摘要
目的:测定静注万乃洛韦聚氰基丙烯酸正丁酯毫微粒(VACVPBCANP)冻干剂和万乃洛韦小鼠体内的分布。方法:用体外肝细胞培养及摄取实验研究VACVPBCANP对肝细胞的胞内靶向性。结果:VACVPBCANP静注后15min即有74.49%的VACV集中在肝脏,比VACV注射液提高了2.99倍,肾脏分布量降低了5.46倍。
OBJECTIVE:To study the distribution of VACV PBCA NP in visceras of mice.METHODS:Uptake of hepotocytes was used to study the permeation of VACV PBCA NP cross the liver cell membrane.HPLC was used to determine the contents of ACV in visceras.RESULTS:The content of VACV PBCA NP in liver was found to be 74.79% of total amount 15 min after iv administration,which was 2.99 times higher than value of VACV injection.While content in kidney was 5.46 times lower than that of VACV in injection.The VACV PBCA NP was found in liver cell of mice by TEM method.CONCLUSIONS:The cell uptake by rat hepotocytes in vitro demonstrated that nanoparticles could greatly increase the amount of VACV uptaking by cell.
出处
《中国医院药学杂志》
CAS
CSCD
北大核心
1999年第1期15-18,共4页
Chinese Journal of Hospital Pharmacy
基金
国家自然科学基金
关键词
万乃洛韦
毫微粒
肝细胞
胞内靶向性
valaciclovir,aciclovir nanoparticles,cell permeation