专利摘要:
An embodiment in accordance with the present invention provides a device and method to deliver direct ionic current safely to target neural tissue, while also eliminating interruptions in the output of the device that can result from the non-ideal operation of the valves used to control the current flow in the device. The device includes two valve-operated systems that work in tandem. The first and second current producing systems are configured to be used together in order to eliminate the periodic interruptions in current flow. In use, one system drives current through the target tissue, while the other system closes all of the valves first and then opens its valves in sequence. This intermediate step of closing all of the valves prevents unintended current shunts through either system. The device also includes two conductors to direct the flow of direct current into the target tissue.
公开号:AU2012358886A1
申请号:U2012358886
申请日:2012-12-20
公开日:2014-07-17
发明作者:Charles Coleman Della Santina;Gene Yevgeny Fridman
申请人:Johns Hopkins University;
IPC主号:A61N1-20
专利说明:
WO 2013/096574 PCT/US2012/070860 Artifact Control and Miniaturization of the Safe Direct Current Stimulator for Neural Prostheses GOVERNMENT SUPPORT 5 This invention was made with government support under NIH RO1DC009255 awarded by the National Institute of Health. The government has certain rights in the invention. 10 CROSS REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Patent Application No. 61/577,82 1, filed December 20, 2011, which is incorporated by reference herein, in its entirety. 15 FIELD OF THE INVENTION The present invention relates generally to neural stimulation. More particularly, the present invention relates to a device and method for delivering DC current to target tissue. 20 BACKGROUND OF THE INVENTION While effective in treating some neurological disorders, neural prostheses are limited because they can excite neurons but not efficiently inhibit them. Direct current (DC) applied to a metal electrode in contact with neural tissue can excite or inhibit neural activity; however, DC stimulation is biologically unsafe because it causes electrochemical reactions at 25 the metal electrode-tissue interface. To avoid these safety hazards, neural prostheses generally deliver alternating current (AC) pulses to evoke action potentials. While cochlear and retinal prostheses use AC pulses to encode sensory information by modulating firing rate of the afferent fibers above their spontaneous activity, other neural prosthesis applications have substantial difficulties achieving effective treatment with 30 excitation alone. A prosthesis to assist micturition, for instance, requires both excitation of 1 WO 2013/096574 PCT/US2012/070860 sacral nerves to activate the detrusor muscle and simultaneous inhibition of lumbar nerves to relax the urethral sphincter. For proper balance as well, inner ear vestibular afferent fibers require not only excitation to encode head motion toward the stimulated side of the head, but also inhibition to encode head motion away from it. In restoring normal physiology, 5 therefore, the ability for a neural prosthesis to both inhibit and excite neurons would be useful. Furthermore, several disorders characterized by high neural firing rates such as tinnitus, chronic pain, and epilepsy could be effectively treated by prostheses capable of neural inhibition. Gradual modulation of extracellular potential rather than evoking or inhibiting spikes could further extend the capabilities of neural prostheses to treating 10 disorders such as autism by addressing excitatory vs. inhibitory imbalance, and DC potential support to treat strial hearing loss. At low amplitudes, DC can achieve graded control of neural activity by altering the extracellular electric field near the electrode. By altering the electric field, DC modulates neural firing thresholds, increasing or decreasing the likelihood of spike initiation. At higher 15 DC amplitudes, cathodic current excites neurons, while anodic current inhibits them. DC stimulation that does not produce electrochemical reactions at the electrode-saline interface could enable more versatile treatments of neurological disorders than what is currently possible. A solution to the problem of DC stimulation safety is to direct the DC flow of ions 20 into the target tissue by switching mechanical valves in phase with AC square waves applied to the electrodes, which are immersed in an ionic solution. This approach removes DC from the electrode-saline interface, while maintaining DC ionic current through the tissue. FIG. 1A shows the two potential states of the system. FIG. 1B shows the output of the fully functioning SDCS as the valves operate in synchrony with AC delivered to the electrodes. 25 One important aspect of this device is that it works in a bipolar configuration so that the ions 2 WO 2013/096574 PCT/US2012/070860 flowing into one tube are replenished by the same types of ions flowing out of the other tube thus resulting in net zero ionic change in the tissue between the two tubes. This configuration addresses pH changes that could potentially be harmful to the neural tissue. The fidelity of the DC signal is degraded by periodic interruptions in current flow due 5 to non-ideal behavior of the mechanical valves used in the device, as illustrated in FIG. 1B. The interruptions occur because ionic current bypasses the tissue when the valves are temporarily and simultaneously either open or closed during open-to-close and close-to-open transitions. For example, if B2 and A2 are both closed during a transition, no current will flow through the tissue. The duration of the interruptions depends on the speed of the valve 10 transitions from open-to-close and from close-to-open states. Any interruption in the DC current flow however will cause the undesirable volley of neural activity in the target neurons. It would therefore be advantageous to provide a method to remove the interruptions in the ionic direct current flow. 15 SUMMARY OF THE INVENTION The foregoing needs are met, to a great extent, by the present invention, wherein in one aspect, a device for delivering direct current includes a first set of two electrodes and a second set of two electrodes configured to receive alternating current. The device also includes a first set of valves. The first set of valves includes a first and second pair of valves. 20 The device also includes a second set of valves. The second set of valves includes a third and fourth pair of valves. The first and second sets of valves are configured to be opened and closed and are further configured to switch in phase with the alternating current applied to the first electrode and the second electrode. A tube is filled with conductive material and configured to direct the direct current flow of ions into target tissue. Additionally, the device 3 WO 2013/096574 PCT/US2012/070860 is configured such that the first set of valves is closed when the third and fourth pairs of valves are being opened and the second set of valves is closed when the first and second pairs of valves are being opened. In accordance with another aspect of the present invention, two systems work in 5 tandem. In the arrangement described in the present invention, one system controls the ionic current system output to the tissue, while the second system undergoes valve transitions without affecting the device output. After the valves transition states in the second system, control of the device output switches electronically from the first system to the second thus allowing the first system to switch its valves without affecting the device output. In this way, 10 the smooth ionic current output of the device is maintained independent of the valve transition speed. In accordance with an aspect of the present invention, the conductor takes the form of a tube defining a hollow lumen extending therethrough. The hollow lumen of the tube is filled with a conductive material, and the conductive material is an ionic solution or an ionic 15 hydrogel. The system further includes a housing having multiple layers. Each one of the layers of the housing contains one of the electrodes or the first set of valves and the second set of valves. Layer 1 of the housing contains channels filled with an ionic solution or electrolytic gel to conduct ionic current flow. Layer 2 encloses and protects layer 1 and provides openings through which the channels in layer 1 can be connected or disconnected to 20 control the ionic current flow through them. Layers 3 and 4 add the ability to mechanically connect or disconnect the channels via the openings in Layer 2, forming the valves used to operate the device. The valves can take the form of mechanical valves, bridge rectifiers, or ionic diodes. Additionally, the mechanical valves can be actuated using Nitinol wire. In accordance with another aspect of the present invention, a method for delivering 25 direct current includes applying alternating current to electrodes immersed in an ionic 4 WO 2013/096574 PCT/US2012/070860 solution. The method also includes closing a first set of valves and switching a second set of valves in sequence and in phase with the alternating current. Additionally the method includes directing the direct current flow of ions into a target tissue. In accordance with yet another aspect of the present invention, the first set of valves 5 includes a first and second pair of valves and the second set of valves comprises a third and fourth pair of valves. The first and second set of valves are configured to be opened and closed and are further configured to switch in phase with alternating current applied to the electrodes. A conductor is used to direct the direct current flow of ions into the target tissue. The conductor includes a tube defining an elongate inner lumen, and the elongate inner 10 lumen of the tube is filled with a conductive material. The conductive material is an ionic solution or an ionic hydrogel. The method further includes closing the first set of valves when the third and fourth pair of valves are open, and closing the second set of valves when the first and second pairs of valves are open. 15 BRIEF DESCRIPTION OF THE DRAWINGS The accompanying drawings provide visual representations which will be used to more fully describe the representative embodiments disclosed herein and can be used by those skilled in the art to better understand them and their inherent advantages. In these drawings, like reference numerals identify corresponding elements and: 20 FIG. 1A illustrates a schematic diagram of the fundamental concept behind providing direct current stimulation to the tissue, while delivering alternating current to the metal electrodes within the device. Two states of the same system are shown. FIG. 1B demonstrates the periodic interruptions that occur at the system output from the prototype of the device described in Figure 1A. The interruptions occur at every phase 25 transition of the alternating current and valve states. 5 WO 2013/096574 PCT/US2012/070860 FIG. 2 illustrates a device for delivering direct current flow to target tissue and configured to eliminate current interruptions, according to an embodiment of the present invention. FIG. 3A illustrates the layer components for construction of the system described in 5 FIG. 2 according to an embodiment of the present invention. FIG. 3B illustrates the components of the system illustrated in FIG. 3A assembled into the finished device. FIG. 3C illustrates the location of the four metal electrodes relative to the other components of the device. 10 FIG. 4 illustrates a block diagram of electronics for the device, according to an embodiment of the present invention. FIG. 5 illustrates one of the two tube conductors (Tube electrode (TE)) used to deliver the ionic current from the device to the neural tissue, according to an embodiment of the present invention. 15 DETAILED DESCRIPTION The presently disclosed subject matter now will be described more fully hereinafter with reference to the accompanying Drawings, in which some, but not all embodiments of the inventions are shown. Like numbers refer to like elements throughout. The presently disclosed subject matter may be embodied in many different forms and should not be 20 construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will satisfy applicable legal requirements. Indeed, many modifications and other embodiments of the presently disclosed subject matter set forth herein will come to mind to one skilled in the art to which the presently disclosed subject matter pertains having the benefit of the teachings presented in the foregoing descriptions and 25 the associated Drawings. Therefore, it is to be understood that the presently disclosed subject 6 WO 2013/096574 PCT/US2012/070860 matter is not to be limited to the specific embodiments disclosed and that modifications and other embodiments are intended to be included within the scope of the appended claims. An embodiment in accordance with the present invention provides a device and method to deliver direct current to a target tissue, while also eliminating interruptions in 5 current flow. Two systems are used in tandem to deliver uninterrupted current to the neural tissue via two conductors. The two conductors (a.k.a. Tube electrode) are used to direct the flow of ionic current from the device into the target tissue. The first and second current producing systems are configured to be used together in order to eliminate the periodic interruptions in current flow. In use, one system drives current through the target tissue, while 10 the other system closes all of the valves first and then opens its valves in sequence. This intermediate step of closing all of the valves prevents unintended current shunts through either system. FIG. 2 illustrates a device for delivering direct current flow to target tissue and is configured to eliminate current interruptions, according to an embodiment of the present 15 invention. As illustrated in FIG. 2, the device 10 includes a left system 12 and a right system 14, both configured to deliver current to target tissue 16. The left system 12 includes a pair of electrodes 18, 20 and the right system 14 includes a pair of electrodes 22, 24. The electrodes 18, 20, and 22, 24 are configured to receive alternating current from current sources Il or 12 respectively. After the electrical current enters either the left system or the right system it 20 travels through a conductive material, such as saline, or any other suitable conductive material or solution known to one of skill in the art. The left system 12 includes valves Al, A2, B1, and B2, and the right system 14 includes valves C1, C2, D1, and D2. The valves can take the form of mechanical valves, other valve technology known to or conceivable by one of skill in the art. Additionally, the valves can be miniaturized using micro-electrical 25 mechanical miniaturization (MEMS) or other miniaturization technology. Valve Al is always 7 WO 2013/096574 PCT/US2012/070860 in the same state as valve A2, valve BI is always in the same state as valve B2 and so on. Additionally, FIG. 2 illustrates an example of flow of current 26 between electrodes 18 and 20 through the device 10 in order to deliver the current to the target tissue 16. In the example presented in FIG 2, the electric ionic current 26 flows easily through any open valve, 5 such as, for example in FIG. 2, valves B1, B2, D1, and D2 and not through the closed valves, such as indicated by valves Al, A2 and Cl and C2. As noted above, the device 10 uses a left system 12 and a right system 14. One system drives current through the tissue, while the other closes all valves first and then opens the next set of valves in sequence. Table 1, below, shows the states of the device 10 for different valve closures. The states are entered 10 sequentially and repeat after S12. The state of the device is indicated in the left column. The asterisks (*) indicate a switch in the current source that is controlling the flow through the tissue from the previous state. "0" indicates that the valve is closed. "1" indicates that the valve is open. Current sources Il, 12 can either control flow from upper electrode to the lower electrode in each of the two systems, indicated by "+"; lower to upper electrode indicated by 15 "-"; or be off, indicated by "0." It should also be noted that the direct current is delivered to the target tissue 16 from the top tube filled with conductive fluid to the bottom tube. 8 WO 2013/096574 PCT/US2012/070860 Table 1. *S2 0 0 0 1 1 0 0 1 1 + S3 0 0 0 0 0 0 0 1 1 + S4 0 1 1 0 0 0 0 1 1 + *S5 + 1 1 0 0 0 0 1 1 0 $6 + 1 1 0 0 0 0 0 0 57 + 1 1 0 0 10 O0 *S8 0 1 1 0 0 1 1 0 0 59 0 0 0 0 0 1 1 0 0 S10 0 0 0 1 1 1 1 0 0 *S1 - 0 0 1 1 1 1 0 0 0 $12 - 0 0 1 1 0 0 0 0 0 Although the device indicated by the FIG. 2 schematic can be built using different 5 methodologies, FIG. 3A illustrates one embodiment of the device and components for the construction of the present invention. FIG. 3B illustrates the components of the device illustrated in FIG. 3A assembled into the finished device, and FIG. 3C illustrates the location of the electrodes relative to the other components of the device. As illustrated in FIGS. 3A and 3C, layer 1, 28, includes electrodes 18, 20, 22, and 24, and channels through which the 10 current can flow through a saline solution. The channels correspond to those shown in FIG. 2. Layer 1 channels are filled with saline or an ionic hydrogel (such as based on Agar or gelatin) to conduct ionic current. Layer 2, 30, protects and covers layer 1, 28, and provides valve openings for the valves A1, A2, B1, B2, C1, C2, D1, and D2 to connect/disconnect the ionic current in the layer 1 channels. A thin layer of silicone, not shown, is used to cover 15 layer 2, 30, to insulate the saline/gel in the valves from valve plungers 32, disposed in layer 3, 34. Layer 3, 34, and layer 4, 36 include the valve plungers and Nitinol wires 38 used to 9 WO 2013/096574 PCT/US2012/070860 actuate the valves. Each of the Nitinol wires 38 actuates one pair of valves. All of the layers are formed from plastic or any other suitable material and glued together with water resistant glue, sealer, or other suitable adhesive. Further, as illustrated in FIG. 3B, the valves are driven by the Nitinol wires 38. When 5 electrically activated, using a microcontroller controlled electronic circuit, described further herein, the Nitinol wires decrease in length by 5%, allowing the intended valve to open. Each Nitinol wire 38 drives a pair of valve actuators, A, B, C, and D. The valve opens when the normally-closed actuator is deformed by tension applied to it through the 10Opm diameter Nitinol wire. The wire is shortened in length, when heated to 70-90' C by driving 180 mA 10 through the wire. The plunger 32 returns to its original position and lengthens the wire back to the original length when the current is off. The wire can undergo extraction-contraction cycles at up to 2 Hz. FIG. 4 illustrates a block diagram of electronics for the device, according to an embodiment of the present invention. A power block generates three power outputs. The first 15 power output is 60V, 2mA to drive the current sources Il and 12. The second is 3V, 30mA to support the electronics. The third is 1.5V, 800mA used to drive the Nitinol actuators. The valve drivers A, B, C, D maintain the current through the corresponding Nitinol actuators. 11/12 Current driver can direct current in either positive or negative direction through the corresponding pairs of electrodes. The differential amplifier detects the ion flow directed 20 through the tissue and sends the proportional voltage signal to the 11/12 current driver to control the output of the current source. The microcontroller (PC) controls the state machine of the device as indicated by Table 1. Two tube electrodes (conductors) are used, as illustrated in FIG. 5 to carry the direct ionic current from the device to the stimulated tissue. This figure shows the one such 25 embodiment of the tube electrodes compared to a typical PtIr wire electrode used in neural 10 WO 2013/096574 PCT/US2012/070860 stimulation. These tube conductors can be prepared by filling (TE) Eppendorf 20pL capillary tubes (0.25mm OD, 0.2mm ID) with a sterile mixture of agar and ionic solution. While the gel freely conducts the ionic current, it resists fluid motion in and out of the tube and it offers a physical barrier to biological contamination of the implanted tissue. 5 Far reaching plans to advance safe DC stimulation include use of ionic diodes or ionic transistors that could modulate ionic conductance to control ionic current flow instead of mechanical valves. The ionic diode technology is quickly evolving to create semi-permeable membranes that are constructed to allow flow of ions in one direction but block the flow in the opposite direction. Because mechanical valves are the highest power consuming elements 10 in the SDCS, using ionic diodes that consume no power at all will significantly reduce power of the overall safe DC system. Ionic diodes can be used instead of the valves in the safe DC system construction in a way that is analogous to the use of diodes in a bridge rectifier configuration. A bridge rectifier is a 4-diode electronic component commonly used in power supplies to switch AC to DC power. The ionic diodes will control ion flow instead of electron 15 current flow controlled by conventional diodes. Assuming the ionic diodes can be reduced in size, more extreme miniaturization of the described technology will also enable multiple stimulation channels to be delivered simultaneously to different stimulation targets because several separate safe DC stimulators could be assembled on one device. 20 The many features and advantages of the invention are apparent from the detailed specification, and thus, it is intended by the appended claims to cover all such features and advantages of the invention which fall within the true spirit and scope of the invention. Further, since numerous modifications and variations will readily occur to those skilled in the art, it is not desired to limit the invention to the exact construction and operation illustrated 25 and described, and accordingly, all suitable modifications and equivalents may be resorted to, 11 WO 2013/096574 PCT/US2012/070860 falling within the scope of the invention. Although the present invention has been described in connection with preferred embodiments thereof, it will be appreciated by those skilled in the art that additions, deletions, modifications, and substitutions not specifically described may be made without 5 departing from the spirit and scope of the invention as defined in the appended claims. 12
权利要求:
Claims (20)
[1] 1. A device for delivering direct current, comprising: a first set of two electrodes and a second set of two electrodes configured to receive alternating current; 5 a first set of valves, wherein the first set of valves comprises a first and second pair of valves, and a second set of valves, wherein the second set of valves comprises a third and fourth pair of valves, where the first and second sets of valves are configured to be opened and closed and are further configured to switch in phase with the alternating current applied to the first electrode and the second electrode; 10 a tube filled with conductive material and configured to direct the direct current flow of ions into target tissue; and wherein the device is configured such that the first set of valves is closed when the third and fourth pairs of valves are being opened and the second set of valves is closed when the first and second pairs of valves are being opened. 15
[2] 2. The device of claim 1 wherein the conductor comprises a tube defining a hollow lumen extending therethrough.
[3] 3. The device of claim 2 wherein the hollow lumen of the tube is filled with a 20 conductive material.
[4] 4. The device of claim 3 wherein the conductive material is an ionic solution or an ionic hydrogel. 25
[5] 5. The device of claim 1 further comprising a housing. 13 WO 2013/096574 PCT/US2012/070860
[6] 6. The device of claim 5 wherein the housing comprises layers.
[7] 7. The device of claim 6 wherein each one of the layers of the housing contains one of 5 the electrodes and the first set of valves and the second set of valves.
[8] 8. The device of claim 1 wherein the valves comprise mechanical valves.
[9] 9. The device of claim 8 wherein the mechanical valves comprise Nitinol wire. 10
[10] 10. The device of claim 1 wherein the valves comprise a bridge rectifier.
[11] 11. The device of claim 1 wherein the valves comprise an ionic diode. 15
[12] 12. A method for delivering direct current comprising: applying alternating current to electrodes immersed in an ionic solution; closing a first set of valves; switching a second set of valves in sequence and in phase with the alternating current; and 20 directing the direct current flow of ions into a target tissue.
[13] 13. The method of claim 12 wherein the first set of valves comprises a first and second pair of valves and the second set of valves comprises a third and fourth pair of valves. 25
[14] 14. The method of claim 12 wherein the first and second set of valves are configured to 14 WO 2013/096574 PCT/US2012/070860 be opened and closed and are further configured to switch in phase with alternating current applied to the electrodes.
[15] 15. The method of claim 12 further comprising using a conductor to direct the direct 5 current flow of ions into the target tissue.
[16] 16. The method of claim 12 wherein the conductor comprises a tube defining an elongate inner lumen. 10
[17] 17. The method of claim 16 wherein the elongate inner lumen of the tube is filled with a conductive material.
[18] 18. The method of claim 17 wherein the conductive material is an ionic solution or an ionic hydrogel. 15
[19] 19. The method of claim 13 further comprising closing the first set of valves when the third and fourth pair of valves are open.
[20] 20. The method of claim 13 further comprising closing the second set of valves when the 20 first and second pairs of valves are open. 15
类似技术:
公开号 | 公开日 | 专利标题
US10258793B2|2019-04-16|Artifact control and miniaturization of the safe direct current stimulator for neural prostheses
US9375575B2|2016-06-28|Short duration pre-pulsing to reduce stimulation-evoked side-effetcs
US8639351B2|2014-01-28|Systems and methods for adjusting electrical therapy based on impedance changes
Fridman et al.2013|Safe direct current stimulation to expand capabilities of neural prostheses
JP5802218B2|2015-10-28|System and method for independently operating multiple neural stimulation channels
US9737703B2|2017-08-22|Method to enhance afferent and efferent transmission using noise resonance
AU2018249498A1|2019-10-24|Systems and methods for direct current nerve conduction block
CA3091769A1|2019-08-29|Methods and systems for nerve conduction block
AU2019299334A1|2021-01-21|Systems and methods for nerve conduction block
Van Dongen et al.2016|Design of Efficient and Safe Neural Stimulators
US8843208B2|2014-09-23|Variable impedance shunt for a tissue stimulating prosthesis
US20210370071A1|2021-12-02|Safe direct current stimulator design for reduced power and increased reliability
Dongen et al.2016|System Design of Neural Stimulators
CN108028996B|2021-01-12|Method and system for micro-charge stimulation
Noorsal et al.2015|Multichannel microstimulating SoC
Banerjee et al.2020|Energy-Efficient Electrical Stimulation Systems
Liu et al.2011|Neural interfaces for implanted stimulators
同族专利:
公开号 | 公开日
US9572979B2|2017-02-21|
US20170203099A1|2017-07-20|
EP2793998A1|2014-10-29|
AU2012358886B2|2017-10-19|
WO2013096574A1|2013-06-27|
US10258793B2|2019-04-16|
US20140364796A1|2014-12-11|
EP2793998A4|2015-06-03|
CN104168950A|2014-11-26|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题
WO1993009843A1|1991-11-15|1993-05-27|Schoendorf Erhard|Electrotherapy apparatus|
WO2001058393A1|2000-02-11|2001-08-16|Potencia Medical Ag|Impotence treatment apparatus with energy transforming means|
US20060025757A1|2004-07-20|2006-02-02|Heim Warren P|Multielectrode electrosurgical instrument|
US7896875B2|2004-07-20|2011-03-01|Microline Surgical, Inc.|Battery powered electrosurgical system|
US20060136007A1|2004-12-21|2006-06-22|Mickle Marlin H|Deep brain stimulation apparatus, and associated methods|
US7896874B2|2005-12-29|2011-03-01|Boston Scientific Scimed, Inc.|RF ablation probes with tine valves|
US8311640B2|2008-09-04|2012-11-13|Cochlear Limited|Variable impedance bypass pathway for a tissue stimulating prosthesis|
US9008800B2|2009-11-23|2015-04-14|Case Western Reserve University|Separated-interface nerve electrode|
KR20120125568A|2010-01-12|2012-11-15|더 존스 홉킨스 유니버시티|Implantable vestibular prosthesis|
CN101953647B|2010-07-28|2013-05-01|广东新宝电器股份有限公司|Soymilk grinder/ juicer with milling function|EP3669933A1|2010-02-26|2020-06-24|Cornell University|Retina prosthesis|
US9302103B1|2010-09-10|2016-04-05|Cornell University|Neurological prosthesis|
CN103890781B|2011-08-25|2017-11-21|康奈尔大学|Retina encoder for machine vision|
US10864373B2|2015-12-15|2020-12-15|Case Western Reserve University|Systems for treatment of a neurological disorder using electrical nerve conduction block|
US10195434B2|2012-06-15|2019-02-05|Case Western Reserve University|Treatment of pain using electrical nerve conduction block|
EP3283163B1|2015-04-15|2019-10-02|Pixium Vision|Pixel cell circuit and implant|
EP3291780A4|2015-04-20|2019-01-23|Cornell University|Machine vision with dimensional data reduction|
AU2018249498A1|2017-04-03|2019-10-24|Presidio Medical, Inc.|Systems and methods for direct current nerve conduction block|
法律状态:
2018-02-15| FGA| Letters patent sealed or granted (standard patent)|
优先权:
申请号 | 申请日 | 专利标题
US201161577821P| true| 2011-12-20|2011-12-20||
US61/577,821||2011-12-20||
PCT/US2012/070860|WO2013096574A1|2011-12-20|2012-12-20|Artifact control and miniaturization of the safe direct current stimulator for neural prostheses|
[返回顶部]