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珊瑚/聚(DL-乳酸)生物可吸收材料的水解降解

Hydrolytic degradation of the coral/poly(DL-lactic acid) bioresorbable material.

作者信息

Li S, Vert M

机构信息

Centre de Recherche sur les Biopolymères Artificiels, Faculté de Pharmacie, Montpellier, France.

出版信息

J Biomater Sci Polym Ed. 1996;7(9):817-27. doi: 10.1163/156856296x00156.

Abstract

A bioresorbable composite material composed of a high molecular weight poly(DL-lactic acid) and granules of natural coral (40/60 w/w) was made by blending in acetone with further evaporation of the solvent. The blend and the unfilled polymer matrix were compression moulded and machined to yield 12 x 12 mm plates of different thicknesses (1.4 mm for the blend vs 2.1 mm for the polymer). The resulting plates were allowed to age at 37 degrees C in a pH 7.4 isoosmolar phosphate buffer solution taken as a model of body fluids. Hydrolytic degradation of the blend was investigated comparatively with the unfilled polymer matrix. The fate of the specimens was monitored by weighing, enzymatic assay, size-exclusion chromatolography and differential scanning calorimetry. Data on water absorption, weight loss, release of L-lactic acid, molecular weight and morphology changes conclusively showed that the presence of coral dramatically modified the degradation characteristics of poly(DL-lactic acid). In particular, the faster internal degradation observed for the unfilled polymer matrix was not detected for the blend. This finding was assigned to the buffering effect of calcium carbonate which neutralized the carboxyl end groups of the degradation products and to the presence of coral/polymer interfaces which facilitated ion exchanges with the external solution, both contributing to eliminate autocatalysis.

摘要

一种由高分子量聚(DL-乳酸)和天然珊瑚颗粒(40/60重量比)组成的生物可吸收复合材料,通过在丙酮中混合并进一步蒸发溶剂制成。将混合物和未填充的聚合物基体进行压缩模塑和加工,制成不同厚度的12×12毫米板材(混合物板材厚度为1.4毫米,聚合物板材厚度为2.1毫米)。将所得板材置于37℃的pH 7.4等渗磷酸盐缓冲溶液中老化,该溶液作为体液模型。将混合物的水解降解与未填充的聚合物基体进行了比较研究。通过称重、酶促分析、尺寸排阻色谱法和差示扫描量热法监测样品的变化情况。关于吸水率、重量损失、L-乳酸释放、分子量和形态变化的数据确凿地表明,珊瑚的存在显著改变了聚(DL-乳酸)的降解特性。特别是,未填充的聚合物基体观察到的较快的内部降解在混合物中未被检测到。这一发现归因于碳酸钙的缓冲作用,它中和了降解产物的羧基端基,以及珊瑚/聚合物界面的存在,其促进了与外部溶液的离子交换,两者都有助于消除自催化作用

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