摘要
目的探索用聚乳酸-羟基乙酸共聚物(PLGA)微球静脉给药实现抗结核药丙硫异烟胺肺部靶向输送的可行性。方法利用单因素分析方法,筛选出丙硫异烟胺-乳酸-羟基乙酸共聚物微球制备的最佳工艺条件;利用桨法研究了载药微球体外释药的规律;利用BALB/C小鼠研究了丙硫异烟胺乳酸-羟基乙酸共聚物微球静脉给药后的体内组织分布。结果制得的微球形态圆整,微球平均粒径为(9.86±1.38)μm,粒径在7～15μm的占81.53%;丙硫异烟胺的包封率为(32.70±0.37)%,载药量为(8.48±0.24)%;丙硫异烟胺乳酸-羟基乙酸共聚物微球体外释药符合Higuchi方程(Q=4.430 3t1/2+7.724 1),释药较慢;体内分布试验表明,微球混悬剂静脉给药后丙硫异烟胺在肺中的浓度显著高于普通注射剂,而且保持较长时间。结论微球制备工艺稳定,具有可重复性,微球在体外以及小鼠体内的释放结果和组织分布表明,微球有明显的缓释作用和肺靶向性。
OBJECTIVE To testify the feasibility of targeted delivery of protionamide to lung through the iv administration of the biodegradable poly（ laetic-co-glycollic acid） （PLGA）microspheres. METHODS Based on the single-factor study, the preparation of protionamide-PLGA mierospheres was optimized. The surface morphology of the microspheres was observed by scanning electron micro- scope （SEM）. The mean diameter and the size distribution of microsphere, the drug loading, the incorporation efficiency, drug release in vitro, stability and tissue distribution after intravenous administration were also evaluated, respectively. RESULTS Protionamide- PLGA mierospheres were regular and spherical in shape. The average particle size was （9.86± 1.38 ） μm and over 81.53 % of the mi- crospheres was in the range of 7 - 15 μm. The drug loading and encapsulated ratio was （32. 70±0. 37）% and （8.48±0. 24）% , re- spectively. The in vitro drug release could be well fitted by the Hignchi equation （ Q =4. 430 3t1/2 ＋7.724 1, r =0. 991 3）. Compared with the aqueous formulation, the drug level in lung of BALB/C mice in microsphere group was much higher, and also kept for longer time. CONCLUSION The protionamide-PLGA microspheres prepared in this study show significant sustained release and lung targeting effect.
出处
《中国药学杂志》
CAS
CSCD
北大核心
2012年第22期1834-1838,共5页
Chinese Pharmaceutical Journal
