Chu Da-Feng, Fu Xue-Qi, Liu Wan-Hui, Liu Ke, Li You-Xin
School of Pharmacy, Yantai University, No. 32 Qingquan Road, 264005 Yantai, Shandong Province, PR China.
Int J Pharm. 2006 Nov 15;325(1-2):116-23. doi: 10.1016/j.ijpharm.2006.06.032. Epub 2006 Jun 27.
The purpose of this study was to investigate the pharmacokinetics and in vitro/in vivo correlation (IVIVC) of huperzine A loaded poly(lactic-co-glycolic acid) (PLGA) microspheres in dogs. Several huperzine A loaded PLGA microspheres were prepared by an O/W method and three of them (single dose) were injected intramuscularly (i.m.) or subcutaneously (s.c.) to five beagle dogs, respectively. With the increase of the molecular weight of PLGA and the particle size of microspheres, the in vitro and in vivo release periods of huperzine A were prolonged. After s.c. injection, the release of huperzine A from microspheres was faster than that after i.m. injection. The IVIVC models of huperzine A loaded PLGA microspheres were established successfully and after i.m. administration the linear relationship between the in vitro and the in vivo releases was better than that after s.c. administration. It was also found when the particle size of the microspheres was smaller; the values of correlation coefficient were higher.
本研究旨在考察石杉碱甲聚乳酸-乙醇酸共聚物(PLGA)微球在犬体内的药代动力学及体外/体内相关性(IVIVC)。采用水包油法制备了几种载石杉碱甲的PLGA微球,并将其中三种(单剂量)分别肌肉注射(i.m.)或皮下注射(s.c.)给五只比格犬。随着PLGA分子量和微球粒径的增加,石杉碱甲的体外和体内释放期延长。皮下注射后,微球中石杉碱甲的释放比肌肉注射后更快。成功建立了载石杉碱甲PLGA微球的IVIVC模型,肌肉注射给药后体外和体内释放之间的线性关系优于皮下给药后。还发现当微球粒径较小时,相关系数值较高。