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首页> 外文期刊>Journal of materials science >Effect of enzymatic degradation of chitosan in polyhydroxybutyrate/chitosan/calcium phosphate composites on in vitro osteoblast response
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Effect of enzymatic degradation of chitosan in polyhydroxybutyrate/chitosan/calcium phosphate composites on in vitro osteoblast response

机译:聚羟基丁酸酯/壳聚糖/磷酸钙复合材料中壳聚糖的酶促降解对体外成骨细胞反应的影响

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Polyhydroxybutyrate/chitosan/calcium phosphate composites are interesting biomaterials for utilization in regenerative medicine and they may by applied in reconstruction of deeper subchondral defects. Insufficient informations were found in recent papers about the influence of lysozyme degradation of chitosan in calcium phosphate/chitosan based composites on in vitro cytotoxicity and proliferation activity of osteoblasts. The effect of enzymatic chitosan degradation on osteoblasts proliferation was studied on composite films in which the porosity of origin 3D scaffolds was eliminated and the surface texture was modified. The significantly enhanced proliferation activity with faster population growth of osteoblasts were found on enzymatically degraded biopolymer composite films with alpha-tricalcium phosphate and nanohydroxyapatite. No cytotoxicity of composite films prepared from lysozyme degraded scaffolds containing a large fraction of low molecular weight chitosans (LMWC), was revealed after 10 days of cultivation. Contrary to above in the higher cytotoxicity origin untreated nanohydroxyapatite films and porous composite scaffolds. The results showed that the synergistic effect of surface distribution, morphology of nanohydroxyapatite particles, microtopography and the presence of LMWC due to chitosan degradation in composite films were responsible for compensation of the cytotoxicity of nanohydroxyapatite composite films or porous composite scaffolds.
机译:聚羟基丁酸酯/壳聚糖/磷酸钙复合材料是用于再生医学的有趣的生物材料,它们可用于重建更深的软骨下缺损。在最近的论文中,关于磷酸钙/壳聚糖基复合物中壳聚糖的溶菌酶降解对成骨细胞体外细胞毒性和增殖活性的影响的信息不足。在复合膜上研究了酶促壳聚糖降解对成骨细胞增殖的影响,该复合膜消除了原始3D支架的多孔性并修饰了表面纹理。在具有α-磷酸三钙和纳米羟基磷灰石的酶降解的生物聚合物复合膜上,发现成骨细胞的增殖活性随着成骨细胞的快速增长而显着增强。培养10天后,未发现由含有大量低分子量壳聚糖(LMWC)的溶菌酶降解支架制备的复合膜的细胞毒性。与上述相反,较高的细胞毒性起源于未处理的纳米羟基磷灰石薄膜和多孔复合支架。结果表明,表面分布,纳米羟基磷灰石颗粒的形貌,微观形貌和复合壳聚糖降解引起的LMWC的协同作用是补偿纳米羟基磷灰石复合膜或多孔复合支架的细胞毒性的原因。

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