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阿昔洛韦白蛋白微球的制备及体外释药
引用本文:杨秀岭,张志清,董立. 阿昔洛韦白蛋白微球的制备及体外释药[J]. 中国药学杂志, 2000, 35(10): 676-678
作者姓名:杨秀岭  张志清  董立
作者单位:河北医科大学第二医院药剂科!河北石家庄市050000(杨秀岭,张志清,李素民,樊德厚),河北医科大学药学院!94级实习生(董立)
摘    要: 目的 优化阿昔洛韦白蛋白微球的制备工艺,并对其形态学性质、载药量、体外释药进行考察。方法 用乳化热固化法制备微球,用动态透析法进行体外释药。结果 微球平均粒径为(0.94±0.15)μm,载药量为(16.07±1.04)%,体外释药方程1-Q=0.815 e-0.66402t+0.1625e-0.01657tt1/2α=1.044 h,t1/2β=41.82 h。结论 微球外观圆整、均匀,体外释药符合长效制剂的特征。

关 键 词:阿昔洛韦  白蛋白  微球
收稿时间:1998-09-18;
修稿时间:1998-09-18

Studies on the preparation and in vitro release of aciclovir-loaded albumin microspheres
YANG Xiu ling,ZHANG Zhi qing,Dong Li,LI Su min,FAN De hou. Studies on the preparation and in vitro release of aciclovir-loaded albumin microspheres[J]. Chinese Pharmaceutical Journal, 2000, 35(10): 676-678
Authors:YANG Xiu ling  ZHANG Zhi qing  Dong Li  LI Su min  FAN De hou
Affiliation:Department of Pharmacy,The Second Affiliated Hospital of Hebei Medical University,Shijiazhuang 050000,China
Abstract:OBJECTIVE To study the preparation of aciclovir-loaded albumin microspheres (ACV-BSA-MS) and evaluate its morphology,drug loading and release in vitro. METHODS The ACV-BSA-MS was prepared by emulsion-heat stabilization techniques. RESULTS The mean diameter of ACV-BSA-MS prepared under optimum conditions was (0.94±0.15) μm.The drug loading was (16.07±1.04)%.The in vitro release equation was 1-Q=0.8151e-0.66402t+0.1625e-0.01657t,t1/2α=1.044 h,t1/2β=41.82 h. CONCLUSION The ACV-BSA-MS prepared under optimum conditions had regular morphology with a high drug loading and in vitro release properties confirmed to that of long-acting preparations.
Keywords:aciclovir  albumin  microspheres
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