Three-dimensional porous tissue engineering stand material and preparation thereof

A tissue engineering scaffold and three-dimensional porous technology, applied in the field of biomedical materials-tissue engineering scaffold materials, can solve the problems of natural polymers lacking spatial structure and mechanical strength, and unsatisfactory biodegradability, etc., to achieve good biological activity and degradation Sexuality, low cost, and wide-ranging effects

Inactive Publication Date: 2005-05-11
XIAMEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, a variety of materials have been used as bioscaffold materials, such as biopolymer materials, bioceramics/glass, etc., but most of these materials have different shortcomings, and it is difficult to fully meet the requirements of clinical applications.
For example, synthetic polymers (such as PLA, etc.) will have a chronic reaction with the body, and aseptic inf

Method used

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  • Three-dimensional porous tissue engineering stand material and preparation thereof
  • Three-dimensional porous tissue engineering stand material and preparation thereof
  • Three-dimensional porous tissue engineering stand material and preparation thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] With 1M acetic acid solution preparation concentration is that the gelatin solution of 15% and the chitosan solution that concentration is 1%, then by 1: 1 it is uniformly blended, and obtaining gelatin, chitosan content are respectively (by mass) 7.5%, 0.5% gelatin / chitosan mixed solution. Add GPSM and calcium nitrate to the above solution respectively, wherein GPSM / calcium nitrate is (by mass) 1 / 0.05; GPSM / (gelatin+chitosan) is (by mass) 0.5 / 1. The above solution was fully mixed for 4 hours at 40°C until it was completely uniform (no phase separation), and then 25ml of it was injected into a 5cm×8cm mold, sealed, and placed in a thermostat at 40°C for 3 days to obtain gelatin-chitopolymer Sugar-calcium silicate gel. Add 10 ml of 1M ammonia solution to the above-mentioned mold, let it stand at 25° C. for 16 hours, and then fully wash it with 1M NaCl solution and distilled water until neutral. Pre-freeze the ammonia-treated gel at -20°C for 24 hours, and then freeze-d...

Embodiment 2

[0047] Use 0.1M hydrochloric acid solution to prepare a gelatin solution with a concentration of 10%, add GPSM and calcium nitrate to the above solution respectively, wherein GPSM / calcium nitrate is (by quality) 1 / 0.05; GPSM / gelatin is (by quality) 0.5 / 1 . The above solution was fully mixed at 40°C for 4 hours until it was completely uniform (no phase separation), and then 25ml of it was injected into a 5cm×8cm mold, sealed, and placed in a thermostat at 40°C for 3 days to obtain gelatin-silicic acid calcium gel. Add 10 ml of 1M ammonia solution to the above-mentioned mold, let it stand at 25° C. for 16 hours, and then fully wash it with 1M NaCl solution and distilled water until neutral. The ammonia-treated gel was pre-frozen at -20°C for 24 hours, and then freeze-dried at -40°C at 5KPa for more than 48 hours. After freeze-drying, a gelatin-calcium silicate three-dimensional porous scaffold could be obtained. The porosity of the obtained porous material was tested by the Ar...

Embodiment 3

[0049] With 1M acetic acid solution preparation concentration is that the gelatin solution of 15% and the chitosan solution that concentration is 1%, then by 1: 1 it is uniformly blended, and obtaining gelatin, chitosan content are respectively (by mass) 7.5%, 0.5% gelatin / chitosan mixed solution. Add GPSM and calcium nitrate to the above solution respectively, wherein GPSM / calcium nitrate is (by mass) 1 / 0.05; GPSM / (gelatin+chitosan) is (by mass) 0.5 / 1. The above solution was fully mixed for 4 hours at 40°C until it was completely uniform (no phase separation), and then 25ml of it was injected into a 5cm×8cm mold, sealed, and placed in a thermostat at 40°C for 3 days to obtain gelatin-chitopolymer Sugar-calcium silicate gel. Add 10 ml of 1M ammonia solution to the above-mentioned mold, let it stand at 25° C. for 16 hours, and then fully wash it with 1M NaCl solution and distilled water until neutral. Pre-freeze the ammonia-treated gel in liquid nitrogen (-196°C) for 2 hours,...

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Abstract

A 3D porous scaffold material for tissue engineering to induce the generation of bone tissue is prepared from chitosan, gelatin, GPSM and calcium nitrate through sol-gel process, chemical treating and freeze drying. Its advantages are high bioactivity and degradability, proper porosity and pore diameter, and controllable properties.

Description

technical field [0001] The invention relates to a biomedical material with good biological activity and degradability-tissue engineering scaffold material. Background technique [0002] Since the 19th century, bone grafting has been committed to repairing large-scale bone defects caused by trauma, tumors, and infections to restore limb function. But there are many problems with this method, such as immune rejection and shortage of donor tissues and organs. An ideal strategy is to artificially cultivate tissues and organs, and then put forward the concept of tissue engineering, whose goal is to use the composite culture of cells and biological scaffold materials to regenerate bone tissue and achieve the purpose of repair. Among them, on the one hand, the scaffold material serves as a carrier of signal molecules or cells to deliver them to the defect site, and on the other hand, it provides a scaffold for new bone growth. At present, a variety of materials have been used as ...

Claims

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Application Information

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IPC IPC(8): A61L27/44A61L27/50A61L27/54A61L27/56A61L27/58
Inventor 任磊张其清
Owner XIAMEN UNIV
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