摘要
采用乳液固化法制备了肝素钠-牛血清白蛋白毫微粒,并以口服给药的形式,研究毫微粒的肝靶向性。透射电子显微镜测定毫微粒的平均粒径为184±31nm(n=300)。以5-氟尿嘧啶为模型药物,将5-氟尿嘧啶肝素钠-白蛋白毫微粒在酸性条件下100℃水解20h,测得5-氟尿嘧啶的平均包封率为29.5%。体外试验结果表明,5-氟尿嘧啶毫微粒在37℃的稀盐酸液中72h累计释药达79.48%。
Fluorourail nanoparticle was prepared by emusion method, heparin and albuminbeing chosen as carrier. The particle size distribution was measured and the arithmetic mean diam-eter was 184±31 nm(n=300). The encapsulation efficiency of the 5-FU nanoparticle was deter-mined with the result of 29.5%within 72 hours up to 79%drug release was observed from hep-arin-albumin nanoparticles.
出处
《中国药学杂志》
CAS
CSCD
北大核心
1995年第12期728-729,共2页
Chinese Pharmaceutical Journal
基金
国家自然科学基金