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Biosafety evaluation of a biodegradable gelatin hydrogel wound dressing for the delivery of growth factors

机译:可生物降解的明胶水凝胶伤口敷料对生长因子的递送的生物安全性评估。

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Although traditional wound dressings (nonocclusive) offering dry wound healing conditions still account for the largest segment of the dressing market, the use of occlusive dressings, hydrocolloid and hydrogel dressings which offer moist wound healing conditions has increased significantly. A next important step in the development of new dressings is the introduction of medicated wound dressings capable of delivering active substances to the wound site. For instance, it is known that exogenous growth factor applications into the wound site enhances wound repair. Gelatin hydrogels cross-linked by dextran dialdehydes have been shown to allow the controlled release of growth factors. An important prerequisite for the clinical usefulness of a wound dressing is good biocompatibility. Therefore, the biocompatibility of cross-linked gelatin hydrogels films was evaluated in vitro by cytotoxicity tests involving suitable target cells, and in vivo by implantation studies in fullthickness wounds made in mouse and pig animal models.
机译:尽管提供干伤口愈合条件的传统伤口敷料(非闭合性)仍占敷料市场的最大份额,但提供潮湿伤口愈合条件的闭合性敷料,水胶体和水凝胶敷料的使用已大大增加。开发新敷料的下一个重要步骤是引入能够将活性物质输送到伤口部位的含药伤口敷料。例如,已知将外源生长因子施加到伤口部位可增强伤口修复。已经证明通过葡聚糖二醛交联的明胶水凝胶可以控制释放生长因子。伤口敷料的临床实用性的重要前提是良好的生物相容性。因此,在体外通过涉及合适靶细胞的细胞毒性试验评估了交联明胶水凝胶膜的生物相容性,并通过在小鼠和猪动物模型中制作的全厚度伤口中的植入研究,在体内进行了评估。

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