Bittner B, Ronneberger B, Zange R, Volland C, Anderson J M, Kissel T
Department of Pharmaceutics and Biopharmacy, Philipps-University, Marburg, Germany.
J Microencapsul. 1998 Jul-Aug;15(4):495-514. doi: 10.3109/02652049809006876.
To study the influence of polymer purity on microsphere characteristics, bovine serum albumin (BSA) loaded biodegradable microspheres were prepared by spray drying using two samples of poly(lactide-co-glycolide), PLG, (50:50, mwt = 35 and 69 kDa). Polymer properties were varied by DL-lactide and glycolide addition or by ultrafiltration. While the effective drug loading was not affected by polymer purity, Tg was decreased with increasing monomer and oligomer content. The removal of these low molecular weight substances by ultrafiltration led to a narrower molecular weight distribution compared to the untreated PLG. Concerning the polymer with the higher molecular weight, microsphere morphology was also strongly affected by polymer composition. In contrast to the non-modified PLG, monomer addition yielded particles with a much smoother surface structure. Moreover, in vitro cytotoxicity of the microspheres prepared from the polymer pretreated by ultrafiltration was significantly reduced, whereas monomer addition caused a dramatic decrease of cells surviving contact with the microsphere extract. The in vivo degradation rate of the ultrafiltered microspheres was decreased and as a result, protein release at later times was slowed down. Furthermore, depending on the effective drug loading level, monomer addition resulted in a decrease in the initial protein burst. It can be concluded that the effect of low molecular weight impurities in a polymer on microsphere characteristics and on cytotoxicity cannot be ignored. Their elimination is possible by ultrafiltration.
为研究聚合物纯度对微球特性的影响,使用聚丙交酯-乙交酯(PLG,50:50,分子量分别为35 kDa和69 kDa)的两个样品,通过喷雾干燥法制备了负载牛血清白蛋白(BSA)的可生物降解微球。通过添加DL-丙交酯和乙交酯或超滤来改变聚合物的性质。虽然有效载药量不受聚合物纯度的影响,但玻璃化转变温度(Tg)会随着单体和低聚物含量的增加而降低。与未处理的PLG相比,通过超滤去除这些低分子量物质会导致分子量分布变窄。对于分子量较高的聚合物,微球形态也受到聚合物组成的强烈影响。与未改性的PLG相比,添加单体得到的颗粒表面结构更光滑。此外,由超滤预处理的聚合物制备的微球的体外细胞毒性显著降低,而添加单体则导致与微球提取物接触的存活细胞数量急剧减少。超滤微球的体内降解速率降低,结果后期蛋白质释放减缓。此外,根据有效载药量水平,添加单体导致初始蛋白质突释减少。可以得出结论,聚合物中低分子量杂质对微球特性和细胞毒性的影响不可忽视。通过超滤可以去除这些杂质。