CN113180885A - Optic nerve interface and its preparing method - Google Patents
Optic nerve interface and its preparing method Download PDFInfo
- Publication number
- CN113180885A CN113180885A CN202110356350.1A CN202110356350A CN113180885A CN 113180885 A CN113180885 A CN 113180885A CN 202110356350 A CN202110356350 A CN 202110356350A CN 113180885 A CN113180885 A CN 113180885A
- Authority
- CN
- China
- Prior art keywords
- optic nerve
- monofilaments
- interface
- conduit
- nerve
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 210000001328 optic nerve Anatomy 0.000 title claims abstract description 46
- 238000000034 method Methods 0.000 title claims description 7
- 210000005036 nerve Anatomy 0.000 claims abstract description 18
- 238000001727 in vivo Methods 0.000 claims abstract description 5
- 239000007769 metal material Substances 0.000 claims abstract description 5
- 230000001537 neural effect Effects 0.000 claims description 11
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 8
- 229910052737 gold Inorganic materials 0.000 claims description 8
- 239000010931 gold Substances 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 7
- 229920000620 organic polymer Polymers 0.000 claims description 6
- 238000009941 weaving Methods 0.000 claims description 5
- 230000000694 effects Effects 0.000 claims description 3
- 108010022355 Fibroins Proteins 0.000 claims description 2
- 239000000835 fiber Substances 0.000 abstract description 19
- 238000002360 preparation method Methods 0.000 abstract description 8
- 208000017442 Retinal disease Diseases 0.000 abstract description 6
- 206010038923 Retinopathy Diseases 0.000 abstract description 6
- 208000029257 vision disease Diseases 0.000 abstract description 5
- 210000003050 axon Anatomy 0.000 abstract description 3
- 239000002657 fibrous material Substances 0.000 abstract 1
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 abstract 1
- 210000004126 nerve fiber Anatomy 0.000 description 5
- 206010047571 Visual impairment Diseases 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 210000001525 retina Anatomy 0.000 description 2
- 210000003497 sciatic nerve Anatomy 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 108010013296 Sericins Proteins 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 210000005252 bulbus oculi Anatomy 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 210000000349 chromosome Anatomy 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010166 immunofluorescence Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 231100000915 pathological change Toxicity 0.000 description 1
- 230000036285 pathological change Effects 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000002207 retinal effect Effects 0.000 description 1
- 238000011222 transcriptome analysis Methods 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/02—Inorganic materials
- A61L27/04—Metals or alloys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/02—Inorganic materials
- A61L27/04—Metals or alloys
- A61L27/047—Other specific metals or alloys not covered by A61L27/042 - A61L27/045 or A61L27/06
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/22—Polypeptides or derivatives thereof, e.g. degradation products
- A61L27/227—Other specific proteins or polypeptides not covered by A61L27/222, A61L27/225 or A61L27/24
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2240/00—Manufacturing or designing of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2240/001—Designing or manufacturing processes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2430/00—Materials or treatment for tissue regeneration
- A61L2430/32—Materials or treatment for tissue regeneration for nerve reconstruction
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Medicinal Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Ophthalmology & Optometry (AREA)
- Cardiology (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Materials For Medical Uses (AREA)
- Prostheses (AREA)
Abstract
The invention relates to the field of biological nerves, in particular to an optic nerve interface and a preparation method thereof. The invention adopts silk fiber and metal material to make a nerve interface which can be connected with optic nerve, the optic nerve axon grows along the gap and can be connected with a lead wire made of metal material through the interface, thereby the optic nerve and the implanted type instrument are connected into reality, and the vision of the patient with visual disorder caused by retinopathy can be recovered. The implanted optic nerve interface researched by the invention has good biocompatibility, is not degraded in vivo for a long time, establishes a one-to-one corresponding relation between the conducting wire and each optic nerve fiber, acquires more direct and accurate signals, and can recover vision of a patient with visual disorder caused by retinopathy.
Description
Technical Field
The invention relates to the field of biological nerves, in particular to an optic nerve interface and a preparation method thereof.
Background
The optical system, retina, optic nerve and visual center of vision are formed, and the lesion of any link can cause visual disturbance. There are many clinical treatments for the pathological changes of the optical system. Visual disturbances caused by retinopathy, optic nerve and central vision disorders are troublesome, with those caused by retinopathy being the most common.
There are many approaches to dealing with the visual disturbance caused by retinopathy. These concepts mainly include two broad categories, one of which is to facilitate retinal repair from a purely medical perspective, and the other of which is to assist the patient in forming vision from the perspective of medical instruments. There are two main strategies in the study of assisting patients with medical devices to establish vision, namely implantable and non-implantable devices. The implanted instrument has good effect but higher difficulty; non-implantable devices circumvent some medical difficulties, but the effect is less than ideal.
The difficulty of implantable devices is that the retina and the visual center are composed of hundreds of millions of cells, and the structures are very complex and basically difficult to reach by manpower. The structure of the optic nerve consists of approximately 5000 nerve fibers, and it is relatively easy to restore the vision of a visually impaired patient starting from the optic nerve. Therefore, it is very important to explore a superior material capable of replacing nerves and a corresponding connection mode, and how to connect the nerves with an implanted instrument becomes a problem to be solved urgently.
Disclosure of Invention
The invention provides an optic nerve interface and a preparation method thereof for solving the problems, and the optic nerve interface is developed by using the good biocompatibility of silk fiber.
One of the objectives of the present invention is to provide an optic nerve interface, which has the following specific technical scheme:
an optic nerve interface, which comprises a conduit, monofilaments and a lead, wherein the conduit is in a tubular shape formed by weaving the monofilaments, the monofilaments piled up in a bundle shape are contained in the conduit, and the lead is positioned in a gap formed between the monofilaments; the nerve end connected with the catheter is provided with a cavity, and the guide wire is made of metal materials.
Preferably, the monofilament is a monofilament in natural cocoon silk fiber, and is made of raw silk through degumming treatment, and the diameter of the monofilament is 15-28 μm.
Preferably, the monofilament diameter is 18 μm.
Preferably, the inner diameter of the catheter is the same as the outer diameter of the optic nerve.
Preferably, the number of filaments and the number of slits contained in the catheter are equal to n, which is the total number of nerve fibers in the optic nerve ± 500.
Preferably, the wire is made of metal with good ductility and excellent conductivity, such as gold, platinum or silver, by step-by-step stretching, and the diameter of the wire is 5-10 μm.
Preferably, the wire is made of gold material and has a diameter of 8 μm.
Preferably, the length of the cavity is 2-20 mm.
Preferably, the cavity has a length of 20 mm.
Preferably, the outer surface of the lead is wrapped by an organic polymer, and the organic polymer has the performance of electric insulation, difficult degradation in vivo and good biocompatibility.
The second purpose of the present invention is to provide a method for preparing the neural interface, which comprises the following specific technical scheme:
a method for preparing an optic nerve interface, comprising the following steps:
(1) weaving the monofilaments to obtain the catheter;
(2) stacking monofilaments within the conduit;
(3) adding metal wires into the piled monofilament gaps;
(4) the nerve end connected with the catheter is provided with a cavity.
Furthermore, the number of monofilaments and the number of slits contained in the catheter are the same, and are both n, which is the total number of nerve fibers in the optic nerve +/-500.
Preferably, 5000 monofilaments are contained in the catheter, the number of the gaps is 5000, and the number of the wires is 5000.
Further, the monofilament is made of raw silk by degumming and has a diameter of 15-28 μm.
The metal wire with the diameter of about 5-10 mu m is preset in the optic nerve interface, so that the information communication between the nerve fiber message and external equipment can be ensured.
The invention has the advantages that: the implanted optic nerve interface researched by the invention adopts the silk fiber which has good biocompatibility and is not degraded in vivo for a long time to develop the nerve interface, and the acquired signals are more direct, accurate and complete. Compared with the neural interface for recovering the visual disorder, the implanted type optic nerve interface researched by the invention establishes a one-to-one corresponding relation with each optic nerve fiber, so that the vision of the patient with the visual disorder caused by retinopathy can be recovered.
Drawings
FIG. 1 is a flow chart of the preparation of the neural interface of the present invention
FIG. 2 is a diagram of an application scenario of the neural interface of the present invention
FIG. 3 is the NF200 immunofluorescence chromosome observation chart of rat optic nerve cross section
FIG. 4 is a transmission electron microscope photograph of the cross section of the mouse optic nerve in the example
FIG. 5 is a graph showing the growth of rat sciatic nerve fibers in the gap formed by silk fibers in the example
In the figure, 1-lead, 2-monofilament, 3-conduit, 4-nerve fiber, 5-optic nerve, 6-signal conversion device, 7-wireless signal transmitter, 8-brain-machine interface and wireless signal receiver, 9-microchannel.
Detailed Description
The present invention will be described in further detail with reference to the following examples and drawings, it being understood that the present invention is not limited to the particular examples described herein, but is capable of modification in various forms and details, and can be modified within the spirit and scope of the invention.
Fig. 2 is a research object of the present invention, even if the vision-impaired patient restores vision by implanting a brain-machine interface, which is a technical problem that the brain-machine interface needs to overcome, in cooperation with an external device, the present invention adopts silk fibers with good biocompatibility and no degradation in vivo for a long time to develop a nerve interface, and uses metals to make conducting wires, such as yellow, silver, copper and other conducting metals.
DETAILED DESCRIPTION OF EMBODIMENT (S) OF INVENTION
(1) Study of rat optic nerve Structure
Rat optic nerves were taken, transected, and observed with a transmission electron microscope. The nerve fibers were counted and analyzed for shape, diameter and arrangement.
(2) Preparation of silk monofilament fiber
Boiling the cooked silk with dilute alkali, and removing sericin to obtain monofilament fiber for later use.
(3) Preparation of metal wire from gold
A series of pores with gradient diameters are preset on a metal plate, the minimum pore diameter is 8 mu m, gold wires are gradually stretched and extruded in the pores, and the metal wires with the diameter of 8 mu m are finally prepared by utilizing the excellent ductility of the gold. The wires are treated with an organic polymer and coated with a layer of insulating material on the outer surface for use.
(4) Preparation of optic nerve interface
Weaving a conduit with the inner diameter of 700 mu m by using monofilament fibers; placing about 5000 monofilaments in the catheter, wherein the monofilament fibers are piled up into a bundle, about 5000 gaps are formed among the monofilaments, and each gap can just accommodate 1 optic nerve fiber to grow in the gap; one side (2 mm from the end) of each slit is preset with 1 wire (total of about 5000 wires, diameter about 8 μm) to prepare the optic nerve interface, as shown in fig. 1, wherein the 2mm space reserved in each slit is for optic nerve fiber ingrowth until the wire is connected. After the optic nerve is transected, the section is inserted into a cavity reserved in the catheter, and the axons of the optic nerve grow along the gaps until the axons are connected with the guide wire, so that the aim that each optic nerve fiber is connected with one guide wire is fulfilled.
The prepared neural interface is shown in figure 1 and comprises a tubular catheter woven by monofilaments, the monofilaments and a lead, wherein the monofilaments which are piled up into bundles are contained in the catheter, and the lead is positioned in a gap formed between the monofilaments and is made of a metal material; the nerve end connected with the catheter is provided with a cavity. The monofilament is made of silk fibroin and has a diameter of 18 μm; the inner diameter of the conduit is 700 mu m; the catheter contains 5000 monofilaments, the number of the gaps is 5000, and the number of the wires is 5000. The wire is made of gold material and has a diameter of 8 μm. The length of the cavity is 2 mm. The outer surface of the lead is wrapped with organic polymer to play a role of insulation.
(5) Biocompatible detection of optic nerve interface
The optic nerve of the rat is cut off, and the optic nerve interfaces are respectively implanted at the broken ends of the optic nerve facing to the eyeball side and the brain side. And (3) obtaining materials at a series of time points, performing morphological observation, transcriptome analysis and bioelectricity detection, taking the materials as a basis for judging the biocompatibility of the optic nerve interface, and adjusting the preparation scheme of the optic nerve interface on the basis of the basis.
It can be seen from fig. 3-5 that rat sciatic nerve fibers grow well in the gap formed by the silk fibers, thereby verifying the feasibility of the invention for preparing the nerve interface by using the silk fibers, and explaining that the diameters of specific guide lines and guide pipes, the size of the reserved gap and the like are the prerequisite guarantees, after all, the optic nerve is simpler than other nerves, and if the nerve interface is applied to other nerves, specific parameters of the guide pipes, the guide lines, the monofilament gaps and the cavities (reserved growth spaces) need to be further explored.
The above description is only for the purpose of illustrating the preferred embodiments of the present invention and is not to be construed as limiting the invention, and any modifications, equivalents, improvements and the like that fall within the spirit and principle of the present invention are intended to be included therein.
Claims (10)
1. An optic nerve interface, characterized in that, the nerve interface comprises a conduit, monofilaments and a lead, the conduit is in a tubular shape formed by weaving the monofilaments, the monofilaments piled up in a bundle shape are contained in the conduit, and the lead is positioned in a gap formed between the monofilaments; the nerve end connected with the catheter is provided with a cavity, and the guide wire is made of metal materials.
2. The neural interface of claim 1, wherein the monofilaments are monofilaments of natural silk fibres having a diameter of 15-28 μm.
3. The neural interface of claim 1, wherein the inner diameter of the conduit is the same as the outer diameter of the optic nerve.
4. The neural interface of claim 1, wherein the number of monofilaments and the number of slits contained within the conduit are the same.
5. The neural interface of claim 1, wherein the leads are made of gold material and have a diameter of 5-10 μm.
6. The neural interface of claim 1, wherein the cavity is 2-20mm in length.
7. The neural interface as claimed in claim 1, wherein the outer surface of the lead is coated with an organic polymer, and the organic polymer has an electrical insulating effect, is difficult to degrade in vivo, and has good biocompatibility.
8. A method for preparing an optic nerve interface, comprising the following steps:
(1) weaving the monofilaments to obtain the catheter;
(2) stacking monofilaments within the conduit;
(3) adding metal wires into the piled monofilament gaps;
(4) the nerve end connected with the catheter is provided with a cavity.
9. The method of claim 8, wherein the number of filaments and the number of slits contained in the conduit are the same.
10. The method of claim 8, wherein the monofilaments are made of silk fibroin and have a diameter of 18 μm; the lead is made of gold material and has a diameter of 5-10 μm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110356350.1A CN113180885A (en) | 2021-04-01 | 2021-04-01 | Optic nerve interface and its preparing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110356350.1A CN113180885A (en) | 2021-04-01 | 2021-04-01 | Optic nerve interface and its preparing method |
Publications (1)
Publication Number | Publication Date |
---|---|
CN113180885A true CN113180885A (en) | 2021-07-30 |
Family
ID=76974472
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202110356350.1A Pending CN113180885A (en) | 2021-04-01 | 2021-04-01 | Optic nerve interface and its preparing method |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN113180885A (en) |
Citations (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1340363A (en) * | 2000-09-01 | 2002-03-20 | 肖志成 | Bioabsorbable lead and catheter facilitating regeneration of ruptured nerve |
CN1911470A (en) * | 2006-07-28 | 2007-02-14 | 中国科学院上海微系统与信息技术研究所 | Implantation micro-electrode having integrated medicinal agent releasing function, its manufacturing method and application |
CN1961850A (en) * | 2006-12-07 | 2007-05-16 | 上海交通大学 | Implantable vision prosthesis |
CN101006953A (en) * | 2007-01-18 | 2007-08-01 | 上海交通大学 | Artificial retina neural flexible microelectrode array chips and processing method thereof |
CN101396583A (en) * | 2008-10-30 | 2009-04-01 | 上海交通大学 | Vision prosthesis device based on optical-disc micro-electrode array |
CN101579246A (en) * | 2009-05-31 | 2009-11-18 | 苏州大学 | Artificial silk fibroin nano-fiber nerve repair conduit and preparation method thereof |
CN102638013A (en) * | 2012-04-25 | 2012-08-15 | 成都森源开关有限公司 | Target image identification transmission line state monitoring system based on visual attention mechanism |
CN102793592A (en) * | 2012-08-09 | 2012-11-28 | 上海交通大学 | Optic nerve implantable neural interface device with fan-shaped attaching function |
CN103877623A (en) * | 2014-02-19 | 2014-06-25 | 西南大学 | Tissue engineered artificial nerve and preparation method thereof |
CN104548345A (en) * | 2015-01-16 | 2015-04-29 | 上海交通大学 | Elastic self-curling coating nerve-implantable connector device and manufacturing method thereof |
CN105496643A (en) * | 2016-01-18 | 2016-04-20 | 戴国群 | Intelligent wearing device for vision recovery of patient with posteriority blindness and making method thereof |
CN105833340A (en) * | 2016-05-31 | 2016-08-10 | 河北医科大学第三医院 | Nerve conduit with function of nerve regeneration promotion |
CN106794281A (en) * | 2014-09-10 | 2017-05-31 | 卢森堡科学技术研究院 | Implantable electrode |
CN107835655A (en) * | 2015-07-24 | 2018-03-23 | 韩国科学技术研究院 | Minimize the high-performance nerve probe structure of neurotrosis |
CN107961437A (en) * | 2018-01-09 | 2018-04-27 | 西安交通大学 | A kind of implantating biological type brain electrode multistage propulsion system and its operating method |
CN108136174A (en) * | 2015-04-17 | 2018-06-08 | 穆贾拉医疗私人有限公司 | implantable nerve stimulation device |
CN108904972A (en) * | 2017-04-14 | 2018-11-30 | 上海交通大学 | A kind of embedded nerve electrode based on carbon nano tube line |
CN109395167A (en) * | 2018-12-10 | 2019-03-01 | 重庆市畜牧科学院 | Degradable silk artificial neuron |
CN209519145U (en) * | 2018-12-24 | 2019-10-22 | 巴斯特医药科技(常州)有限公司 | Needle holder being applied to surgery Minimally nerve trachea |
CN110841186A (en) * | 2019-11-19 | 2020-02-28 | 华中科技大学 | Implanted peripheral nerve electrode |
CN111132726A (en) * | 2017-04-18 | 2020-05-08 | 墨尔本大学 | Intravascular device for sensing and/or stimulating tissue |
CN111297513A (en) * | 2020-03-19 | 2020-06-19 | 中国海洋大学 | Artificial nerve conduit loaded with trophic factors and preparation method and application thereof |
CN111671979A (en) * | 2020-08-12 | 2020-09-18 | 上海白衣缘生物工程有限公司 | Nerve repair material |
CN111904493A (en) * | 2020-08-14 | 2020-11-10 | 广东省人民医院 | Nerve retractor device |
CN112263714A (en) * | 2020-10-15 | 2021-01-26 | 苏州大学 | Silk protein nerve conduit and preparation method thereof |
CN112402689A (en) * | 2020-11-17 | 2021-02-26 | 武汉理工大学 | Conductive nerve repair system filled with double-drug-loading nanofiber and preparation method thereof |
-
2021
- 2021-04-01 CN CN202110356350.1A patent/CN113180885A/en active Pending
Patent Citations (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1340363A (en) * | 2000-09-01 | 2002-03-20 | 肖志成 | Bioabsorbable lead and catheter facilitating regeneration of ruptured nerve |
CN1911470A (en) * | 2006-07-28 | 2007-02-14 | 中国科学院上海微系统与信息技术研究所 | Implantation micro-electrode having integrated medicinal agent releasing function, its manufacturing method and application |
CN1961850A (en) * | 2006-12-07 | 2007-05-16 | 上海交通大学 | Implantable vision prosthesis |
CN101006953A (en) * | 2007-01-18 | 2007-08-01 | 上海交通大学 | Artificial retina neural flexible microelectrode array chips and processing method thereof |
CN101396583A (en) * | 2008-10-30 | 2009-04-01 | 上海交通大学 | Vision prosthesis device based on optical-disc micro-electrode array |
CN101579246A (en) * | 2009-05-31 | 2009-11-18 | 苏州大学 | Artificial silk fibroin nano-fiber nerve repair conduit and preparation method thereof |
CN102638013A (en) * | 2012-04-25 | 2012-08-15 | 成都森源开关有限公司 | Target image identification transmission line state monitoring system based on visual attention mechanism |
CN102793592A (en) * | 2012-08-09 | 2012-11-28 | 上海交通大学 | Optic nerve implantable neural interface device with fan-shaped attaching function |
CN103877623A (en) * | 2014-02-19 | 2014-06-25 | 西南大学 | Tissue engineered artificial nerve and preparation method thereof |
CN106794281A (en) * | 2014-09-10 | 2017-05-31 | 卢森堡科学技术研究院 | Implantable electrode |
CN104548345A (en) * | 2015-01-16 | 2015-04-29 | 上海交通大学 | Elastic self-curling coating nerve-implantable connector device and manufacturing method thereof |
CN108136174A (en) * | 2015-04-17 | 2018-06-08 | 穆贾拉医疗私人有限公司 | implantable nerve stimulation device |
CN107835655A (en) * | 2015-07-24 | 2018-03-23 | 韩国科学技术研究院 | Minimize the high-performance nerve probe structure of neurotrosis |
CN105496643A (en) * | 2016-01-18 | 2016-04-20 | 戴国群 | Intelligent wearing device for vision recovery of patient with posteriority blindness and making method thereof |
CN105833340A (en) * | 2016-05-31 | 2016-08-10 | 河北医科大学第三医院 | Nerve conduit with function of nerve regeneration promotion |
CN108904972A (en) * | 2017-04-14 | 2018-11-30 | 上海交通大学 | A kind of embedded nerve electrode based on carbon nano tube line |
CN111132726A (en) * | 2017-04-18 | 2020-05-08 | 墨尔本大学 | Intravascular device for sensing and/or stimulating tissue |
CN107961437A (en) * | 2018-01-09 | 2018-04-27 | 西安交通大学 | A kind of implantating biological type brain electrode multistage propulsion system and its operating method |
CN109395167A (en) * | 2018-12-10 | 2019-03-01 | 重庆市畜牧科学院 | Degradable silk artificial neuron |
CN209519145U (en) * | 2018-12-24 | 2019-10-22 | 巴斯特医药科技(常州)有限公司 | Needle holder being applied to surgery Minimally nerve trachea |
CN110841186A (en) * | 2019-11-19 | 2020-02-28 | 华中科技大学 | Implanted peripheral nerve electrode |
CN111297513A (en) * | 2020-03-19 | 2020-06-19 | 中国海洋大学 | Artificial nerve conduit loaded with trophic factors and preparation method and application thereof |
CN111671979A (en) * | 2020-08-12 | 2020-09-18 | 上海白衣缘生物工程有限公司 | Nerve repair material |
CN111904493A (en) * | 2020-08-14 | 2020-11-10 | 广东省人民医院 | Nerve retractor device |
CN112263714A (en) * | 2020-10-15 | 2021-01-26 | 苏州大学 | Silk protein nerve conduit and preparation method thereof |
CN112402689A (en) * | 2020-11-17 | 2021-02-26 | 武汉理工大学 | Conductive nerve repair system filled with double-drug-loading nanofiber and preparation method thereof |
Non-Patent Citations (9)
Title |
---|
DAVIAUD, NICOLAS;CHEN, KAREN;HUANG, YONG: "Impaired cortical neurogenesis in plexin-B1 and-B2 double deletion mutant", vol. 76, no. 8, pages 882 - 899, XP072441002, DOI: 10.1002/dneu.22364 * |
LIU, BIN;SONG, YU-WEI;JIN, LI: "Silk structure and degradation", vol. 131, pages 122 - 128, XP029179068, DOI: 10.1016/j.colsurfb.2015.04.040 * |
ZHOU, CHAN;LIU, BIN;HUANG, YONG: "The effect of four types of artificial nerve graft structures on the repair of 10-mm rat sciatic nerve gap", vol. 105, no. 11, pages 3077 - 3085 * |
周婵,刘彬,王介平,吕金凤,王海燕,曾秀.: "家蚕丝素蛋白在组织工程中的应用研究进展", vol. 49, no. 23, pages 91 - 94 * |
康晓洋: "面向瘫痪康复的氧化铱柔性可植入MEMS神经接口器件研究" * |
李晋,曾秀,吕金凤: "蚕丝的结构、性质和应用", pages 153 - 153 * |
王乐军,黄勇,龚铭新: "小波包分析与人工神经网络相结合探索运动性肌肉疲劳过程中sEMG变化特征", vol. 29, no. 12, pages 51 - 55 * |
王孜,许俊敏,王介平: "非动脉炎性前部缺血性视神经病变视盘形态学定量研究", vol. 28, no. 7, pages 735 - 737 * |
王晶晶,黄勇,陈宝欣,赵运勇.: "基于独立循环神经网络的跌倒检测方法", vol. 39, no. 07, pages 20 - 23 * |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FitzGerald et al. | A regenerative microchannel neural interface for recording from and stimulating peripheral axons in vivo | |
CN101396583B (en) | Vision prosthesis device based on optical-disc micro-electrode array | |
Lacour et al. | Long micro-channel electrode arrays: a novel type of regenerative peripheral nerve interface | |
US7818065B2 (en) | Conducting polymer nanowire brain-machine interface systems and methods | |
US9283386B2 (en) | Neural element comprising nanowires and support layer | |
CN100558426C (en) | Implantable sheet type optic nerve micro stimulating electrode | |
CN101888873A (en) | Medical electrode, electrode bundle and electrode bundle array | |
WO2008048237A2 (en) | Braided electrodes | |
CN107961437A (en) | A kind of implantating biological type brain electrode multistage propulsion system and its operating method | |
US8639311B2 (en) | Sensing probe comprising multiple, spatially separate, sensing sites | |
CN106963358A (en) | A kind of embedded nerve electrode based on carbon nano tube line | |
Lewitus et al. | Designing tyrosine-derived polycarbonate polymers for biodegradable regenerative type neural interface capable of neural recording | |
KR102163164B1 (en) | Nanofiber mesh bioelectrode, and method for producing the same | |
Kim et al. | Braided multi-electrode probes: mechanical compliance characteristics and recordings from spinal cords | |
CN102793592B (en) | Optic nerve implantable neural interface device with fan-shaped attaching function | |
CN1973918B (en) | Cluster stimulating micro electrode array capable of being implanted into nerve system of human body | |
CN109124807A (en) | A kind of rat spinal motor reconstruction method based on time coherence stimulation | |
CN111787973A (en) | Nerve monitoring and/or stimulation electrode assembly | |
US11992319B2 (en) | Method of making a neural interface system | |
US20120259388A1 (en) | Annular electrode array | |
Hu et al. | Bioactive polymer-enabled conformal neural interface and its application strategies | |
CN113180885A (en) | Optic nerve interface and its preparing method | |
Kotamraju et al. | Selective chronic recording in small nerve fascicles of sciatic nerve with carbon nanotube yarns in rats | |
US11406816B2 (en) | System and methods for percutaneous mechanical and/or neural interface | |
WO2021118457A1 (en) | Implantable guide element and methods of fabrication and use thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination |