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Preparation and characterisation of novel polycaprolactone-chitosan blends

机译:新型聚己内酯-壳聚糖​​共混物的制备与表征

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This research paper reports on the production of a biocompatible and biodegradable material to be used in a polymer stent used for counteracting the occurrence of anastomotic leakage following gastrointestinal surgery. Chitosan was blended with polycaprolactone in a solvent mixture of acetic acid and water. Membranes were formed with a range of 50/50%, 60/40%, 65/35%, 70/30% and 80/20% polycaprolactone/chitosan. The tensile properties of the blends were examined over a time period to access material degradation. In addition the biocompatibilities of the polycaprolactone/chitosan blends were tested for cytotoxic effect using primary tendon fibroblastic cells. This research concluded that the polycaprolactone/chitosan was non-toxic to the fibroblasts cells in-vitro. Analysis of the mechanical properties of the blends showed a range of mechanical strengths and polymer life spans. Overall, blends of 65/35%, 70/30% and 80/20% polycaprolactone/chitosan emerged as possible candidates for the production of a gastrointestinal stent.
机译:该研究报告报道了用于生物支架的生物相容性和可生物降解材料的生产,该聚合物支架用于抵消胃肠道手术后吻合口漏的发生。将壳聚糖与聚己内酯在乙酸和水的溶剂混合物中共混。形成具有50/50%,60/40%,65/35%,70/30%和80/20%聚己内酯/壳聚糖的膜。在一段时间内检查了共混物的拉伸性能,以了解材料的降解情况。另外,使用初级肌腱成纤维细胞测试了聚己内酯/壳聚糖共混物的生物相容性的细胞毒性作用。这项研究得出的结论是,聚己内酯/壳聚糖对成纤维细胞体外无毒。对共混物的机械性能的分析显示出一定范围的机械强度和聚合物寿命。总体而言,出现了65/35%,70/30%和80/20%的聚己内酯/壳聚糖的共混物可能是生产胃肠支架的候选产品。

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