CN101574539B - Gelatin sponge and preparation method thereof - Google Patents

Gelatin sponge and preparation method thereof Download PDF

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Publication number
CN101574539B
CN101574539B CN2009100872748A CN200910087274A CN101574539B CN 101574539 B CN101574539 B CN 101574539B CN 2009100872748 A CN2009100872748 A CN 2009100872748A CN 200910087274 A CN200910087274 A CN 200910087274A CN 101574539 B CN101574539 B CN 101574539B
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gelfoam
gelatin
aqueous
crosslinking
hydrogel
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CN101574539A (en
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许零
杨超
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Xiamen Lingfu Biotechnology Co ltd
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Peking University
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Abstract

The invention provides gelatin sponge, gelatin aqueous solution is irradiated to crosslink to form gelatin hydrogel, and then the gelatin hydrogel is swollen, frozen and dried to obtain the gelatin sponge. The invention also provides a preparation method of the gelatin sponge by an irradiation crosslinking way, the whole process flow is finished in a pure water system, the irradiation and crosslinking processes have sterilizing function and good controllability, the obtained product has better structural uniformity compared with a chemical crosslinking method, and the gelatin sponge has uniqueadvantages as biomedical materials.

Description

A kind of gelfoam and preparation method thereof
Technical field
The present invention relates to a kind of gelfoam and preparation method thereof, specifically, relate to a kind of gelfoam that adopts the preparation of crosslinking with radiation method.
Background technology
Gelatin has good biological activity, has purposes extremely widely at biomedical sector.Gelfoam has very strong anastalsis, but a large amount of moisture and the transudates of fast Absorption can be used as the dressing of operative incision, various wound surface, and the suppository of various interventional therapys.Use chitin modified gelfoam, then can further improve the anthemorrhagic speed of sponge, the ability of absorption transudate, and can improve the pliability of sponge.
Mostly traditional gelfoam or gelatine-chitosan sponge are with hydrochloric acid, acetate dissolution chitosan, make gelatin or gelatin/chitosan mixed liquor crosslinked with cross-linking agent such as formaldehyde, glutaraldehydes, obtain foam product with freeze-drying dehydration, sterilization at last.But a large amount of cytotoxic materials have been used in these technologies; As: hydrochloric acid, acetic acid, formaldehyde, glutaraldehyde etc.; Sterilization process adopts epoxyethane fumigation mostly, and the residual toxicity of these chemical agents can have a strong impact on cell growth and tissue regeneration, thereby influences therapeutic effect.
Chinese invention patent CN1097980A provides a kind of method for preparing of chitose-gelatine sponge, is intended to make adhesive bandage, hemostasis subsides.This invention is gelatin, chitosan, hydrochloric acid, sodium hydroxide, formaldehyde, distilled water wiring solution-forming, through get blisters, freezing, dry, sterilize and to process mandruka.But the very big chemical reagent of cytotoxicity such as formaldehyde, hydrochloric acid, sodium hydroxide have been used in this technology; Sterilization process adopts epoxyethane fumigation; These technologies are gradually by relevant regulation limitations or ban use of, and are very poor as the biological safety that adhesive bandage, hemostasis are pasted.
Chinese invention patent CN1775302A provides a kind of method for preparing of chitose-gelatine sponge wound dressing.This invention is with dilute hydrochloric acid, acetic acid, formic acid solution dissolving chitosan; Gelatin is used water dissolution; Add materials such as plasticizers such as cross-linking agent, glycerol, Margarita powder such as formaldehyde or Biformyl, after these components are mixed, obtain the spongy wound dressing of 1-2 millimeters thick with freeze-drying.But this technology has used formaldehyde, Biformyl, hydrochloric acid, acetic acid, formic acid etc. that the chemical reagent of bio-toxicity is arranged equally, and has used the Margarita powder of nonbiodegradability, and its granule possibly remain in the wound tissue, becomes foreign body in vivo.
It is the technology of feedstock production absorbable gelatin sponge particle suppository with the gelatin that Chinese invention patent CN101161298A provides a kind of.This is invented after aqueous gelatin solution and the formalin mixing, the freezing crosslinked porous spongy sample that obtains.Thaw after scouring, drying of spongy sample obtained gelfoam.Gelfoam is freezing, pulverize, screening obtains absorbable gelatin sponge particle suppository.This invention uses formaldehyde to make cross-linking agent, though washing step is arranged, the reagent in the porous material is difficult to eliminate through simple washing, and the formaldehyde residue problem can influence the histocompatibility of end article inevitably.
The present invention is intended to adopt green synthesis process, obtains that biocompatibility is better, the better gelfoam of structural homogeneity.
Summary of the invention
The present invention is intended to abandon the traditional handicraft of using a large amount of poisonous chemical agents, and a kind of gelfoam that adopts the crosslinking with radiation method to obtain is provided, and its good biocompatibility, structural homogeneity are good.
Another object of the present invention is to provide a kind of method for preparing of gelfoam, this method adopts crosslinking with radiation and radiation sterilization to carry out simultaneously, can obtain that biocompatibility is better, the better gelfoam of structural homogeneity.
The object of the invention and solve its technical problem and adopt following technical scheme to realize.
A kind of gelfoam of the present invention, it becomes gelatin hydrogel through earlier aqueous gelatin solution being carried out crosslinking with radiation, carries out swelling then, lyophilization forms.
Described crosslinking with radiation adopts cobalt-60 or electron beam to carry out crosslinking with radiation, and irradiation is 1~50kGy, is preferably 10~30kGy.
The concentration expressed in percentage by weight of said aqueous gelatin solution is 3~50%, is preferably 10~30%.
Also can contain water-soluble natural in the said aqueous gelatin solution and gather polysaccharide.The ratio that gelatin and water-soluble natural gather polysaccharide is 10: 0~1: 9, is preferably 4: 6~8: 2.
Described water-soluble natural gathers polysaccharide and is selected from Aloe polysaccharide, carboxymethyl chitosan, hydroxypropyl chitosan, sodium alginate, propylene glycol alginate, sodium carboxymethyl cellulose, hydroxypropyl emthylcellulose, the carboxymethyl hydroxypropyl cellulose one or more.
The swelling of said gelatin hydrogel is through carrying out in the pharmaceutical aqueous solution that is immersed in sterilized water, somatomedin aqueous solution or auxiliary treatment.Swelling time is 2~72 hours, is preferably 6~24 hours.Swelling process carries out in sterilizing room.
Said somatomedin aqueous solution can select fibroblast growth factor that those skilled in the art use always or hEGF etc. can promote the somatomedin aqueous solution that skin tissue regeneration is repaired.
Can select pharmaceutical aqueous solutions such as this area disinfectant commonly used, antibiotic, burn-scald medicine, Pletaal for pharmaceutical aqueous solution, make it to have corresponding auxiliary treatment effect, its consumption can adopt this area conventional amount used.
The gelatin hydrogel degree of cross linking through the present invention preparation is in 70~99% scopes, and water absorption rate is adjustable in 5~500 times of scopes.
The method for preparing of gelfoam of the present invention, it carries out crosslinking with radiation to aqueous gelatin solution earlier and becomes gelatin hydrogel, carries out swelling, lyophilization then.
Said cryodesiccated temperature is at-10~-80 ℃, preferred-20~-60 ℃.
Adopt the good porous gelfoam of crosslinking with radiation method availability of the present invention.The aperture has excellent absorptive tissue liquid and hemostatic capability, preferred 20~70 micrometer ranges in 5~100 microns scope.
If necessary, can the porous gelfoam is freezing, pulverize, screening, obtain the graininess gelfoam of different-grain diameter.
Through the gelfoam that the present invention obtains, can be used as bleeding-stopping dressing, burn wound dressing, ulcer dressing etc.; Absorbable gelatin sponge particle can be used as suppository and is used for various interventional therapys, like artery embolization for treatment of hysteromyoma, hemangioma, arteriovenous malformotion, malignant tumor and various massive hemorrhage etc.
The gelfoam that utilizes method provided by the invention to obtain does not have chemical agent residual, has better biocompatibility and structural homogeneity.Fibroblast growing state on gelatin/carboxymethyl chitosan hydrogel of the present invention is good, and the rate of increase was greater than 100% in 5 days; And on the hydrogel of acetic acid dissolving Preparation of Chitosan culturing fibroblasts, 7 days rates of increase are between 82~97%; Do not find cell culture data, but formaldehyde toxicity is higher than acetic acid, estimates that its cell proliferation rate is lower with formaldehyde crosslinking gelatin and/or chitosan gel rubber material.
Gelfoam of the present invention and radiation method for preparing thereof have advantage and beneficial effect at least:
(1) the present invention adopts water-soluble natural to gather polysaccharide to replace chitosan, so solvent has substituted the material that acetic acid, formic acid etc. have skin irritation by water.
(2) water-soluble natural gathers polysaccharide and compares with chitosan, has the ability of better promotion tissue growth.
(3) gather polysaccharide-modified gelatin with water-soluble natural, can increase the water solublity and the pliability of gelatin, and can promote the granulation growth, use very crucial as dressing it.
(4) replace crosslinking technologicals such as formaldehyde, glutaraldehyde with the crosslinking with radiation technology generation, can avoid the chemical residual toxicity of product, play the effect of sterilization simultaneously.
(5) porous material that obtains with the crosslinking with radiation technology has better structural homogeneity, helps the adhesion and the skin tissue regeneration of skin tissue cell.
(6) controllability of this process is fine, and the structural homogeneity that obtains product is good than chemical crosslink technique also, has special advantages as bio-medical material.
The specific embodiment
Following examples are used to explain the present invention, but are not used for limiting scope of the present invention.
Embodiment 1
30 gram gelatin are dissolved in the 70 gram water, are heated to 80 ℃, stir, obtain 30% aqueous gelatin solution.Pour aqueous gelatin solution into plate,, obtain the degree of cross linking and be 99% gelatin hydrogel with cobalt-60 irradiation 20kGy.Hydrogel is soaked 24 hours to swelling equilibrium in sterilized water, obtain water absorption rate and be 10 times moisture porous material.Moisture porous material-80 ℃ of lyophilizations, with the classification of Universalpulverizer crushing screening, is obtained aperture and epigranular (average pore size is at 15 microns), the soft gelfoam embolization agent of quality under-20 ℃ of low temperature.
Embodiment 2
12 gram gelatin and 3 gram carboxymethyl chitosans are dissolved in the 85 gram water, are heated to 60 ℃, stir, obtain solid content and be 15% aqueous solution with the deaeration blender.Pour aqueous solution into plate,, obtain the degree of cross linking and be gelatin/carboxymethyl chitosan hydrogel of 82% with cobalt-60 irradiation 30kGy.Hydrogel is soaked 72 hours to swelling equilibrium in containing the aqueous solution of somatomedin, obtain water absorption rate and be 20 times moisture porous material.Moisture porous material-40 ℃ of lyophilizations, and is obtained aperture evenly (average pore size is at 50 microns), the soft gelatin/carboxymerhyl chitosan sponge dressing of quality.
Embodiment 3
4 gram gelatin and 6 gram hydroxypropyl chitosans are dissolved in the 90 gram water, are heated to 60 ℃, stir, obtain solid content and be 10% aqueous solution with the deaeration blender.Pour aqueous solution into plate,, obtain the degree of cross linking and be gelatin/hydroxypropyl chitosan hydrogel of 72% with cobalt-60 irradiation 10kGy.Hydrogel is soaked 36 hours to swelling equilibrium in sterilized water, obtain water absorption rate and be 90 times moisture porous material.Moisture porous material-40 ℃ of lyophilizations, is obtained aperture evenly (average pore size is at 80 microns), the soft gelatin/hydroxypropyl chitosan sponge dressing of quality.
Embodiment 4
8 gram gelatin and 12 gram propylene glycol alginates are dissolved in the 80 gram water, are heated to 60 ℃, stir, obtain solid content and be 20% aqueous solution with the deaeration blender.Pour aqueous solution into plate,, obtain the degree of cross linking and be gelatin/propylene glycol alginate hydrogel of 70% with cobalt-60 irradiation 50kGy.Hydrogel is soaked 48 hours to swelling equilibrium in the sterilized water that contains the 1mg/L basic fibroblast growth factor, obtain water absorption rate and be 220 times moisture porous material.Moisture porous material-80 ℃ of lyophilizations, is obtained aperture evenly (average pore size is at 30 microns), the soft gelatin/propylene glycol alginate sponge dressing of quality.
Embodiment 5
10 gram gelatin are dissolved in the 90 gram water, are heated to 80 ℃, stir, obtain 10% aqueous gelatin solution.Pour aqueous gelatin solution into plate,, obtain the degree of cross linking and be 90% gelatin hydrogel with cobalt-60 irradiation 5kGy.Hydrogel is soaked 6 hours to swelling equilibrium in the aseptic aqueous solution that contains 10% mannitol embolism resistance medicament, obtain water absorption rate and be 50 times moisture porous material.Moisture porous material-60 ℃ of lyophilizations, with the classification of Universalpulverizer crushing screening, is obtained aperture (average pore size is at 40 microns) and epigranular, the soft gelfoam embolization agent of quality under-20 ℃ of low temperature.
During as dressing, the capacity of absorptive tissue liquid and speed, anthemorrhagic speed are superior to commercially available gelfoam matched group with the gelfoam of method provided by the present invention preparation; During as sthptic sponge, the bleeding stopping period and the rate of always losing blood all are superior to matched group; During as suppository, biocompatibility and immunogenicity are superior to matched group.
Though, the present invention has been done detailed description in the preceding text with general explanation and specific embodiments, on basis of the present invention, can to some modifications of do or improvement, this will be apparent to those skilled in the art.Therefore, these modifications or the improvement on the basis of not departing from spirit of the present invention, made all belong to the scope that requirement of the present invention is protected.

Claims (12)

1. a gelfoam is characterized in that, it becomes gelatin hydrogel through earlier aqueous gelatin solution being carried out crosslinking with radiation, carries out swelling then, lyophilization forms.
2. gelfoam according to claim 1 is characterized in that, described crosslinking with radiation adopts cobalt-60 or electron beam to carry out crosslinking with radiation, and irradiation is 1~50kGy.
3. gelfoam according to claim 1 is characterized in that, the said gelatin hydrogel degree of cross linking is in 70~99% scopes.
4. according to any described gelfoam of claim 1-3, it is characterized in that the concentration expressed in percentage by weight of said aqueous gelatin solution is 3~50%.
5. gelfoam according to claim 4 is characterized in that, the concentration expressed in percentage by weight of said aqueous gelatin solution is 10~30%.
6. according to any described gelfoam of claim 1-3, it is characterized in that, also contain water-soluble natural in the said aqueous gelatin solution and gather polysaccharide.
7. gelfoam according to claim 6; It is characterized in that described natural polysaccharide is selected from one or more in Aloe polysaccharide, sodium alginate, propylene glycol alginate, sodium carboxymethyl cellulose, hydroxypropyl emthylcellulose, the carboxymethyl hydroxypropyl cellulose.
8. gelfoam according to claim 6 is characterized in that, the ratio that said gelatin and said water-soluble natural gather polysaccharide is 4: 6~8: 2.
9. according to any described gelfoam of claim 1-3, it is characterized in that the swelling of said gelatin hydrogel is carried out through being immersed in sterilized water, somatomedin aqueous solution or the adjuvant therapy medicaments aqueous solution.
10. prepare the method for any said gelfoam of claim 1-9, it is characterized in that, it carries out crosslinking with radiation to aqueous gelatin solution earlier and processes gelatin hydrogel, carries out swelling, lyophilization then.
11. the method for preparing according to the said gelfoam of claim 10 is characterized in that, said cryodesiccated temperature is at-10~-80 ℃.
12. the method for preparing according to the said gelfoam of claim 11 is characterized in that, said cryodesiccated temperature is at-20~-60 ℃.
CN2009100872748A 2009-06-15 2009-06-15 Gelatin sponge and preparation method thereof Expired - Fee Related CN101574539B (en)

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