摘要
PL 与 PL EG是生物降解、生物相容的高分子材料 ,利用它们作为药物控释载体已引起人们广泛的重视。我们合成了含不同 PEG链段长度的 PL EG共聚物 ,并利用 PL 与 PL EG这两种材料各自的优点制备载有人绒毛促性腺激素 (h CG)的共混微球以提高 h CG在微球中的包埋率 ,结果表明采用 P(L- co- PEG6 0 0 0 ) (90 :10 )与 PL共混制备得到的微球中 ,h CG的包埋率高于单独用 PL 或 PL EG制得的微球。h CG的体外释放为突破 -缓释过程 。
PL and PLEG are biodegradable, biocompatible polymers. They have been widely used for controlled release of drugs. We synthesized PLEG copolymers containing PEG segments with various molecular weight and prepared hCG loaded PL/PLEG blend microspheres to improve hCG entrapment efficiency. It was shown that the hCG entrapment effciency of PL/PLEG microspheres was higher than that of PL or PLEG microspheres when P(L co PEG6000)(90∶10) was used. In vitro release test showed that the release of hCG was a burst slow process, which was thought to be good for antigens to produce antibodies.
出处
《生物医学工程学杂志》
EI
CAS
CSCD
北大核心
2000年第1期5-9,共5页
Journal of Biomedical Engineering
关键词
共混微球
药物控释载体
聚丙交酯
PLEG
Polylactide Poly(lactide-co-polyethylene glycol) Blend Microspheres Entrapment efficiency of protein