Cao X, Schoichet M S
Department of Chemical Engineering and Applied Chemistry, University of Toronto, Ontario, Canada.
Biomaterials. 1999 Feb;20(4):329-39. doi: 10.1016/s0142-9612(98)00172-0.
Nerve growth factor (NGF) may enhance axonal regeneration following injury to the central nervous system (CNS), such as after spinal cord injury. The release profile of NGF, co-encapsulated with ovalbumin, was tailored from biodegradable polymeric microspheres using both polymer degradation and protein loading. Biodegradable polymeric microspheres were prepared from PLGA 50/50, PLGA 85/15, PCL and a blend of PCL/PLGA 50/50 (1:1, w/w), where the latter was used to further tailor the degradation rate. The amount of protein loaded in the microspheres was varied, with PCL encapsulating the greatest amount of protein and PLGA 50/50 encapsulating the least. A two-phase release profile was observed for all polymers where the first phase resulted from release of surface proteins and the second phase resulted predominantly from polymer degradation. Polymer degradation influenced the release profile most notably from PLGA 50/50 and PLGA 85/15 microspheres. The amount and bioactivity of released NGF was followed over a 91 d period using a NGF-ELISA and PC12 cells, respectively. NGF was found to be bioactive for 91 d, which is longer than previously reported.
神经生长因子(NGF)可能会促进中枢神经系统(CNS)损伤后的轴突再生,比如脊髓损伤后。与卵清蛋白共包封的NGF的释放曲线,是通过聚合物降解和蛋白质负载,从可生物降解的聚合物微球中定制出来的。可生物降解的聚合物微球由聚乳酸-羟基乙酸共聚物50/50(PLGA 50/50)、聚乳酸-羟基乙酸共聚物85/15(PLGA 85/15)、聚己内酯(PCL)以及PCL/PLGA 50/50(1:1,w/w)的混合物制备而成,其中后者用于进一步调整降解速率。微球中负载的蛋白质量各不相同,PCL包封的蛋白量最多,PLGA 50/50包封的蛋白量最少。所有聚合物均观察到两相释放曲线,其中第一相源于表面蛋白的释放,第二相主要源于聚合物降解。聚合物降解对PLGA 50/50和PLGA 85/15微球的释放曲线影响最为显著。分别使用NGF-ELISA和PC12细胞,在91天的时间内跟踪释放的NGF的量和生物活性。发现NGF在91天内具有生物活性,这比之前报道的时间更长。