CN106237382A - Promote CO2 laser weld pipe and preparation method thereof - Google Patents

Promote CO2 laser weld pipe and preparation method thereof Download PDF

Info

Publication number
CN106237382A
CN106237382A CN201610729307.4A CN201610729307A CN106237382A CN 106237382 A CN106237382 A CN 106237382A CN 201610729307 A CN201610729307 A CN 201610729307A CN 106237382 A CN106237382 A CN 106237382A
Authority
CN
China
Prior art keywords
laser weld
weld pipe
rush
pipe
gelatin
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
Application number
CN201610729307.4A
Other languages
Chinese (zh)
Inventor
苟马玲
魏于全
胡喻
苟智元
陶杰
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sichuan University
Original Assignee
Sichuan University
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sichuan University filed Critical Sichuan University
Priority to CN201610729307.4A priority Critical patent/CN106237382A/en
Publication of CN106237382A publication Critical patent/CN106237382A/en
Pending legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/14Macromolecular materials
    • A61L27/22Polypeptides or derivatives thereof, e.g. degradation products
    • A61L27/222Gelatin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/36Materials for grafts or prostheses or for coating grafts or prostheses containing ingredients of undetermined constitution or reaction products thereof, e.g. transplant tissue, natural bone, extracellular matrix
    • A61L27/38Materials for grafts or prostheses or for coating grafts or prostheses containing ingredients of undetermined constitution or reaction products thereof, e.g. transplant tissue, natural bone, extracellular matrix containing added animal cells
    • A61L27/3804Materials for grafts or prostheses or for coating grafts or prostheses containing ingredients of undetermined constitution or reaction products thereof, e.g. transplant tissue, natural bone, extracellular matrix containing added animal cells characterised by specific cells or progenitors thereof, e.g. fibroblasts, connective tissue cells, kidney cells
    • A61L27/3834Cells able to produce different cell types, e.g. hematopoietic stem cells, mesenchymal stem cells, marrow stromal cells, embryonic stem cells
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • A61L27/54Biologically active materials, e.g. therapeutic substances
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L27/00Materials for grafts or prostheses or for coating grafts or prostheses
    • A61L27/50Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
    • A61L27/58Materials at least partially resorbable by the body
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/40Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
    • A61L2300/412Tissue-regenerating or healing or proliferative agents
    • A61L2300/414Growth factors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS 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
    • A61L2430/00Materials or treatment for tissue regeneration
    • A61L2430/32Materials or treatment for tissue regeneration for nerve reconstruction

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Dermatology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Transplantation (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Cell Biology (AREA)
  • Molecular Biology (AREA)
  • Developmental Biology & Embryology (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Zoology (AREA)
  • Botany (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials For Medical Uses (AREA)

Abstract

The present invention relates to bioengineering field, be specifically related to a kind of rush CO2 laser weld pipe and preparation method thereof.In order to overcome the best problem of neurological functional recovery after current direct neural suture, the invention provides a kind of rush CO2 laser weld pipe.This CO2 laser weld pipe is the hollow pipe that the solution of the propylated gelatin of base is made.The growth that this rush CO2 laser weld pipe is neural provides a stable microenvironment.Be conducive to wound to recover, promote neural functional rehabilitation, close with nerve autograft function and be better than simple nerve trachea, there is good potential applicability in clinical practice.

Description

Promote CO2 laser weld pipe and preparation method thereof
Technical field
The present invention relates to biological engineering and biomedical sector, be specifically related to promote CO2 laser weld pipe and preparation method thereof.
Background technology
Current various wound such as compressing, drawing-off, tear, the reason such as cut-out causes neural part or all of damage, Thus nerve causes afunction and other nervous system diseasies.For there is the nerve of damage, neural neuron axon is suitable Can regenerate in the case of when.By the development of the most micro-neurosurgery of neurosurgery, the reparation of nerve injury and regeneration are It is possibly realized.Research at present and the CO2 laser weld technology applied clinically mainly have: directly stitching, neural transplantation (autotransplantation Or heteroplastic transplantation) and repair by promoting CO2 laser weld pipe.Directly it coincide and be only limited to shorter neurotmesis (less than 5mm), no Then can there is identical tension force, be unfavorable for neuranagenesis;Neural transplantation and rush CO2 laser weld pipe are mainly used in the long nerve blocked and repair Multiple, but neural transplantation owing to being limited by donor, immunoreation etc., it is difficult to commonly use;CO2 laser weld pipe can provide One good microenvironment promotes perineural reparation, has been obtained for large range of application in clinic.The most clinical What middle use was most is a kind of silica gel tube, it is possible to guide the nerve tract proximate growth from neurologic defect position.But face Bed result shows, owing to silica gel tube is that a kind of material that can not degrade needs second operation to take out, brings secondary nerve injury;Shape Shape is difficult to mate completely with the damage location of patient;And biological activity is relatively low;Can not obtain very compared to neural transplantation patient Good functional rehabilitation.
Summary of the invention
In order to solve the problems referred to above that this area exists, the invention provides a kind of rush CO2 laser weld pipe.
This rush CO2 laser weld pipe is that the solution of methyl-prop alkylene gelatin forms the hollow pipe that gel prepares.
Wherein, the tube wall of above-mentioned rush CO2 laser weld pipe is attached with fat stem cell.Fat it is attached with dry on described tube wall Cell refers to that at least side tube wall is attached with fat stem cell.
Further, above-mentioned rush CO2 laser weld pipe is to inject the solution of methyl-prop alkylene gelatin to promote CO2 laser weld pipe mold In prepare.
The present invention additionally provides the method that preparation promotees CO2 laser weld pipe simultaneously, it is characterised in that comprise the following steps:
A, the solution preparing methyl-prop alkylene gelatin respectively and rush CO2 laser weld pipe mold;
B, injecting in mould by the solution of methyl-prop alkylene gelatin, gel to be formed, mold removal, lyophilizing obtains promoting nerve Repair pipe;
C, fat stem cell suspension is added drop-wise to step b prepare promote CO2 laser weld pipe wall on, hatch in incubator 0.5h~1h, makes cell fully be attached on rush CO2 laser weld pipe, to obtain final product.
Wherein, the concentration of above-mentioned methyl-prop alkylene gelatin solution is 5%~10%w/v.
Further, in said method step b, before the solution of methyl-prop alkylene gelatin injects mould, over cure need to be added Acid ammonium to content is 0.1%~0.5%w/v and tetramethylethylenediamine is 0.05%~0.2%w/v to content, fully mixes To mixed solution.In Ben, the w/v in invention is the concentration measurement unit chemically commonly used, and refers to every milliliter of material added Quality, as 0.5% refers to that the solution of 1mL adds the amount of 5mg.
Wherein, in said method step b: the mixed solution obtained is injected rapidly and is placed into-20 DEG C~the mould of 0 DEG C In tool;After fully reaction forms gel, at thaw at RT, mold removal.
Wherein, the rush CO2 laser weld pipe that said method step b obtains after taking out mould need to carry out frozen dried.Above-mentioned freezes Dry-cure is to process to removing the moisture promoted in CO2 laser weld pipe.
Wherein, after said method step c is hatched in incubator, after neurocele adds culture medium, it is cultivated for 2~6 Hour obtain promoting CO2 laser weld pipe.
Wherein, the mould of above-mentioned rush CO2 laser weld pipe is to be printed the personalized rush CO2 laser weld pipe die indirectly prepared by 3D Tool or metal promote CO2 laser weld pipe mold indirectly.
Wherein, the concentration of the fat stem cell suspension described in said method is 1 × 107~1 × 108Individual/mL.
The above-mentioned rush CO2 laser weld pipe prepared.
The beneficial effects of the present invention is: the present invention, by indirect 3D technology, is prepared for a kind of degradable gelatin and derives Thing (GelMA) promotees CO2 laser weld pipe, and can add fat stem cell.Experiment shows, the rush CO2 laser weld of fat stem cell Pipe can directional guide nerve growth, reduce scar tissue and neuromatous growth, it is provided that the micro-loop that a nerve growth is good Border.The existence of fat stem cell can discharge rush nerve growth factor, accelerates perineural pattern and functional restoration.This Bright GelMA promotees CO2 laser weld pipe and has good biocompatibility and certain mechanical strength, elapses over time, promotees nerve Repair pipe can progressively decompose, it is to avoid neurocele is to neural follow-up compressing and causes inflammation, also avoids second operation, has very Good potential applicability in clinical practice.
Accompanying drawing illustrates:
Fig. 1, by 3-dimensional software (soildwork) and 3D printer be prepared for promote CO2 laser weld pipe mold.
Fig. 2, the Physico-Chemical Characterization of neurocele of preparation.A is prepared for promoting sciatic nerve according to the sciatic nerve of rat and repaiies Multiple pipe.B is scanning electron microscope (SEM) photograph;C external degradation under collagenase effect;The subcutaneous degraded in D and E 1-8 week and H&E figure.By The rush CO2 laser weld pipe that knowable to figure, we prepare is a kind of cavernous degradable biological material, and the biofacies having had Capacitive.
Fig. 3, to doing the dyeing (A) of Live/dead at the fat stem cell promoting to have cultivated 2 days on CO2 laser weld pipe, Luo Dan Bright phalloidin (B).C figure is the SEM figure after fat stem cell is cultivated 2 days in culture dish, and D figure is that fat stem cell exists Promoting the SEM figure after cultivating 2 days in CO2 laser weld pipe, E figure is calculated at culture dish by different time points and promotees CO2 laser weld pipe The vegetative state of middle cell.F figure and promotees to cultivate neurotrophy two days later in CO2 laser weld pipe at culture dish for fat stem cell The release conditions of the factor.As can be seen from the figure fat stem cell can grow in GelMA promotees CO2 laser weld pipe and breed. Fat stem cell secretory nerve trophic factors can be promoted promoting CO2 laser weld pipe.
2 after Fig. 4, different operation group, the sciatic nerve index of 4,8,16 weeks.Promote the addition of CO2 laser weld pipe as seen from the figure Be conducive to neurological functional recovery, and plus the functional restoration of energy accelerator nerve after fat stem cell.The explanation of this figure promotees nerve Repair pipe and can promote the functional restoration of nerve plus fat stem cell.
4 after Fig. 5, different operation group, the sciatic nerve speed of 8,16 weeks.Promote adding of CO2 laser weld pipe as seen from the figure Enter beneficially neurological functional recovery, and plus the functional restoration of energy accelerator nerve after fat stem cell.
Fig. 6, A and B perform the operation figure, produce 1cm on sciatic nerve, then connect rush CO2 laser weld pipe and (or promote nerve and repair Multiple pipe+fat stem cell), C, D, E, F are after 16 weeks, the audio-visual picture of neural recovery state.(C sham operated rats, D is for for certainly Somatic nerves is transplanted, and E is for promoting CO2 laser weld pipe, and F is for promoting CO2 laser weld pipe+fat stem cell group).
Fig. 7, A, B, C, D be respectively sham operated rats, nerve autograft group, promote CO2 laser weld pipe group, promote CO2 laser weld pipe+ The H&E figure of the gastrocnemius of fat stem cell group;E is the average diameter of the meat fiber of different group.F is experiment operation group and vacation The weight in wet base ratio of the gastrocnemius of operation group.
Detailed description of the invention:
The present invention, by indirect 3D technology, is prepared for a kind of degradable gelatine derivative (GelMA) and promotees CO2 laser weld pipe, Also can be nerve trachea, and fat stem cell can be added.
This CO2 laser weld pipe is that the solution of methyl-prop alkylene gelatin forms the hollow pipe that gel prepares.Above-mentioned rush CO2 laser weld Pipe promotees to prepare in CO2 laser weld pipe mold for being injected by the solution of methyl-prop alkylene gelatin.Wherein, this rush CO2 laser weld pipe is extremely Few side tube wall is attached with fat stem cell.
This preparation promotees CO2 laser weld pipe and specifically can be prepared as follows:
A, the solution preparing methyl-prop alkylene gelatin respectively and rush CO2 laser weld pipe mold;
B, injecting in mould by the solution of methyl-prop alkylene gelatin, gel to be formed, mold removal, lyophilizing obtains promoting nerve Repair pipe;
C, fat stem cell suspension is added drop-wise to step b prepare promote CO2 laser weld pipe wall on, hatch in incubator 0.5h~1h, makes cell fully be attached on rush CO2 laser weld pipe, to obtain final product.
The concentration of methyl-prop alkylene gelatin solution is that the intensity making formation gel properly and can drop in the suitable time Solve.The concentration of 5%~10%w/v disclosure satisfy that needs.
Further, in said method step b, before the solution of methyl-prop alkylene gelatin injects mould, over cure need to be added Acid ammonium and tetramethylethylenediamine, obtain mixed solution, injected rapidly in mould by the mixed solution obtained, and is formed solidifying with reaction Glue.The effect of APS is to produce free radical, makes the carbon-carbon double bond in GelMA react.And TEMED play promotion APS be produced from by Base, accelerates the effect of reaction.Mould is typically placed under-20 DEG C~0 DEG C of environment, after fully reacting formation gel, in room temperature solution Freeze, mold removal.
The rush CO2 laser weld pipe obtained after taking out mould preferably carries out frozen dried, removes as far as possible and promotees in CO2 laser weld pipe Moisture.
After step c is hatched in incubator, it is also possible to add culture medium on rush CO2 laser weld pipe, be cultivated for 2~6 hours Obtain cellularised rush CO2 laser weld pipe.This like cell adheres to more preferably on tube wall, and activity can be higher.
Preparation promotees the various conventional mould that the mould of CO2 laser weld pipe can be this area.Wherein, in order to use target Neural shapes more mates, and mould can be selected for being printed by 3D between the personalized rush CO2 laser weld pipe mold indirectly prepared or metal Connect rush CO2 laser weld pipe mold.
The concentration of the fat stem cell suspension used during preparation is typically adjusted to 1 × 107~1 × 108Individual/ml.
Additionally, present invention also offers the above-mentioned rush CO2 laser weld pipe prepared.
Below by way of detailed description of the invention, the present invention is carried out further description.
Embodiment one, structure promote CO2 laser weld pipe mold
Promote CO2 laser weld pipe mold by 3D printer Design and preparation, and then rush CO2 laser weld pipe can be prepared.
First rat sciatic nerve diameter is measured in this is tested, the rat sciatic nerve diameter of 200~250g About 1.2~1.3mm, it is contemplated that the factor such as neural swelling after peripheral nerve injury, for the rush god of Rats'Sciatic Nerve Injury customization Repaired pipe about internal diameter is 1.5mm, and catheter outer diameter is 4mm (pipe thickness is 1.25mm).Gone out by SolidWork software design And use desktop printer (TD ARTIST) print and promote the mould that CO2 laser weld pipe mates, see Fig. 1.
Embodiment two present invention promotees the preparation of CO2 laser weld pipe
1, the gelatin (GelMA) of methyl-prop alkylene is prepared
(1), at 60 DEG C, by complete with the concentration of 10% (W/V) for type A gelatin (purchased from Sigma company, article No.: G1890) It is dissolved in phosphate buffer (PBS);
(2), it is added dropwise over methacrylic anhydride so that it is concentration is 20% (v/v), fully reacts 1 hour at 50 DEG C;
(3), dilute with the PBS (40 DEG C) of 5 times of volumes to terminate above-mentioned reaction;
(4), product is dialysed 2 weeks at 40 DEG C, then lyophilizing in freeze dryer, preserve at-20 DEG C.
2, preparation personalization promotees CO2 laser weld pipe
(1), at 60 DEG C, being completely dissolved in distilled water by GelMA, make the solution of 5% (w/v), the solution of i.e. every 1mL is molten Solve 50mg GelMA;
(2), by the GelMA being completely dissolved it is placed in 5 minutes on ice, is subsequently adding Ammonium persulfate. (APS;Public purchased from Sigma Department) to 0.5% (w/v) and tetramethylethylenediamine (TEMED;Purchased from Sigma company) to 0.1% (w/v), fully mix;
(3), said mixture is injected rapidly in the mould being placed into-20 DEG C of refrigerators;
(4), frozen 24 hours, fully thaw, the effective distilled water of CO2 laser weld will be promoted after mold removal the most clean, then Lyophilizing also saves backup at-20 DEG C.
3, the sign of CO2 laser weld pipe is promoted
In aforementioned manners formation determination rat right sciatic nerves and design and be prepared for promote CO2 laser weld pipe, then to system Standby rush CO2 laser weld pipe carries out characterizing (result sees Fig. 3).
Result shows
(1), scanning electron microscope show that the rush CO2 laser weld pipe of preparation has pore structure, the size in hole about 167 ± 13.5um, porosity 89.3% ± 1.04%, swelling ratio 9.47 ± 1.00;
(2) by being placed on promoting CO2 laser weld pipe in the Type Ⅱ collagen enzyme of 1mg/mL, by neural at different time points The quality of pipe compares with the quality of original neurocele, finds to promote CO2 laser weld pipe the most about 20 hours degradable.So After will to promote CO2 laser weld pipe heeling-in subcutaneous at rat back, at different time points by the H&E picture at heeling-in position and naked eyes Observe, find that promoting the CO2 laser weld pipe the most degradable time is 2~4 months.
(3), the rush CO2 laser weld pipe heeling-in dorsal sc to rat of fat stem cell will not be added, 1,2,4,8 The neurocele taking off heeling-in week does H&E dyeing, and result shows, the surrounding promoting CO2 laser weld pipe only has a small amount of inflammatory cell. Illustrate that the inflammatory reaction that this rush CO2 laser weld pipe causes is less, there is good histocompatibility.
4, cellularised rush CO2 laser weld pipe is prepared
On the basis of above-mentioned steps 3, the present invention attempts promoting to adhere on CO2 laser weld pipe fat stem cell, adhering mode Using new mode, and the mode of dropping prepares cellularised rush CO2 laser weld pipe, result sees Fig. 4.
Concretely comprise the following steps:
(1), from rat groin fatty tissue isolated fat stem cell, complete medium (DMEM low sugar+ 10% hyclone) middle cultivation so that it is external abundant amplification;
(2), gather in the crops fat stem cell, take the rush CO2 laser weld pipe prepared before part, promote CO2 laser weld pipe at each Upper dropping 30 μ l is altogether containing 1 × 106The cell suspension of fat stem cell is hatched 1 hour in incubator, makes cell fully be attached to Promote on CO2 laser weld pipe;
(3), it is further continued for cultivating completely 3 hours by the rush CO2 laser weld pipe containing fat stem cell, uses pipettor to add The DMEM fluid medium (comprising the hyclone of 10%, buy in Invitrogen company) of 500uL, makes fat stem cell fill Divide and attach growth, obtain cellularised rush CO2 laser weld pipe.
Embodiment three, the present invention promote the vivo efficacy test of CO2 laser weld pipe
Choose adult rat (body weight 200~250g) and build model, assess rush CO2 laser weld pipe and repair peripheral nerve.
Rat is divided into 4 groups and accepts functional assessment, respectively sham operated rats, nerve autograft group, rush CO2 laser weld pipe Group, rush CO2 laser weld pipe+fat stem cell group.
Operation technique is anaesthetized for rat is carried out lumbar injection chloral hydrate (0.5 milliliter/100 grams).After rat Body hair is removed, and cuts 1 millimeter of wound parallel with femur, separated by biceps brachii m., expose sciatic nerve, hands at sciatic nerve Art position is about at distance furcal nerve 5mm.
Sham operated rats does not cut off nerve;Nerve autograft group is for cutting off seam respectively at distance furcal nerve 5mm~15mm Close;Promote CO2 laser weld Guan Zuwei and at distance furcal nerve 5mm~15mm, cut off the nerve of 1cm, then by fat-free stem cell Rush CO2 laser weld pipe seam be combined in two ends;Promoting CO2 laser weld pipe+fat stem cell group is at distance furcal nerve 5mm~15mm Cut off the nerve of 1cm, be then combined in two ends by having added the rush CO2 laser weld pipe seam being attached with fat stem cell.
By histology, sciatic nerve index, the mode such as electro physiology detects each group of index, result see Fig. 4~Fig. 7 and Accompanying drawing explanation.By interpretation, prolongation over time, the rat of fat stem cell+rush CO2 laser weld pipe is used to exist The sciatic nerve index of functional assessment and nerve conduction velocity all become closer to nerve autograft group, and this rush nerve is described Repair pipe and there is in zoopery preferable result, have good application prospect clinically.

Claims (10)

1. promote CO2 laser weld pipe, it is characterised in that be to be formed, by the solution of methyl-prop alkylene gelatin, the hollow pipe that gel prepares.
Rush CO2 laser weld pipe the most according to claim 1, it is characterised in that: it is attached with fat stem cell on tube wall.
Rush CO2 laser weld pipe the most according to claim 1, it is characterised in that: for the gelatin solution of methyl-prop alkylene is injected Promote CO2 laser weld pipe mold prepares.
4. the method promoting CO2 laser weld pipe described in preparation any one of claims 1 to 3, it is characterised in that comprise the following steps:
A, the solution preparing methyl-prop alkylene gelatin respectively and rush CO2 laser weld pipe mold;
B, injecting in mould by the solution of methyl-prop alkylene gelatin, gel to be formed, mold removal, lyophilizing obtains promoting CO2 laser weld Pipe;
C, fat stem cell suspension is added drop-wise to step b prepare promote CO2 laser weld pipe wall on, hatch in incubator 0.5h~ 1h, makes cell fully be attached on rush CO2 laser weld pipe, obtains cellularised rush CO2 laser weld pipe.
Method the most according to claim 4, it is characterised in that: the concentration of the solution of described methyl-prop alkylene gelatin is 5%~10%w/v.
Method the most according to claim 4, it is characterised in that: in the method for described step b, at methyl-prop alkylene gelatin Solution injects before mould, and need to add Ammonium persulfate. to content is 0.1%~0.5%w/v and tetramethylethylenediamine is to content 0.05%~0.2%w/v, fully it is uniformly mixed so as to obtain mixed solution.
Method the most according to claim 6, it is characterised in that: the mixed solution obtained is injected rapidly be placed into- In the mould of 20 DEG C~0 DEG C;After fully reaction forms gel, at thaw at RT, mold removal.
Method the most according to claim 4, it is characterised in that: after described step c is hatched in incubator, outside neurocele Face adds culture medium, is cultivated for 2~6 hours obtaining promoting CO2 laser weld pipe, and cultivation below is to cultivate in incubator.
Method the most according to claim 4, it is characterised in that: the concentration of described fat stem cell suspension is 1 × 107~1 ×108Individual/mL.
10. the rush CO2 laser weld pipe prepared by the method described in any one of claim 4~7.
CN201610729307.4A 2016-08-26 2016-08-26 Promote CO2 laser weld pipe and preparation method thereof Pending CN106237382A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610729307.4A CN106237382A (en) 2016-08-26 2016-08-26 Promote CO2 laser weld pipe and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610729307.4A CN106237382A (en) 2016-08-26 2016-08-26 Promote CO2 laser weld pipe and preparation method thereof

Publications (1)

Publication Number Publication Date
CN106237382A true CN106237382A (en) 2016-12-21

Family

ID=57596271

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610729307.4A Pending CN106237382A (en) 2016-08-26 2016-08-26 Promote CO2 laser weld pipe and preparation method thereof

Country Status (1)

Country Link
CN (1) CN106237382A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106729983A (en) * 2016-12-30 2017-05-31 四川大学 One kind promotees CO2 laser weld composite conduit and preparation method thereof
CN109395165A (en) * 2018-12-21 2019-03-01 江阴司特易生物技术有限公司 A kind of artificial composite nerve conduit and preparation method
CN115137884A (en) * 2022-06-28 2022-10-04 中国科学院苏州生物医学工程技术研究所 Injectable hydrogel for nerve injury repair and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1580253A (en) * 2004-05-18 2005-02-16 中山大学附属第一医院 Tissue engineered peripheral nerve graft
CN1872354A (en) * 2006-03-31 2006-12-06 锦州医学院附属第一医院 Duct filler material in use for bridge grafting nerves, and preparation method
CN102688110A (en) * 2012-06-13 2012-09-26 北京天新福医疗器材有限公司 Multi-aperture nerve repairing tube and preparation method and application thereof
CN105412985A (en) * 2016-01-22 2016-03-23 江苏省人民医院 Preparation technology of novel nerve conduit
CN105879112A (en) * 2016-04-21 2016-08-24 四川大学 Neural restoration promoting tube as well as preparation method and application thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1580253A (en) * 2004-05-18 2005-02-16 中山大学附属第一医院 Tissue engineered peripheral nerve graft
CN1872354A (en) * 2006-03-31 2006-12-06 锦州医学院附属第一医院 Duct filler material in use for bridge grafting nerves, and preparation method
CN102688110A (en) * 2012-06-13 2012-09-26 北京天新福医疗器材有限公司 Multi-aperture nerve repairing tube and preparation method and application thereof
CN105412985A (en) * 2016-01-22 2016-03-23 江苏省人民医院 Preparation technology of novel nerve conduit
CN105879112A (en) * 2016-04-21 2016-08-24 四川大学 Neural restoration promoting tube as well as preparation method and application thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106729983A (en) * 2016-12-30 2017-05-31 四川大学 One kind promotees CO2 laser weld composite conduit and preparation method thereof
CN109395165A (en) * 2018-12-21 2019-03-01 江阴司特易生物技术有限公司 A kind of artificial composite nerve conduit and preparation method
CN115137884A (en) * 2022-06-28 2022-10-04 中国科学院苏州生物医学工程技术研究所 Injectable hydrogel for nerve injury repair and preparation method thereof

Similar Documents

Publication Publication Date Title
EP1076533B1 (en) Guided development and support of hydrogel-cell compositions
EP0863776B1 (en) A biologic material comprising an efficient culture of bone marrow stem cells partially or completely differentiated into connective tissue cells and a three-dimensional biocompatible and biodegradable matrix consisting of a hyaluronic acid derivative
Zimmermann et al. Cardiac tissue engineering for replacement therapy
EP1747264B1 (en) Multicellular tissue and organ culture systems
US9592255B2 (en) Scaffold-free three dimensional nerve fibroblast constructs
US8709081B2 (en) Cellular scaffold
CA2141851A1 (en) Production of graft tissue from extracellular matrix
JPH10513363A (en) Submucosal tissue as a growth substrate for cells
US20070286880A1 (en) Inoculated spongiform scaffold for transplantation and tissue regeneration
DE69803065T2 (en) CELL CULTURE MATRIX AND BIODEGRADABLE THREE-DIMENSIONAL MATRIX ON A HYALURONIC ACID DERIVATIVE BASE
CN113846050B (en) Preparation method of tissue organoids
CN106237382A (en) Promote CO2 laser weld pipe and preparation method thereof
KR20140033057A (en) Cell-synthesized particles
AU2007219520B2 (en) Prevascularized tissue transplant constructs for the reconstruction of a human or animal organ
CA2419923C (en) Vascularised tissue graft
JP2007528252A (en) Autogenesis bioscaffolding and tissue matrix; methods and uses thereof
CN115747132A (en) Porous scaffold comprising plant protein and cultured meat prepared therefrom
CN101195044A (en) Tissue engineered fine particle tissue and method for preparing the same
EP1885844B1 (en) Preparation and use of basement membrane particles
JP3603103B2 (en) Co-culture carrier for fertilized eggs of animals (excluding humans) and method for culturing fertilized eggs of animals (excluding humans) using this carrier
KR20220136936A (en) Tissue-derived extracelluar matrix derivatives modified with phenol derivatives for fabrication of artificial tissue
CN117551604A (en) Repair of endometrial lesions with decellularized amniotic scaffold complexes carrying endometrial mesenchymal stem cells and epithelial organoids
DE102004025081B4 (en) Multicellular tissue and organ culture systems
AU2006254703A1 (en) Preparation and use of basement membrane particles

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20161221

RJ01 Rejection of invention patent application after publication