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Hydrolytic degradation of PLLA/PCL microporous membranes prepared by freeze extraction

机译:冷冻提取法制备的PLLA / PCL微孔膜的水解降解

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摘要

Poly(L-lactic acid) - Poly(ε-caprolactone) blends (PLLA/PCL) porous membranes were prepared by freeze extraction (a modification of freeze drying) with ratios 100/0, 80/20, 60/40, 40/60, 20/80, 0/100 in weight. Degradation of the membranes in phosphate buffer solution (PBS) up to 65 weeks was studied using weight loss measurements, high performance liquid chromatography (HPLC), differential scanning calorimetry (DSC), mechanical indentation, gel permeation chromatography (GPC), and scanning electron microscopy (SEM). Degradation rate as observed by weight loss and reduction of molecular weight and mechanical properties depended on the composition of the blends. In most blends the degradation was more prominent in the PLLA phase and was accompanied by consequent recrystallization that formed a crystalline phase with increased resistance to hydrolysis. Occurrence of such crystalline phases and degradation of intercrystalline domain led to formation of nearly monodisperse molecular weight populations.Membranes with only 20% PCL presented favorable behavior compared to pure PLLA membranes as reflected in a lower degradation rate and a limited loss of the mechanical properties. At the same time, degradation rate of 80/20 membranes was enhanced with respect to pure PCL, and membranes were stiffer than PCL membranes at all degradation times. This composition could thus be useful for use in tissue engineering for bone or cartilage applications.
机译:聚(L-乳酸)-聚(ε-己内酯)共混物(PLLA / PCL)多孔膜通过冷冻萃取(冷冻干燥的改进)以比例100 / 0、80 / 20、60 / 40、40 / 60、20 / 80、0 / 100重量。使用失重测量,高效液相色谱(HPLC),差示扫描量热法(DSC),机械压痕,凝胶渗透色谱(GPC)和扫描电子研究了磷酸盐缓冲液(PBS)中长达65周的膜降解情况显微镜(SEM)。通过重量损失观察到的降解速率以及分子量和机械性能的降低取决于共混物的组成。在大多数混合物中,降解在PLLA相中更为明显,并伴随着随后的重结晶,形成了具有增强的抗水解性的结晶相。这种晶相的出现和晶间结构域的降解导致形成几乎单分散的分子量群。与纯PLLA膜相比,仅含20%PCL的膜表现出良好的性能,这反映出较低的降解率和有限的机械性能损失。同时,相对于纯PCL,80/20膜的降解率提高了,并且在所有降解时间下,膜都比PCL膜坚硬。因此,该组合物可用于组织工程中的骨或软骨应用。

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  • 来源
    《Polymer Degradation and Stability》 |2012年第9期|p.1621-1632|共12页
  • 作者单位

    Centro de Biomateriales e Ingenieria Tisular, Universidad Politecnica de Valencia, Camino de Vera s, Edifido 8E., Planta 1, 46071 Valencia, Spain,Universidad Nacional de Colombia - Sede Bogota, Facultad de Ingenieria, Departamento de Ingenieria Quimica y Ambiental, Grupo de Procesos Quimicos y Bioquimkos - Carrera 30 No. 45-03, Edifido 453, Oficina 301, 111321 Bogota, Colombia;

    Centro de Biomateriales e Ingenieria Tisular, Universidad Politecnica de Valencia, Camino de Vera s, Edifido 8E., Planta 1, 46071 Valencia, Spain,Centro de Investigation Principe Felipe, Av. Autopista del Saler 16, 46073 Valencia, Spain,CIBER de Bioingenieria, Biomateriales y Nanomedicina (CIBER-BBN), Valencia, Spain;

    Universidad Nacional de Colombia - Sede Bogota, Facultad de Ingenieria, Departamento de Ingenieria Quimica y Ambiental, Grupo de Procesos Quimicos y Bioquimkos - Carrera 30 No. 45-03, Edifido 453, Oficina 301, 111321 Bogota, Colombia;

    Centro de Biomateriales e Ingenieria Tisular, Universidad Politecnica de Valencia, Camino de Vera s, Edifido 8E., Planta 1, 46071 Valencia, Spain,Centro de Investigation Principe Felipe, Av. Autopista del Saler 16, 46073 Valencia, Spain,CIBER de Bioingenieria, Biomateriales y Nanomedicina (CIBER-BBN), Valencia, Spain;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    poly(L-lactic acid); poly(e-caprolactone); polyester blends; hydrolytic degradation;

    机译:聚(L-乳酸);聚(ε-己内酯);聚酯共混物;水解降解;

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