for controlling operations of the data processing unit of the device 100. In some implementations, for example, the data processing unit is in communication with the exemplary multiplexing unit.


As depicted in FIG. 1C, which shows the flexible bracket 102 attached to the transducer housing structure 101 without the acoustic coupler 105 presently attached, the transducer elements 110 can be arranged in a semicircular configuration to span along at least part of the curved section of the housing structure 101. The array of transducing elements 110 are presented on the curved geometry of this section of the housing structure 101 to be in direct contact with the acoustic coupler 105 to transmit and receive acoustic signals. In the exemplary embodiment shown, the transducer elements 110 are disposed on a lip of the curved section of the housing structure 101. Based on the flexibility, stretchability, and conformability of the acoustic coupler 105, the acoustic coupler 105 can remain in contact with the transducer elements 110 during application of the couplant device 100 as it is positioned and moved along the body structure of the subject. For example, the transducer elements 110 are arranged on the curved section (e.g., such as a semicircular ring, or a complete circular ring) of the housing structure 101. The flexible bracket 102 can include clips to attach to the lip 111 of the curved section. In some implementations, for example, the flexible bracket 102 can also include clips to secure the acoustic coupler 105 to the flexible bracket 102, which provides direct contact of the acoustic coupler 105 on to the face of the transducer elements 110 on the housing structure 101.



FIGS. 3A and 3B show a top view schematic diagram and three dimensional schematic diagram, respectively, of an acoustic couplant device 300 of the disclosed technology to provide a complete circular ring array of transducer elements 110. The couplant device 300 includes a housing structure 301 having a circular section to contain and position the transducer elements 110 for transmitting and receiving acoustic signals to/from a mass to which the acoustic couplant device 300 is applied. For example, the circular section of the housing structure 301 can include a circle geometry, elliptical geometry, or other curved geometry. The circular section of the housing structure 301 can be configured to various sizes and/or curvatures tailored to a particular body region or part where the couplant device 300 is to be applied in acoustic imaging, measurement, and/or therapy implementations. For example, the length, depth, and geometry of the circular section of the housing structure 301 can be configured to make complete contact, e.g., which can completely surround or enclose, with a region of interest on an anatomical structure of a subject, e.g., such as a breast, of a human or animal (e.g., canine) to image or apply ultrasonic treatment to target volumes within the structure. The couplant device 300 includes the acoustic coupler 105 attached to the housing structure 301 such that the acoustic coupler 105 is in contact with the external surface area of the transducer elements 110 disposed in the circular section of the housing structure 301.


The couplant device 300 can include a flexible bracket 302 to attach to the circular section of the housing structure 301 body to couple the acoustic coupler 105 to the transducer elements 110 housed in the housing structure 301. In some implementations, for example, the acoustic coupler 105 can be molded into the flexible bracket 302, which can include the acoustic coupler 105 being adhesively attached to the flexible bracket 302 at portions of the acoustic coupler 105 away from acoustic signal propagation with the transducer elements.



FIG. 4 shows a block diagram of an acoustic imaging system 400 in communication with the acoustic couplant device 100 for acoustic imaging, range-Doppler measurements, and/or therapeutic application of acoustic energy of a target volume in a receiving body (e.g., anatomical structure of a human or non-human animal subject) to which the acoustic couplant device 100 is applied. Examples of acoustic systems, devices, and methods for acoustic imaging, range-Doppler measurements, and therapies are described in U.S. Pat. No. 8,939,909, titled “Spread Spectrum Coded Waveforms in Ultrasound Imaging,” and U.S. Patent Application Publication No. 2015/0080725, titled “Coherent Spread-Spectrum Coded Waveforms in Synthetic Aperture Image Formation,” both of which are incorporated by reference in this patent document. In some implementations, such acoustic systems can generate, transmit, receive, and process arbitrary or coded acoustic waveforms that create a large, synthetic aperture. For example, coherent, spread-spectrum, instantaneous-wideband, coded waveforms can be produced in synthetic aperture ultrasound (SAU) applications using such acoustic systems, e.g., employing the disclosed acoustic coupling medium.


Referring to FIG. 4, the system 400 can include systems and/or devices described in the '909 patent and the '725 patent publication. The system 400 can be used to produce acoustic waveforms transduced by the device 100 (or the device 300) for transmission toward the target volume (and reception of returned acoustic waveforms), such that the acoustic waveforms have enhanced waveform properties that include a spread-spectrum, wide instantaneous bandwidth, coherency, pseudo-random noise characteristics, and frequency- and/or phase-coding. In some implementations, the system 400 can be used to produce acoustic waveforms across an expanded effective (synthetic) aperture using the device 100 (or the device 300) for transmission toward the target volume (and reception of returned acoustic waveforms), in which the acoustic waveforms have enhanced waveform properties including a spread-spectrum, wide instantaneous bandwidth, coherent, pseudo-random noise characteristics, and coding.


EXAMPLES

The following examples are illustrative of several embodiments of the present technology. Other exemplary embodiments of the present technology may be presented prior to the following listed examples, or after the following listed examples.


In one example of the present technology (example 1), a couplant device for transmission of acoustic energy between transducers and a target includes an array of transducer elements to transmit acoustic signals toward a target volume and to receive returned acoustic signals that return from at least part of the target volume; a housing body including a curved section on which the array of transducer elements are arranged; and an acoustic coupling component including a hydrogel material, the acoustic coupling component operable to conduct the acoustic signals between a transducer element disposed in the housing body and a receiving medium in contact with the acoustic coupling component to propagate the acoustic signals toward the target volume, in which the acoustic coupling component is capable to conform to the receiving medium and the transducer element such that there is an acoustic impedance matching between the receiving medium and the transducer element.


Example 2 includes the device of example 1, in which the device further includes a flexible bracket coupled to and capable of moving with respect to the housing body, in which the acoustic coupling component is attached to the flexible bracket.


Example 3 includes the device of example 1, in which the hydrogel material includes polyvinyl alcohol (PVA).


Example 4 includes the device of example 1, in which the hydrogel material includes polyacrylamide (PAA).


Example 5 includes the device of example 4, in which the hydrogel material includes alginate.


Example 6 includes the device of example 1, in which the acoustic coupling component includes an outer lining at least partially enclosing the hydrogel material.


Example 7 includes the device of example 1, in which the acoustic coupling component is operable to propagate the acoustic signals with an attenuation factor of 0.1 dB/MHz2·cm or less, or with an impedance of 1.5 MRayls or less.


Example 8 includes the device of example 1, in which the acoustic coupling component is capable to undergo a % elongation of 1000% or greater, or includes a shear modulus of 1 MPa.


Example 9 includes the device of example 1, in which the target volume includes a biological structure of a living subject and the receiving medium includes an anatomical structure of the living subject.


Example 10 includes the device of example 9, in which the curved section of the housing body includes a curvature to facilitate complete contact with the anatomical structure, such that the acoustic coupling component is in direct contact with skin of the anatomical structure.


Example 11 includes the device of example 10, in which the anatomical structure includes hair on the exterior of the skin.


Example 12 includes the device of example 9, in which the anatomical structure includes a breast, an arm, a leg, a neck including the throat, a knee joint, a hip joint, an ankle joint, an elbow joint, a shoulder joint, an abdomen, or a chest, or a head.


Example 13 includes the device of example 9, in which the biological structure includes a cancerous or noncancerous tumor, an internal legion, a connective tissue sprain, a tissue tear, or a bone.


Example 14 includes the device of example 9, in which the subject includes a human or a non-human animal.


Example 15 includes the device of example 1, in which the curved section of the housing body includes a semicircular geometry.


Example 16 includes the device of example 1, in which the curved section of the housing body includes a 360° circular geometry, and the array of transducer elements arranged along the 360° circular section of the housing body.


Example 17 includes the device of example 16, in which the 360° circular section of the housing body and the acoustic coupling component provide a curvature to facilitate complete contact around an anatomical structure of a living subject, and in which the device is operable to receive the returned acoustic signals from the target volume such that an acoustic imaging system in data communication with the device is able to produce a 360° image of the target volume.


Example 18 includes the device of example 1, in which the device further includes a multiplexing unit contained in an interior compartment of the housing body and in communication with the array of transducer elements to select one or more transducing elements of the array to transmit individual acoustic waveforms, and to select one or more transducing elements of the array to receive the returned acoustic waveforms.


In one example of the present technology (example 19), an acoustic waveform system includes a waveform generation unit, an acoustic signal transmission couplant, a multiplexing unit, and a controller unit. The waveform generation unit includes one or more waveform synthesizers coupled to a waveform generator, in which the waveform generation unit is operable to synthesize a composite waveform that includes a plurality of individual orthogonal coded waveforms corresponding to different frequency bands that are generated by the one or more waveform synthesizers according to waveform information provided by the waveform generator, in which the individual orthogonal coded waveforms are mutually orthogonal to each other and correspond to different frequency bands, such that each of the individual orthogonal coded waveforms includes a unique frequency with a corresponding phase. The acoustic signal transmission couplant includes a housing body including a curved section on which transducer elements are arranged; an array of transducer elements to transmit acoustic waveforms corresponding to the individual orthogonal coded waveforms toward a target volume and to receive returned acoustic waveforms that return from at least part of the target volume; and an acoustic coupling component including a hydrogel material, the acoustic coupling component operable to conduct the acoustic waveforms between a transducer element disposed on the housing body and a receiving medium in contact with the acoustic coupling component, in which the acoustic coupling component is capable to conform to the receiving medium and the transducer element such that there is an acoustic impedance matching between the receiving medium and the transducer element. The multiplexing unit is in communication with the array of transducer elements and operable to select one or more transducing elements of an array to transduce the individual orthogonal coded waveforms into the corresponding acoustic waveforms, and operable to select one or more transducing elements of the array to receive the returned acoustic waveforms. The controller unit, which is in communication with the waveform generation unit and the multiplexing unit, includes a processing unit to process the received returned acoustic waveforms to produce a data set including information of at least part of the target volume.


Example 20 includes the system of example 19, further including an array of analog to digital (A/D) converters to convert the received returned acoustic waveforms received by the array of transducer elements of the acoustic signal transmission couplant from analog format to digital format as a received composite waveform that includes information of at least part of the target volume.


Example 21 includes the system of example 19, further including a user interface unit in communication with the controller unit.


Example 22 includes the system of example 19, in which the produced data set includes an image of at least part of the target volume.


Example 23 includes the system of example 19, in which the acoustic signal transmission couplant includes a flexible bracket coupled to and capable of moving with respect to the housing body, in which the acoustic coupling component is attached to the flexible bracket.


Example 24 includes the system of example 23, in which the hydrogel material includes at least one of polyvinyl alcohol (PVA), polyacrylamide (PAA), or PAA with alginate.


Example 25 includes the system of example 19, in which the curved section of the housing body of the acoustic signal transmission couplant includes a semicircular geometry, or the curved section of the housing body of the acoustic signal transmission couplant includes a 360° circular geometry such that the array of transducer elements are arranged along the 360° circular section of the housing body.


Example 26 includes the system of example 25, in which the 360° circular section of the housing body and the acoustic coupling component provide a curvature to facilitate complete contact around an anatomical structure of a living subject, and in which the device is operable to receive the returned acoustic waveforms from the target volume such that the system is able to produce a 360° image of the target volume.


In one example of the present technology (example 27), a method of producing acoustic waveforms using an acoustic impedance matched couplant includes: synthesizing, in one or more waveform synthesizers, one or more composite waveforms to be transmitted toward a target, in which a composite waveform is formed of a plurality of individual orthogonal coded waveforms that are mutually orthogonal to each other and correspond to different frequency bands, such that each of the individual orthogonal coded waveforms includes a unique frequency with a corresponding phase; transmitting, from one or more transmitting positions relative to the target using an array of transducing elements of an acoustic signal transmission couplant, one or more composite acoustic waveforms that includes a plurality of acoustic waveforms, in which the transmitting includes selecting one or more of the transducing elements of the array to transduce the plurality of individual orthogonal coded waveforms of the respective one or more composite waveforms into the plurality of corresponding acoustic waveforms of the respective one or more composite acoustic waveforms; and receiving, at one or more receiving positions relative to the target, returned acoustic waveforms that are returned from at least part of the target corresponding to the transmitted acoustic waveforms, in which the receiving includes selecting at least some of the transducing elements of the array to receive the returned acoustic waveforms, in which the transmitting positions and the receiving positions each include (i) spatial positions of the array of transducer elements relative to the target and/or (ii) beam phase center positions of the array, in which the acoustic signal transmission couplant includes an acoustic coupling component including a hydrogel material operable to conduct the acoustic waveforms between the transducer elements and a receiving medium in contact with the acoustic coupling component, in which the acoustic coupling component is capable to conform to the receiving medium and the transducer element such that there is an acoustic impedance matching between the receiving medium and the transducer element, and in which the transmitted acoustic waveforms and the returned acoustic waveforms produce an enlarged effective aperture.


Example 28 includes the method of example 27, further including processing the received returned acoustic waveforms to produce an image of at least part of the target.


As noted earlier, some of the disclosed embodiments relate to an acoustic coupling medium including a hydrogel formed from one or more polymerizable materials and capable of conforming or molding into specific three dimensional shapes for use in tomographic ultrasound imaging, large aperture ultrasound imaging, and therapeutic ultrasound.


Hydrogel materials contain mostly water, thus, the acoustic wave speed of the hydrogel is dominated by water. The acoustic wave speed in water is approximately proportional to temperature through a high order empirically-determined polynomial relationship from 0 to 100° C. The acoustic wave speed of pure water varies from 1482 m/s to 1524 m/s from 20° C. to 37° C., respectively. Thus, the acoustic wave speed in a polymeric material will vary with temperature.


A material with a calibrated acoustic wave speed may be used in combination with a delay-and-sum beamformer to correct the propagation times on transmission and reception in order to reduce image distortion created by uncalibrated coupling materials. For example, the location of a structure such as a tissue-bone interface is ambiguous without knowledge of the average acoustic wave speed between the array and the bone. The true location of the bone may be deeper or shallower than it measures on the ultrasound image.


A material with a temperature calibrated acoustic wave speed such that the material may be heated in order to provide a more comfortable interface to the patient without creating image distortion. Besides patient comfort, a heated material also supports increased blood flow in the region in contact with the patient and in regions peripheral to the region in contact, thus facilitating more accurate Doppler measurements. A material with a calibrated acoustic wave speed will also function optimally at a target temperature (e.g. 37° C.) or target range of temperatures (e.g. 20-37° C.).


Thermocouples, thermistors, fiber-optic thermometers or other temperature sensing devices may be implanted into the hydrogel to provide real-time temperature feedback. Additionally, wires, resistors, thermopiles, electrical current, infrared radiation, water pipes, conduction, or other means to heat the hydrogel may be utilized to heat the gel. A temperature feedback and control device may be utilized to precisely and accurately control the temperature of the hydrogel.


The disclosed acoustic coupling medium can be employed in acoustic imaging, range-Doppler measurement, and therapeutic systems to transfer emitted and returned acoustic waveforms between such acoustic systems and a receiving medium, such as tissue of a living organism.


In some implementations of the disclosed acoustic coupling technology, for example, a hydrogel acoustic coupling medium of the present technology can provide spatially-varying acoustic absorption for use with acoustic imaging, diagnostic and/or therapeutic devices or systems to provide tomographic ultrasound imaging, large aperture ultrasound imaging arrays, and therapeutic ultrasound arrays for such acoustic devices and systems. In some implementations of the disclosed technology, the hydrogel acoustic coupling medium can couple acoustic waves from acoustic energy sources into the hydrogel acoustic coupling medium and subsequently into secondary media with acoustic sound speeds ranging from 1400 m/s up to 1700 m/s. Examples of the secondary media include, but are not limited to, mammalian tissues and water. The secondary media may contain structures with sound speeds outside the sound speed range of the coupling medium, e.g., such as bone, implanted devices, plastics, ceramics, glass, and metals.


In practical applications of ultrasound imaging, particularly for imaging human and nonhuman animals, ultrasound image formation typically occurs in the near field of an acoustic emission aperture, which poses several challenges for obtaining high resolution and quality ultrasound images. For example, in such ultrasound imaging applications, generally, one or more transducer elements are included in an acoustic imaging device, forming an array, to generate the acoustic aperture. These transducer elements typically require several wavelengths to transition from the near field to the far field regime following an acoustic emission, thus requiring an acoustic buffer region, also known as an acoustic standoff. For example, this acoustic buffer region or acoustic standoff may be necessary for image formation close to the acoustic aperture. Furthermore, focused image formation typically requires that the ratio of the focal depth divided by the aperture size (e.g., also known as the f-number) be greater than one, e.g., for points of the image formation closest to the acoustic aperture. Likewise, the acoustic standoff is necessary for image formation close to the acoustic aperture in order to satisfy the f-number condition.


In implementations of the disclosed technology, the image formation is generated using combinations of the transducer elements, in which a selected group of transducer elements are used to produce an acoustic emission followed by reception of return acoustic echoes on some, the same, and/or other transducer elements of the group. For example, the transducer elements producing the acoustic emission are referred to as transmit elements. Likewise, the transducer elements that receive the return acoustic echoes are referred to as receive elements. In some examples, the combinations may be divided into combinations of individual pairs of transmit and receive elements such that the linear combination of the pairs produces an approximately equivalent image as obtained using the combinations of one or more elements on both transmit and receive. For example, each time sample of an echo recorded from the pair of transmit and receive elements is an integration of acoustic reflectivity over the corresponding round-trip time or time delay corresponding to the time sample. The integration is a line integral over linear paths of the constant round-trip time or time delay. The linear paths can be circular or elliptical as determined by the location of the pair of transmit and receive elements. In practice, for example, the circular or elliptical paths may extend to highly reflective interfaces including, but not limited to, the interface between the acoustic coupling medium and a low acoustic impedance material, e.g., such as air or plastic, or the interface between the acoustic coupling medium and a high acoustic impedance material, e.g., such as metal or ceramic.


Acoustic reflections from the interfaces, also known as specular reflections, contaminate the line integrals of reflectivity and the corresponding echo samples obtained from the transmit and receive combinations. In general, for the acoustic reflections observed for the combination of transmit and receive elements, the angle of incidence measured from the transmit element to a point on the reflective interface to the surface normal vector for a point lying on the reflective interface equals the angle of reflection measured from the same normal vector to the vector defined by the point on reflective interface to the receive element. The acoustic reflection can have mirror or amphichiral symmetry. The acoustic reflection has power equal to the acoustic impedance of the secondary medium minus the acoustic impedance of the coupling medium, divided by the acoustic impedance of the secondary medium plus the acoustic impedance of the coupling medium, as described in Equation (1).










P
r

=


(


Z

2

m


-

Z
cm


)


(


Z

2

m


+

Z
cm


)






(
1
)








The contamination caused by the acoustic reflection can preclude the use of the transmit and receive combinations in beamformers based on delayed and summed echo samples, also known as a delay-and-sum beamformer. Such preclusion of echo samples can result in removal of the transmit and receive combination from the delay-and-sum beamformer, thus limiting the quality of the image pixel corresponding to the delay-and-sum beamformer. The image pixel quality is a function of the point-spread-function of the limited set of transmit and receive combinations. Such preclusion of echo samples can also reduce the signal-to-noise ratio (SNR) for the image pixel. Additionally, for the apertures with an array pitch greater than one-half wavelength, the image pixel locations that require transmitter and receiver combinations to steer away from zero degrees (0°) will be increasingly subject to grating lobes with increasing steering angle and increasing array pitch. Such grating lobes add to the sensitivity and complexity of the specular reflections.


The acoustic coupling medium of the disclosed technology can be configured in an acoustic couplant device and operable to conduct acoustic signals between a transducer element disposed in a housing body of the couplant device and a receiving medium (i.e., the secondary medium, e.g., skin of a subject) in contact with the acoustic coupling medium to propagate the acoustic signal toward a target volume. The disclosed acoustic coupling medium is capable to conform to the target volume such that there is an acoustic impedance matching (e.g., very low reflection) between the receiving medium and the transducer element.


The disclosed acoustic coupling medium is configured to have three-dimensional shape. In some examples of the disclosed acoustic coupling medium, for example, an acoustic coupling medium is engineered into a specific three-dimensional shape for a particular implementation utility, e.g., for tomographic acoustic imaging, large aperture acoustic imaging, and/or therapeutic acoustic treatment. In one example embodiment shown in FIG. 5A, an acoustic coupling medium 505A includes shape of a tube with an inner radius, an outer radius, and a height. The tubular acoustic coupling medium 505A includes a hydrogel including one or more polymerizable materials and capable of conforming or molding into specific three dimensional shapes for desired applications. The radii and the height of the acoustic coupling medium 505A can vary based on each application. For example, due to the elasticity and tensile strength of the coupling medium 505A, the tubular shape is flexible and capable of stretching around irregularly shaped secondary media, e.g., such as limbs of a human or nonhuman animal. As shown in FIG. 5A, the acoustic coupling medium 505A is attached to the housing body 501 of an acoustic couplant device. The acoustic coupling medium 505A is configured such that, when placed in contact with a subject, the coupling medium 505A also maintains constant contact with the secondary media of the subject, e.g., maintaining complete contact with the subject's skin, including around irregular structures such as elbows and knees.


Additionally, the tubular coupling medium is compatible with tomographic apertures ranging from 0 to 360 degrees around the secondary medium, e.g., subject's limbs, torso, head, etc., while maintaining acoustic contact over the entire aperture and secondary medium, simultaneously. With applied force, constant contact may be maintained with movement of the aperture over the coupling medium. For example, the tomographic apertures with a polygon shape, the flexible coupling medium maintains contact over the surface of the entire aperture, including between facets of the polygon. The exemplary tubular shape of the acoustic coupling medium 505A may be molded to match any three-dimensional shape of the aperture, including polygon shapes. For example, for tomographic apertures less than 360 degrees, the exemplary tubular acoustic coupling medium 505A does not have highly reflective air interfaces at sharp edges that would exist for coupling media extending only over the aperture. At the edges of the aperture, the transmit and receive combinations are able to function unrestricted by the tubular coupling medium 505A, thus obviating the need for preclusion of the combination from the beamformer. The reflective air interface extending around the entire coupling medium keeps wide angle and primary reflections internally reflecting around the acoustic coupling medium 505A, where they are attenuated and end up being incoherent acoustic noise.



FIG. 5B shows another arrangement of the exemplary tubular acoustic coupling medium 505A placed in contact with a body portion of the subject to conform with complete contact with the secondary medium. The example arrangement shown in FIG. 5B provides the ability for the internal reflections to be further broken up by one or more gaps in the tubular acoustic coupling medium 505A.



FIG. 5C shows another example embodiment of an acoustic coupling medium 505C that includes the hydrogel and an acoustically attenuating region in one or more portions of the hydrogel. For example, in acoustic transmission operations, the internal reflections may be absorbed with the acoustically attenuating region in the tubular acoustic coupling medium 505C. For example, such attenuation may be obtained through absorption or scattering or both. The acoustic attenuation region can be structured to include one or more of higher density polymers, higher absorption polymers, scatterers, microbubbles, microballoons, plastics, rubbers, or other absorptive materials.



FIG. 5D shows another example embodiment of an acoustic coupling medium 505D that includes the hydrogel and configured in a flattened shape convertibly adapted to a tubular shape. For example, the tubular shape may be formed from a rectangular block of the acoustic coupling medium 505D, which is wrapped around the secondary medium (e.g., of the subject). The wrapped coupling medium may be trimmed using a cutting device and attached end-to-end with an attachment device, e.g., including, but not limited to, straps, velcro, buttons, zipper, latch, gripper, or some other mechanical attachment device, or a chemical bond. FIG. 5E shows an example of the shape convertible acoustic coupling medium 505D conformed around a body portion of a subject and attached at contactable ends by an attachment component.


In addition to a tubular shape, the acoustic coupling medium may be shaped with a partial tubular shape of less than 360 degrees in the transverse plane, such that it can partially cover the secondary medium of the subject, e.g., subject's limbs, torso, head, etc., and can extend up to or beyond the boundaries of the aperture, as shown in FIG. 5F. FIG. 5F shows another example embodiment of an acoustic coupling medium 505F that includes the hydrogel and configured in a partial tubular shape that is less than 360 degrees conformed to a subject's body portion. The acoustic coupling medium is shown in FIG. 5F to be attached to the body housing 101 of an acoustic couplant device.


In some embodiments of the acoustic coupling medium, the partial tubular acoustic coupling medium 505F may be structured to include acoustically attenuating regions in one or more portions of the acoustic coupling medium. As shown in FIG. 5G, an acoustic coupling medium 505G includes the hydrogel and two acoustic attenuating regions located at ends of the partial tube coupling shape to provide acoustically attenuating properties to the acoustic coupling medium 505G.


In various embodiments of the disclosed acoustic coupling medium, the hydrogel can include one or more polymerizable materials that polymerize in the presence of water into hydrophilic gels formed from a natural or synthetic network of polymer chains. Examples of such polymerizable materials include, but are not limited to, polymers and polymer derivatives, alginate, agarose, sodium alginate, chitosan, starch, hydroxyethyl starch, dextran, glucan, gelatin, Poly(vinyl alcohol) (PVA), Poly (N-isopropylacrylamide) (NIPAAm), Poly(vinylpyrrolidone) (PVP), Poly(ethylene glycol) (PEG), Poly(acrylic acid) (PAA), acrylate polymers, Polyacrylamide (PAM), Poly(hydroxyethyl acrylate) (PHEA), Poly(2-propenamide), Poly(1-carbamoylethylene), and Poly(hydroxyethyl methacrylate) (PHEMA). In fabrication techniques to produce the hydrogel, the polymerizable materials can be polymerized through several processes, which may involve toxic or non-toxic chemical compounds, ultraviolet light, irradiation, toxic or nontoxic solvents, temperature cycling, and freeze-thaw cycling. In some implementations to produce the hydrogel, polymerization of the hydrogel through freeze-thaw cycling can be performed, due to the absence of potentially toxic compounds.


For example, the hydrogel can include a material structure that allows acoustic signal propagation with an attenuation factor of 1.0 dB/MHz/cm or less, an impedance of 2.0 MRayls or less, and a longitudinal speed of sound of 1700 m/s or less at 20° C. The acoustic coupler 105 is engineered to have a % elongation of 100% or greater, a density ranging from 1.00-1.20 g/cm3, a shear modulus of less than 1 MPa, and melting and freezing points near 70° C. and −5° C., respectively. For example, the hydrogel material can be at least 90% water and have a pH of −7.0.


In a some embodiments of the acoustic coupling medium, the hydrogel can primarily include water or equivalent solvent and the polymer Poly(vinyl alcohol) (PVA) through the example polymerization process of freeze-thaw cycling, which is a biocompatible polymer and a biocompatible polymerization process for the polymer. The addition of other components, e.g., such as solvents (such as ethyl alcohol or dimethyl sulfoxide) and/or other polymers (such as alginate or gelatin), to this example PVA hydrogel may be employed, as such additional components can be used to improve mechanical or acoustic properties. For example, the addition of one or more bacteriostatic chemicals with sufficient concentration and compatibility with the hydrogel integrity can maintain sterility of the hydrogel during storage and use. Notwithstanding other mechanically, acoustically, and biologically equivalent formulations, the utility of a hydrogel for its acoustic properties due to its high water content, its high tensile strength, and its elasticity is an advantageous feature of the disclosed acoustic coupling medium. The sound speed and acoustic attenuation of the hydrogel may be controlled by varying polymer concentration, water concentration, additional solvent concentration, degree of polymerization, method of polymerization, and inclusion of additional materials such as scattering and/or acoustically absorbing materials.


In one embodiment, for example, the hydrogel includes PVA in a weight ratio of 1-10% and H2O in a weight ratio of 90-99%. The hydrogel is cross-linked through application of 1-10 controlled freeze-thaw cycles cycling in the range of −40° C. to 70° C.


In another embodiment, for example, the hydrogel includes PVA in a weight ratio of 1-10%, DMSO in a weight ratio of 1-10%, and H2O in a weight ratio of 80-98%. The hydrogel is cross-linked through application of 1-10 controlled freeze-thaw cycles cycling in the range of −40° C. to 70° C.


In another embodiment, for example, the hydrogel includes PVA in a weight ratio of 4-10%, PVP in a weight ratio of 1-5%, DMSO in a weight ratio of 1-10%, and H2O in a weight ratio of 75-94%. The hydrogel is cross-linked through application of 1-10 controlled freeze-thaw cycles cycling in the range of −40° C. to 70° C.


In another embodiment, for example, the hydrogel includes PVA in a weight ratio of 4-10%, PVP in a weight ratio of 1-5%, polyethylene glycol in a weight ratio of 1-5%, and H2O in a weight ratio of 80-94%. The hydrogel is cross-linked through application of 1-10 controlled freeze-thaw cycles cycling in the range of −40° C. to 70° C.


In another embodiment, for example, the hydrogel includes PVA in a weight ratio of 4-10%, PVP in a weight ratio of 1-5%, sodium tetraborate in a weight ratio of 1-5%, and H2O in a weight ratio of 80-94%. The borate ions react with hydroxyl groups to cross-link the polymer. The mixture is maintained at a constant temperature during cross-linking.



FIG. 6 shows three dimensional schematic diagrams of an exemplary acoustic coupling medium 505 formed in various shapes, sizes, and configurations. In one example, an acoustic coupling medium 505A′ is configured to have a shape similar to a half cylinder with a 180° curvature, and diameter and depth designed to an initial size, and which are variable to conform to a particular receiving body. In this example, the acoustic coupling medium 505A′ can be configured to have a volume of 3.15 L, which is retained in any shape to which the acoustic coupling medium 505A′ is conformed. In another example, an acoustic coupling medium 105B′ is configured to have a cylindrical shape with a diameter and depth designed to an initial size, and which are variable to conform to a particular receiving body. In this example, the acoustic coupling medium 105B′ can be configured to have a volume of 5.75 L. In other examples, acoustic coupling mediums 505C′, 505D′, 105E′, and 505F′ are configured to have a half-cylinder shape similar to a half donut with a 180° curvature and initial outer diameter and depth designed to an initial size, in which the initial inner diameter of the acoustic coupling mediums 505C′, 505D′, 105E′, and 505F′ is designed to differing sizes (e.g., 40, 80, 120, and 160 mm, respectively), and which the sizes are variable to conform to a particular receiving body, e.g., such as surround the subject's arm, leg, neck, etc. In these examples, the acoustic coupling mediums 505C′, 505D′, 105E′, and 505F′ can be configured to have a volume of 3.0 L, 2.75 L, 2.3 L, and 1.7 L, respectively.



FIGS. 7A-7C show schematic diagrams of exemplary embodiments of the acoustic coupling medium 505D and 505A, featuring three dimensional, front, and side views. As shown in FIG. 7A, the acoustic coupling medium 505D includes the hydrogel configured in a tubular curved shape, which may be wrapped around the secondary medium of the subject and secured by attachment of the attachment component on each end of the hydrogel. The left drawing of FIG. 7A shows a three dimensional schematic view of the hydrogel and the attachment component of the acoustic coupling medium 505D presently detached, and the right drawing of FIG. 7A shows a transparent three dimensional schematic view of the hydrogel secured in the tubular configuration by attachment of the attachment component. In the examples shown in FIG. 7A, the attachment component is structured to include a curved base portion that is sized to the initial size of the depth of the hydrogel and having the same arc curvature as the hydrogel in the tubular configuration. The attachment component is structured to include one or more sets of opposing protrusion structures on the inside surface of the base portion capable of penetrating into the hydrogel to secure the hydrogel in the tubular shape. FIG. 7B shows a transparent front view and a transparent side view of the acoustic coupling medium 505D with the attachment component secured to the hydrogel.



FIG. 7C shows the acoustic coupling medium 505A including the hydrogel configured in a 360° tubular curved shape. The left drawing shows a three dimensional schematic view of the acoustic coupling medium 505A, the center drawing shows a front view of the acoustic coupling medium 505A, and the right drawing shows a side view of the acoustic coupling medium 505A. As depicted in the drawings of FIG. 7C, in this example, the acoustic coupling medium 505A includes a beveled edge at the interface between the outer circular plane surfaces and the outer curved surface, as well as a beveled edge between the outer circular plane surfaces and the inner curved surface. For example, the beveled edge may provide easier and secure loading and unloading of the coupling medium 505A in and out of a bracket or other holder of an acoustic couplant device.



FIG. 8 illustrates a set of operations that can be carried out to produce acoustic waveforms using an acoustic impedance matched couplant in accordance with an exemplary embodiment. At 802, in one or more waveform synthesizers, one or more composite waveforms are synthesized to be transmitted toward a target. A composite waveform is formed of a plurality of individual orthogonal coded waveforms that are mutually orthogonal to each other and correspond to different frequency bands such that each of the individual orthogonal coded waveforms includes a unique frequency with a corresponding phase. At 804, one or more composite acoustic waveforms are transmitted, from one or more transmitting positions relative to the target using an array of transducing elements of an acoustic signal transmission couplant. The one or more composite acoustic waveforms include a plurality of acoustic waveforms, and the transmitting includes selecting one or more of the transducing elements of the array to transduce the plurality of individual orthogonal coded waveforms of the respective one or more composite waveforms into the plurality of corresponding acoustic waveforms of the respective one or more composite acoustic waveforms. At 806, at one or more receiving positions relative to the target, returned acoustic waveforms are received that are returned from at least part of the target corresponding to the transmitted acoustic waveforms. Reception of the returned acoustic waveforms includes selecting at least some of the transducing elements of the array to receive the returned acoustic waveforms. When conducting the above operations, the transmitting positions and the receiving positions each include (i) spatial positions of the array of transducer elements relative to the target and/or (ii) beam phase center positions of the array. Further, the acoustic signal transmission couplant includes an acoustic coupling component including a hydrogel material operable to conduct the acoustic waveforms between the transducer elements and a receiving medium in contact with the acoustic coupling component. The acoustic coupling component is capable of conforming to the receiving medium and the transducer element such that there is an acoustic impedance matching between the receiving medium and the transducer element. The transmitted acoustic waveforms and the returned acoustic waveforms produce an enlarged effective aperture.


Implementations of the subject matter and the functional operations described in this patent document can be implemented in various systems, digital electronic circuitry, or in computer software, firmware, or hardware, including the structures disclosed in this specification and their structural equivalents, or in combinations of one or more of them. Implementations of the subject matter described in this specification can be implemented as one or more computer program products, i.e., one or more modules of computer program instructions encoded on a tangible and non-transitory computer readable medium for execution by, or to control the operation of, data processing apparatus. The computer readable medium can be a machine-readable storage device, a machine-readable storage substrate, a memory device, a composition of matter effecting a machine-readable propagated signal, or a combination of one or more of them. The term “data processing apparatus” encompasses all apparatus, devices, and machines for processing data, including by way of example a programmable processor, a computer, or multiple processors or computers. The apparatus can include, in addition to hardware, code that creates an execution environment for the computer program in question, e.g., code that constitutes processor firmware, a protocol stack, a database management system, an operating system, or a combination of one or more of them.


A computer program (also known as a program, software, software application, script, or code) can be written in any form of programming language, including compiled or interpreted languages, and it can be deployed in any form, including as a stand-alone program or as a module, component, subroutine, or other unit suitable for use in a computing environment. A computer program does not necessarily correspond to a file in a file system. A program can be stored in a portion of a file that holds other programs or data (e.g., one or more scripts stored in a markup language document), in a single file dedicated to the program in question, or in multiple coordinated files (e.g., files that store one or more modules, sub programs, or portions of code). A computer program can be deployed to be executed on one computer or on multiple computers that are located at one site or distributed across multiple sites and interconnected by a communication network.


The processes and logic flows described in this specification can be performed by one or more programmable processors executing one or more computer programs to perform functions by operating on input data and generating output. The processes and logic flows can also be performed by, and apparatus can also be implemented as, special purpose logic circuitry, e.g., an FPGA (field programmable gate array) or an ASIC (application specific integrated circuit).


Processors suitable for the execution of a computer program include, by way of example, both general and special purpose microprocessors, and any one or more processors of any kind of digital computer. Generally, a processor will receive instructions and data from a read only memory or a random access memory or both. The essential elements of a computer are a processor for performing instructions and one or more memory devices for storing instructions and data. Generally, a computer will also include, or be operatively coupled to receive data from or transfer data to, or both, one or more mass storage devices for storing data, e.g., magnetic, magneto optical disks, or optical disks. However, a computer need not have such devices. Computer readable media suitable for storing computer program instructions and data include all forms of nonvolatile memory, media and memory devices, including by way of example semiconductor memory devices, e.g., EPROM, EEPROM, and flash memory devices. The processor and the memory can be supplemented by, or incorporated in, special purpose logic circuitry.


While this patent document contain many specifics, these should not be construed as limitations on the scope of any invention or of what may be claimed, but rather as descriptions of features that may be specific to particular embodiments of particular inventions. Certain features that are described in this patent document in the context of separate embodiments can also be implemented in combination in a single embodiment. Conversely, various features that are described in the context of a single embodiment can also be implemented in multiple embodiments separately or in any suitable subcombination. Moreover, although features may be described above as acting in certain combinations and even initially claimed as such, one or more features from a claimed combination can in some cases be excised from the combination, and the claimed combination may be directed to a subcombination or variation of a subcombination.


Similarly, while operations are depicted in the drawings in a particular order, this should not be understood as requiring that such operations be performed in the particular order shown or in sequential order, or that all illustrated operations be performed, to achieve desirable results. Moreover, the separation of various system components in the embodiments described in this patent document should not be understood as requiring such separation in all embodiments.


Only a few implementations and examples are described and other implementations, enhancements and variations can be made based on what is described and illustrated in this patent document.

Claims
  • 1. A method for tomographic ultrasound imaging using an acoustic coupling article, the method comprising: transmitting, from an array of acoustic transducer elements, an acoustic waveform at a target in a receiving body through an acoustic coupling article that is physically and acoustically coupled to (i) each of the acoustic transducer elements of the array and (ii) the receiving body,wherein the acoustic coupling article comprises: a semi-rigid material including a flexible, continuous pad and able to conform to both a surface of the receiving body and to the array of acoustic transducer elements, such that the semi-rigid material is operable to propagate acoustic signals between the acoustic transducer elements and a receiving medium of the receiving body, andat least one bracket component to secure and conform the semi-rigid material to the array of acoustic transducer elements;receiving one or more returned acoustic waveforms that are returned from at least part of the target corresponding to the transmitted acoustic waveform, wherein the receiving includes selecting at least one of the acoustic transducer elements of the array to receive the one or more returned acoustic waveforms; andproducing a tomographic image of the at least part of the target based on the one or more returned acoustic waveforms,wherein the at least one bracket component includes an arch component to secure the semi-rigid material to interface each acoustic transducer element of the transducer elements of the array.
  • 2. The method of claim 1, wherein the at least one bracket component and the semi-rigid material are coupled by one or more of: the at least one bracket component is at least partially embedded within the semi-rigid material;the at least one bracket component includes one or more clips, one or more notches, or a combination thereof to enable attachment of the semi-rigid material to the at least one bracket component; orthe semi-rigid material includes an adhesive region of the flexible, continuous pad to promote adhesion to the at least one bracket component.
  • 3. The method of claim 1, wherein the at least one bracket component is removably attachable to a housing body that houses the array of acoustic transducer elements.
  • 4. The method of claim 1, further comprising: synthesizing a plurality of individual coded waveforms that correspond to different frequency bands, such that each of the individual coded waveforms includes a unique frequency with respect to another of the individual coded waveforms; andgenerating a composite waveform from at least two or more of the plurality of individual coded waveforms,wherein the transmitted acoustic waveform corresponds to the generated composite waveform.
  • 5. The method of claim 1, wherein the transmitting the acoustic waveform at the target includes: transmitting, from one or more transmitting positions along the array of transducer elements relative to the target, the acoustic waveform.
  • 6. The method of claim 5, wherein the receiving the one or more returned acoustic waveforms from the at least part of the target includes selecting at least one of the transducer elements of the array to receive the one or more returned acoustic waveforms from one or more receiving positions along the array of transducer elements relative to the target, wherein the transmitted acoustic waveform and the received one or more returned acoustic waveforms produce an enlarged effective aperture.
  • 7. The method of claim 6, wherein one or both of the one or more transmitting positions and the one or more the receiving positions include (i) spatial positions of the array of transducer elements relative to the target and/or (ii) beam phase center positions of the array of transducer elements.
  • 8. The method of claim 1, wherein the semi-rigid material of the acoustic coupling article has a thickness in a range of 1 cm to 12 cm.
  • 9. The method of claim 1, wherein the acoustic coupling article is operable to provide an acoustic impedance matching of 2.0 MRayls or less between the receiving medium and the acoustic transducer elements.
  • 10. The method of claim 1, wherein the acoustic coupling article is operable to propagate the acoustic signals with an attenuation factor of 1.0 dB/MHz-cm or less.
  • 11. The method of claim 1, wherein the acoustic coupling article is operable to propagate the acoustic signals with a longitudinal speed of sound at 1700 m/s or less at 20° C.
  • 12. The method of claim 1, wherein the semi-rigid material of the acoustic coupling article includes at least one of a shear modulus of 1 MPa or a density ranging from 1.00-1.20 g/cm3.
  • 13. The method of claim 1, wherein the semi-rigid material of the acoustic coupling article is operable to propagate the acoustic signals while undergoing an elongation of the acoustic coupling article of 100% or greater.
  • 14. The method of claim 1, wherein the semi-rigid material of the acoustic coupling article includes one or more polymerizable materials that form a network structured to entrap an aqueous fluid inside.
  • 15. The method of claim 14, wherein the one or more polymerizable materials include one or more of alginate, agarose, sodium alginate, chitosan, starch, hydroxyethyl starch, dextran, glucan, gelatin, Poly(vinyl alcohol) (PVA), Poly (N-isopropylacrylamide) (NIPAAm), Poly(vinylpyrrolidone) (PVP), Poly(ethylene glycol) (PEG), Poly(acrylic acid) (PAA), acrylate polymers, Polyacrylamide (PAM), Poly(hydroxyethyl acrylate) (PHEA), Poly(2-propenamide), Poly(1-carbamoylethylene), or Poly(hydroxyethyl methacrylate) (PHEMA).
  • 16. The method of claim 14, wherein the aqueous fluid includes water.
  • 17. The method of claim 14, wherein the semi-rigid material of the acoustic coupling article includes an acoustic attenuation region to scatter or absorb the acoustic signals in the acoustic attenuation region, wherein the acoustic attenuation region includes one or more of higher density polymers than the one or more polymerizable materials that form the network, a scattering material, microbubbles, microballoons, a plastic material, a rubber material, or an absorptive material.
  • 18. The method of claim 1, comprising: coupling the acoustic coupling article to the receiving body such that the semi-rigid material conforms to the surface of the receiving body in complete contact to the surface without pockets of air or voids formed between the acoustic coupling article and the receiving body.
  • 19. The method of claim 1, wherein the receiving body includes an anatomical structure of a living subject including an abdomen, a thorax, a neck including a throat, an arm, a leg, a knee joint, a hip joint, an ankle joint, an elbow joint, a shoulder joint, a wrist joint, a breast, a genital, or a head including a cranium.
CROSS REFERENCE TO RELATED APPLICATIONS

This patent document is a continuation of and claims priority to U.S. patent application Ser. No. 16/294,847, filed on Mar. 6, 2019, which is a continuation of and claims priority to U.S. patent application Ser. No. 15/053,502, filed on Feb. 25, 2016, now U.S. Pat. No. 10,743,838, which claims the benefit of priority of U.S. Provisional Patent Application No. 62/120,839, filed on Feb. 25, 2015, and U.S. Provisional Patent Application No. 62/174,999, filed on Jun. 12, 2015. The entire contents of the before-mentioned patent applications are incorporated by reference as part of the disclosure of this document.

US Referenced Citations (259)
Number Name Date Kind
4105018 Greenleaf et al. Aug 1978 A
4110755 Zottl Aug 1978 A
4159462 Rocha et al. Jun 1979 A
4277367 Madsen et al. Jul 1981 A
4437468 Sorenson Mar 1984 A
4463608 Takeuchi et al. Aug 1984 A
4620546 Aida et al. Nov 1986 A
4821206 Arora Apr 1989 A
4830015 Okazaki May 1989 A
4888746 Wurster et al. Dec 1989 A
5005418 Anderson Apr 1991 A
5039774 Shikinami et al. Aug 1991 A
5181513 Touboul et al. Jan 1993 A
5241964 McQuilkin Sep 1993 A
5269309 Fort et al. Dec 1993 A
5284143 Rattner Feb 1994 A
5329944 Fabian et al. Jul 1994 A
5394877 Orr Mar 1995 A
5417218 Spivey et al. May 1995 A
5445144 Wodicka et al. Aug 1995 A
5465722 Fort et al. Nov 1995 A
5522878 Montecalvo Jun 1996 A
5533510 Koch, III et al. Jul 1996 A
5608690 Hossack et al. Mar 1997 A
5623928 Wright et al. Apr 1997 A
5682886 Delp et al. Nov 1997 A
5753095 Alpenfels et al. May 1998 A
5793701 Wright et al. Aug 1998 A
5800356 Criton et al. Sep 1998 A
5803089 Ferre et al. Sep 1998 A
5806518 Mittelstadt Sep 1998 A
5829444 Ferre et al. Nov 1998 A
5868676 McCabe et al. Feb 1999 A
5873830 Hossack et al. Feb 1999 A
5882557 Hayakawa et al. Mar 1999 A
5902244 Kobayashi et al. May 1999 A
5913823 Hedberg et al. Jun 1999 A
5967980 Ferre et al. Oct 1999 A
6016285 Wright et al. Jan 2000 A
6039694 Larson Mar 2000 A
6045507 Muzilla et al. Apr 2000 A
6050945 Peterson et al. Apr 2000 A
6083164 Oppelt et al. Jul 2000 A
6106464 Bass et al. Aug 2000 A
6107365 Bertozzi et al. Aug 2000 A
6110114 Nock et al. Aug 2000 A
6113544 Mo Sep 2000 A
6123669 Kanda Sep 2000 A
6132375 Napolitano Oct 2000 A
6157592 Kriz et al. Dec 2000 A
6205411 DiGioia, III et al. Mar 2001 B1
6231834 Unger et al. May 2001 B1
6241676 Savord Jun 2001 B1
6322567 Mittelstadt et al. Nov 2001 B1
6338765 Statnikov Jan 2002 B1
6340363 Bolger et al. Jan 2002 B1
6341231 Ferre et al. Jan 2002 B1
6402707 Ernst Jun 2002 B1
6425865 Salcudean et al. Jul 2002 B1
6436045 Rafter et al. Aug 2002 B1
6445943 Ferre et al. Sep 2002 B1
6508766 Sato et al. Jan 2003 B2
6537216 Shifrin Mar 2003 B1
6583392 Hershey et al. Jun 2003 B2
6585648 Robinson Jul 2003 B1
6620101 Azzam et al. Sep 2003 B2
6626916 Yeung et al. Sep 2003 B1
6652461 Levkovitz Nov 2003 B1
6687531 Ferre et al. Feb 2004 B1
6725082 Sati et al. Apr 2004 B2
6736780 Song et al. May 2004 B2
6757582 Brisson et al. Jun 2004 B2
6785571 Glossop Aug 2004 B2
6786097 Song et al. Sep 2004 B2
6796988 Melkent et al. Sep 2004 B2
6808494 Shifrin Oct 2004 B2
6843957 Statnikov Jan 2005 B2
6918877 Hossack et al. Jul 2005 B2
6934575 Ferre et al. Aug 2005 B2
6939300 Petersen et al. Sep 2005 B2
6960173 Babaev Nov 2005 B2
7004906 Guracar et al. Feb 2006 B1
7066886 Song et al. Jun 2006 B2
7070565 Vaezy Jul 2006 B2
7207939 Husher Apr 2007 B2
7226456 O'Neil et al. Jun 2007 B2
7291119 de Guise et al. Nov 2007 B1
7344609 Statnikov Mar 2008 B2
7395181 Foxlin Jul 2008 B2
7473250 Makin et al. Jan 2009 B2
7532201 Quistgaard et al. May 2009 B2
7542790 Jensen et al. Jun 2009 B2
7566304 Nakamura et al. Jul 2009 B2
7601966 Ben-Haim Oct 2009 B2
7678049 Tsoref et al. Mar 2010 B2
7719515 Fujiwara et al. May 2010 B2
7719689 Lee et al. May 2010 B2
7728487 Adachi et al. Jun 2010 B2
7763035 Melkent et al. Jul 2010 B2
7798585 Oguri Sep 2010 B2
7806823 Sakai et al. Oct 2010 B2
7826889 David et al. Nov 2010 B2
7835778 Foley et al. Nov 2010 B2
7835784 Mire et al. Nov 2010 B2
7837625 Abe Nov 2010 B2
RE42194 Foley et al. Mar 2011 E
7905836 Dan Mar 2011 B2
7917317 McKeon Mar 2011 B2
7938777 Amiot et al. May 2011 B2
7938778 Sakai May 2011 B2
7982362 Adachi et al. Jul 2011 B2
8002705 Napolitano et al. Aug 2011 B1
8038616 Angelsen et al. Oct 2011 B2
8043220 Okada et al. Oct 2011 B2
8103461 Glaser et al. Jan 2012 B2
8105339 Melkent et al. Jan 2012 B2
8126533 Lavallee Feb 2012 B2
8147409 Shifrin Apr 2012 B2
8152726 Amiot et al. Apr 2012 B2
8165658 Waynik et al. Apr 2012 B2
8241217 Chiang et al. Aug 2012 B2
8251908 Vortman et al. Aug 2012 B2
8253578 Watabe et al. Aug 2012 B2
8311611 Csavoy et al. Nov 2012 B2
8323200 Kunita Dec 2012 B2
8372070 Tanaka et al. Feb 2013 B2
8374674 Gertner Feb 2013 B2
8409099 Vitek Apr 2013 B2
8409103 Grunwald et al. Apr 2013 B2
8444564 Mahfouz et al. May 2013 B2
8447388 Igarashi May 2013 B2
8491476 Iwama et al. Jul 2013 B2
8556834 Gertner Oct 2013 B2
8565860 Kimchy et al. Oct 2013 B2
8626267 Lavallee Jan 2014 B2
8675939 Moctezuma De La Barrera Mar 2014 B2
8771188 Schers et al. Jul 2014 B2
8774900 Buly et al. Jul 2014 B2
8814810 Roche et al. Aug 2014 B2
8864686 Roche et al. Oct 2014 B2
8880152 Lavallee Nov 2014 B2
8909325 Kimchy et al. Dec 2014 B2
8939909 Wegner Jan 2015 B2
8986609 Rau et al. Mar 2015 B2
9060794 Kang et al. Jun 2015 B2
9101394 Arata et al. Aug 2015 B2
9174065 Gertner Nov 2015 B2
9196046 Meyer Nov 2015 B2
9220571 Lavallee Dec 2015 B2
9244169 Fan et al. Jan 2016 B2
9248001 Colombet et al. Feb 2016 B2
9352171 Gertner May 2016 B2
9387276 Sun et al. Jul 2016 B2
9420999 Wegner Aug 2016 B2
9572548 Moctezuma de la Barrera Feb 2017 B2
9597058 Kanayama et al. Mar 2017 B2
9844359 Wegner Dec 2017 B2
9872667 Wegner Jan 2018 B2
9878506 Zhao et al. Jan 2018 B2
10085722 Wegner Oct 2018 B2
10321889 Wegner Jun 2019 B2
10336896 Zheng et al. Jul 2019 B2
10426429 Kruse et al. Oct 2019 B2
10743838 Freiburg et al. Aug 2020 B2
10975205 Illeperuma et al. Apr 2021 B2
10993699 Wegner May 2021 B2
11096661 Wegner Aug 2021 B2
11154274 Wegner Oct 2021 B2
11191521 Freiburg et al. Dec 2021 B2
11607192 Wegner Mar 2023 B2
20020068871 Mendlein et al. Jun 2002 A1
20020099290 Haddad Jul 2002 A1
20020122536 Kerrien et al. Sep 2002 A1
20020188198 Hong Dec 2002 A1
20020188229 Ryaby et al. Dec 2002 A1
20030036702 Davidsen Feb 2003 A1
20030125628 Song et al. Jul 2003 A1
20030233045 Vaezy Dec 2003 A1
20040066708 Ogawa Apr 2004 A1
20040236223 Barnes et al. Nov 2004 A1
20050101861 Satoh May 2005 A1
20050101867 Johnson et al. May 2005 A1
20050113698 Kristoffersen May 2005 A1
20050154302 Sela et al. Jul 2005 A1
20050203399 Vaezy Sep 2005 A1
20050215893 Barnes et al. Sep 2005 A1
20060004290 Smith et al. Jan 2006 A1
20060119223 Ossmann Jun 2006 A1
20060173305 Asafusa et al. Aug 2006 A1
20070066897 Sekins et al. Mar 2007 A1
20070156050 Barnes et al. Jul 2007 A1
20070226976 Zipparo et al. Oct 2007 A1
20070239001 Mehi et al. Oct 2007 A1
20070239002 Alam Oct 2007 A1
20070265690 Lichtenstein et al. Nov 2007 A1
20070276238 Sudol Nov 2007 A1
20080051655 Sato Feb 2008 A1
20080110263 Klessel et al. May 2008 A1
20080119737 Urbano et al. May 2008 A1
20080200810 Buchalter Aug 2008 A1
20080208055 Bertram et al. Aug 2008 A1
20080262347 Batchelder et al. Oct 2008 A1
20080281202 Fraser et al. Nov 2008 A1
20080281237 Slayton Nov 2008 A1
20090043206 Towfiq et al. Feb 2009 A1
20090093737 Chomas Apr 2009 A1
20090124871 Arshak et al. May 2009 A1
20090306497 Manzke et al. Dec 2009 A1
20100029789 Chen Feb 2010 A1
20100179425 Zadicario Jul 2010 A1
20100204577 Sekins et al. Aug 2010 A1
20100268072 Hall et al. Oct 2010 A1
20100274139 Fukukita et al. Oct 2010 A1
20100280379 Satoh Nov 2010 A1
20100286518 Lee et al. Nov 2010 A1
20100286527 Cannon Nov 2010 A1
20110060226 Yen et al. Mar 2011 A1
20110092862 Chivers Apr 2011 A1
20110264012 Lautzenhiser et al. Oct 2011 A1
20120029345 Mahfouz et al. Feb 2012 A1
20120238875 Savitsky et al. Sep 2012 A1
20120253071 Rau et al. Oct 2012 A1
20120281507 Rikoski Nov 2012 A1
20130060121 Patwardhan et al. Mar 2013 A1
20130102875 Dogra et al. Apr 2013 A1
20130123635 Wegner May 2013 A1
20130144135 Mahfouz et al. Jun 2013 A1
20130144166 Specht et al. Jun 2013 A1
20130150863 Baumgartner Jun 2013 A1
20130165005 Berard-Andersen et al. Jun 2013 A1
20130218013 Barthe et al. Aug 2013 A1
20140163377 Kang et al. Jun 2014 A1
20140180116 Lindekugel et al. Jun 2014 A1
20140353248 Kuraray Dec 2014 A1
20150018682 Schers et al. Jan 2015 A1
20150038613 Sun et al. Feb 2015 A1
20150088040 Barthe et al. Mar 2015 A1
20150133788 Mauldin, Jr. et al. May 2015 A1
20150164467 Suetoshi et al. Jun 2015 A1
20150182191 Caluser et al. Jul 2015 A1
20150274805 Annabi et al. Oct 2015 A1
20150313572 Gerbaulet Nov 2015 A1
20160000409 Bruder et al. Jan 2016 A1
20160083574 Zheng et al. Mar 2016 A1
20160100821 Eggers et al. Apr 2016 A1
20160176128 Zhao Jun 2016 A1
20160270763 Hayes et al. Sep 2016 A1
20160354520 Sun et al. Dec 2016 A1
20170368333 Loudin et al. Dec 2017 A1
20180126677 Zhao et al. May 2018 A1
20180240366 Felsinger et al. Aug 2018 A1
20180244858 Illeperuma et al. Aug 2018 A1
20190070826 Zhao et al. Mar 2019 A1
20200029931 Kruse et al. Jan 2020 A1
20200138409 Lindekugel et al. May 2020 A1
20210353259 Wegner Nov 2021 A1
20210361259 Wegner Nov 2021 A1
20220106424 Staebler Apr 2022 A1
20220134608 Staebler May 2022 A1
Foreign Referenced Citations (56)
Number Date Country
2427186 May 2001 CA
2852801 May 2013 CA
100354651 Dec 2007 CN
101325913 Dec 2008 CN
102258399 Nov 2012 CN
104169739 Nov 2014 CN
952461 Oct 1999 EP
1707124 Apr 2006 EP
1795917 Jun 2007 EP
1854406 Nov 2007 EP
1955668 Aug 2008 EP
2033579 Mar 2009 EP
2379392 Mar 2003 GB
2472066 Jan 2011 GB
232148 Jul 2019 IL
55051351 Apr 1980 JP
58195550 Nov 1983 JP
60048736 Mar 1985 JP
62117535 May 1987 JP
H03114453 May 1991 JP
8038473 Feb 1996 JP
2000041980 Feb 2000 JP
2000166922 Jun 2000 JP
2000287988 Oct 2000 JP
2001515924 Sep 2001 JP
2003190157 Jul 2003 JP
2004147852 May 2004 JP
2005152608 Jun 2005 JP
2005527336 Sep 2005 JP
2007152127 Jun 2007 JP
2010082425 Apr 2010 JP
2011062531 Mar 2011 JP
2011177461 Sep 2011 JP
2012002586 Jan 2012 JP
2013056156 Mar 2013 JP
2013520235 Jun 2013 JP
2013539715 Oct 2013 JP
2014533154 Dec 2014 JP
2014103512 Jan 2017 JP
2002024094 Mar 2002 WO
2007023477 Mar 2007 WO
2007069156 Jun 2007 WO
2009009064 Jan 2009 WO
2009020617 Feb 2009 WO
2009063421 May 2009 WO
2013066821 May 2013 WO
2013103956 Jul 2013 WO
2014128593 Aug 2014 WO
2014150780 Sep 2014 WO
2014150961 Sep 2014 WO
2014186904 Nov 2014 WO
2015038554 Mar 2015 WO
2016044830 Mar 2016 WO
2016138257 Sep 2016 WO
2016149427 Sep 2016 WO
2017164902 Sep 2017 WO
Non-Patent Literature Citations (94)
Entry
Walker, Ezekiel, et al. “Anomalous temperature dependence of speed of sound of bulk poly (N-isopropylacrylamide) hydrogels near the phase transition.” Ultrasonics 54.5 (2014): 1337-1340. (Year: 2014).
Office Action dated Jul. 12, 2022 in Chinese Patent Application No. 202080021490.7, with English translation, 18 pages.
Office Action dated Jul. 28, 2022 in Korean Patent Application No. 2017-7027091, machine translation obtained from USPTO Global Dossier, 28 pages.
Sun, J.Y. et al., “Highly stretchable and tough hydrogels,” Nature, vol. 489, Sep. 6, 2012, 21 pages.
Callow, H.J., “Signal Processing for Synthetic Aperture Sonar Image Enhancement,” Thesis for Ph.D. in Electrical and Electronic Engineering at the University of Canterbury, Christchurch, New Zealand, 273 pages, April 2003.
Cao, Z. et al., “Fabrication and properties of thermosensitive organic/inorganic hybrid hydrogel thin films,” Langmuir, American Chemical Society, vol. 24, No. 10, May 20, 2008, pp. 5543-5551.
Chiao, R., “Coded Excitation for Diagnostic Ultrasound: A System Developer's Perspective,” IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, 52(2):160-170, Feb. 2005.
Choe, J.W., et al., “Volumetric real-time imaging using a CMUT ring array,” IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, 59(6):1201-1211, Jun. 2012
Demi, L., et al., “In Vitro and In Vivo Tissue Harmonic Images Obtained With Parallel Transmit Beamforming by Means of Orthogonal Frequency Division Multiplexing,” IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, 62(1):230-235, Jan. 2015.
European Search Report dated Apr. 19, 2017 for European Application No. 14844538.0, filed on Sep. 9, 2014 (10 pages).
European Search Report dated Feb. 1, 2019 for European Application No. 16756353.5, filed on Feb. 25, 2016 (14 pages).
European Search Report dated Jun. 29, 2015 for European Application No. 12845256.2, filed on Oct. 29, 2012 (8 pages).
European Search Report dated Nov. 9, 2018 for European Application No. 16765701.4, filed on Mar. 16, 2016 (6 pages).
Exam Report dated November 1, 2019 for Australian Application No. 2016233279, filed on Mar. 16, 2016 (3 pages).
Exam Report dated Oct. 18, 2019 for Australian Application No. 2016222637, filed on Feb. 25, 2016 (3 pages).
Exam Report dated Feb. 26, 2019 for Singapore Application No. 11201706953Y, filed on Feb. 25, 2016 (6 pages).
Examination Report dated Dec. 20, 2019 for Europe Patent Application No. 14844538.0, filed on Sep. 9, 2014 (7 pages).
Examination Report dated Jul. 19, 2021 for European Application No. 12845256.2, filed on Oct. 29, 2012 (8 pages).
Examination Report dated Jul. 26, 2018 for Canada Patent Application No. 2,852,801, filed on Oct. 29, 2012, 4 pages.
Examination Report dated Jun. 22, 2020 for Australian Application No. 2016334258, 4 pages.
Examination Report dated Mar. 16, 2018 for European Application No. 12845256.2, filed on Oct. 29, 2012 (8 pages).
Extended European Search Report dated Feb. 15, 2019 for European Application No. 16765701.4, filed on Mar. 16, 2016 (14 pages).
Extended European Search Report dated Jul. 2, 2019 for European Application No. 16756353.5, filed on Feb. 25, 2016 (14 pages).
Extended European Search Report dated Jun. 18, 2019 for European Application No. 16854507.7, filed on Oct. 7, 2016 (11 pages).
Extended Search Report dated Jun. 18, 2019 for European Application No. 16854507.7, filed on Oct. 7, 2016 (11 pages).
First Examination Report dated Apr. 12, 2016 for Australian Patent Application No. 2012332817, filed on Oct. 29, 2012, 3 pages.
First Examination Report dated Nov. 21, 2018 for Australian Patent Application No. 2018203785, filed on Oct. 29, 2012, 2 pages.
First Office Action dated Aug. 14, 2020 for Chinese Patent Application No. 201680071645.1, with English translation, 35 pages.
Hunter, A.J., et al., “A Comparison of Fast Factorised Back-Projection and Wavenumber Algorithms for SAS Image Reconstruction,” Proceedings of the World Congress on Ultrasonics, 4 pages, (2003).
International Search Report and Written Opinion dated Jul. 16, 2020 for International App. PCT/US20/29564 filed Apr. 23, 2020, 11 pages.
International Search Report and Written Opinion dated Dec. 29, 2016 for International Application No. PCT/US2016/056159, filed on Oct. 7, 2016 (7 pages).
International Search Report and Written Opinion dated Jul. 2, 2020 for International Application No. PCT/US2020/021456, filed on Mar. 6, 2020, 16 pages.
International Search Report and Written Opinion dated Jul. 6, 2016 for International Application No. PCT/US2016/019554, filed on Feb. 25, 2016 (12 pages).
International Search Report and Written Opinion dated Mar. 3, 2015 for International Application No. PCT/US2014/054855, filed on Sep. 9, 2014 (11 pages).
International Search Report and Written Opinion dated May 15, 2013 for International Application No. PCT/US2012/062435, filed on Oct. 29, 2012 (9 pages).
International Search Report and Written Opinion dated May 18, 2020 for International Application No. PCT/US20/18123, filed on Feb. 13, 2020 (11 pages).
Ito, T., et al., “Evaluation of Acoustic Imaging System Using Correlation Division in Synthetic Transmit Aperture with Multicarrier Signals,” IEICE Transactions on Fundamentals of Electronics, Communications and Computer Sciences, E94-A(10):1907-1919, Oct. 2011.
Jensen, J.A., et al., “Synthetic Aperture Ultrasound Imaging,” Ultrasonics, 44(Suppl 1):e5- e15, Dec. 2006.
Koch, A., et al., “An Ultrasound Tomography System With Polyvinyl Alcohol (PVA) Moldings for Coupling: In Vivo Results for 3-D Pulse-Echo Imaging of the Female Breast,” IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, 62(2):266-279, Feb. 2015.
Kundur, D., et al., “A Novel Blind Deconvolution Scheme for Image Restoration Using Recursive Filtering,” IEEE Transactions on Signal Processing, 46(2):375-390, Feb. 1998.
Misaridis, T., “Use of Modulated Excitation Signals in Medical Ultrasound. Part I: Basic Concepts and Expected Benefits,” IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, 52(2):177-191, Feb. 2005.
Misaridis, T., “Use of Modulated Excitation Signals in Medical Ultrasound. Part II: Design and Performance for Medical Imaging Applications,” IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, 52(2):192-207, Feb. 2005.
Misaridis, T., “Use of Modulated Excitation Signals in Medical Ultrasound. Part III: High Frame Rate Imaging,” IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, 52(2):208-219, Feb. 2005.
Notification of Defects dated Nov. 22, 2017 for Israel Patent Application No. 232148, filed on Oct. 29, 2012, 4 pages.
O'Donnell, M., “Coded Excitation for Synthetic Aperture Ultrasound Imaging,” IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control, 52(2):171-176, Feb. 2005.
Office Action dated Aug. 30, 2020 for Israel Application No. 264906, filed on Oct. 29, 2012, with English translation, 10 pages.
Office Action dated Jan. 13, 2020 for Chinese Application No. 201680028663.1, filed on Mar. 16, 2016 (17 pages).
Office Action dated Jan. 14, 2020 for Japanese Application No. 2017-563504, filed on Feb. 25, 2016 (14 pages).
Office Action dated Jun. 3, 2021 for Israel Application No. 258533, 7 pages, with English Translation.
Office Action dated Jun. 4, 2019 for Japanese Application No. 2017-187288, filed on Oct. 29, 2012 (3 pages).
Office Action dated Mar. 17, 2020 for Japanese Application No. 2018-145683, filed on Sep. 9, 2014 (4 pages).
Office Action dated Mar. 25, 2020 for Japanese Application No. 2016-542050, filed on Sep. 9, 2014 (4 pages).
Office Action dated Oct. 20, 2020 for Canadian Application No. 2,923,861, 4 pages.
Office Action dated Oct. 29, 2019 for Japanese Application No. 2018-145683, filed on Sep. 9, 2014 (3 pages).
Office Action dated Oct. 29, 2021 in Chinese Patent Application No. 201680071645.1, with English translation, 28 pages.
Office Action dated Oct. 7, 2021 in Israel Patent Application No. 254158, 6 pages, with English translation.
Office Action dated on Dec. 4, 2019 for Chinese Application No. 201680023999.9, filed on Feb. 25, 2016 (23 pages).
Office Action dated Feb. 25, 2020 for Japanese Application No. 2017-549178, filed on Mar. 16, 2016 (8 pages).
Office Action dated Jul. 3, 2018 for Japanese Application No. 2017-187288, filed on Oct. 29, 2012 (6 pages).
Office Action dated Jun. 11, 2019 for Japanese Application No. 2016-542050, filed on Sep. 9, 2014 (15 pages).
Office Action dated Jun. 18, 2019 for Japanese Patent Application No. 2018-145683, filed on Sep. 9, 2014, 12 pages.
Office Action dated Jun. 5, 2018 for Chinese Patent Application No. 201480062224.3, filed on Sep. 9, 2014, 13 pages.
Office Action dated Sep. 13, 2016 for Japanese Application No. 2014-539114, filed on Oct. 29, 2012 (4 pages).
Office Action dated Sep. 19, 2017 for Japanese Application No. 2016-542050, filed on Sep. 9, 2014 (15 pages).
Office Action dated Sep. 2, 2015 for Chinese Application No. 201280065031.4, filed on Oct. 29, 2012 (26 pages).
Office Action dated Sep. 23, 2020 for Israel Application No. 254158, filed Feb. 25, 2016, english translation, 3 pages.
Office Action dated Sep. 23, 2020 in Israel Patent Application No. 254158, 3 pages.
Prokop A F et al., “Polyacrylamide gel as an acoustic coupling medium for focused ultrasound therapy.” Ultrasound in Medicine and Biol, New York, NY, US, vol. 29, No. 9, Sep. 1, 2003, pp. 1351-1358.
Rui Silva, S., et al., “2 Synthetic Aperture Techniques for Sonar Systems,” Advances in Sonar Technology, edited by Sergio Rui Silva, publisher I-Tech Education and Publishing, ISBN 978-3-902613-48-6, pp. 15-42, Feb. 2009.
Second Office Action dated Jul. 14, 2020 for Chinese Patent Application No. 201680023999.9 (41 pages).
Second Office Action dated Jul. 14, 2020 for Chinese Patent Application No. 201680023999.9, filed on Feb. 25, 2016, 41 pages, with English translation.
Second Office Action dated Jul. 20, 2016 for Chinese Patent Application No. 201280065031.4, filed on Oct. 29, 2012 (26 pages).
Second Office Action dated Jun. 1, 2021 for Chinese Patent Application No. 201680071645.1, with English translation, 32 pages.
Singapore Exam Report dated Feb. 26, 2019 for Singapore Application No. 11201706953Y, filed on Feb. 25, 2016 (6 pages).
Singapore Search Report dated Sep. 24, 2018 for Singapore Application No. 11201706953Y, filed on Feb. 25, 2016 (13 pages).
Singapore Written Opinion dated Jul. 10, 2017 for Singapore Application No. 11201601906P, filed on Sep. 9, 2014 (8 pages).
Singapore Written Opinion dated Jun. 21, 2018 for Singapore Application No. 11201707641P, filed on Mar. 16, 2016 (8 pages).
Singapore Written Opinion dated Mar. 11, 2020 for Singapore Application No. 11201707641P, filed on Mar. 16, 2016 (8 pages).
Trots, I. et al., “Synthetic Aperture Method in Ultrasound Imaging,” Chapter 3 of Ultrasound Imaging, edited by Masayuki Tanabe, 2011, pp. 37-56.
Zhu, S., et al., “SAS Autofocus Based on Phase Gradient Autofocus,” IEEE 2011 Fourth International Workshop on Chaos-Fractals Theories and Applications (IWCFTA), pp. 298-301, Oct. 19-22, 2011.
Examination Report dated August 9, 2022 for European Patent Application No. 16854507.7, 8 pages.
European Search Report dated October 26, 2022 in European Patent Application No. 20767211.4, 13 pages.
European Search Report dated Oct. 17, 2022 in European Patent Application No. 20756147.3, 6 pages.
Examination Report dated Dec. 21, 2022 in Canadian Patent Application No. 3,001,315, 4 pages.
Examination Report dated Oct. 4, 2022 in European Patent Application No. 14844538.0, 4 pages.
Extended European Search Report dated Jan. 26, 2023 for European Patent Application No. 20767211.4, 11 pages.
Laferriere et al. “Syntheses of Water-Soluble Polyacrylamide-Containing Sialic Acid.” Methods in Enzymology, vol. 242, 1994, 10 pages.
Low, Z.W. et al., “The role of hydrogen bonding in alginate/poly(acrylamide-co-dimethylacrylamide) and alginate/poly(ethylene glycol) methyl ether methacrylate-based tough hybrid hydrogels.” Royal Society of Chemistry, 2015, 5, 8 pages.
Low, Z.W et al., Supporting Information. “The role of hydrogen bonding in alginate/poly(acrylamide-co-dimethylacrylamide) and alginate/poly(ethylene glycol) methyl ether methacrylate-based tough hybrid hydrogels.” Royal Society of Chemistry, 2015, 5, 5 pages.
Notice of Final Rejection dated Feb. 23, 2023 for Korean Patent Application No. 10-2017-7027091, with English Translation, 13 pages.
Notice of Preliminary Rejection dated Jul. 28, 2022 for Korean Patent Application No. 10-2017-7027091, 22 pages.
Notice of Requisition dated Mar. 10, 2023 in Canadian Patent Application No. 2,977,975, 4 pages.
Notice of Preliminary Rejection dated Jul. 28, 2023 for Korean Patent Application No. 10-2018-7012592, English Translation, 2 pages.
Notice of Reasons for Rejection dated Sep. 26, 2023 in Japanese Patent Application No. 2021-552570, English Translation, 4 pages.
Related Publications (1)
Number Date Country
20220192634 A1 Jun 2022 US
Provisional Applications (2)
Number Date Country
62174999 Jun 2015 US
62120839 Feb 2015 US
Continuations (2)
Number Date Country
Parent 16294847 Mar 2019 US
Child 17542211 US
Parent 15053502 Feb 2016 US
Child 16294847 US