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作 者:姜英[1] 王晓敏[1] 王艳红[1] 程岚[1] 李学涛[1]
出 处:《中国药房》2015年第31期4399-4401,共3页China Pharmacy
基 金:国家自然科学基金资助项目(No.81102822;81541081);辽宁省科学技术计划项目(No.2014020046)
摘 要:目的:制备转铁蛋白(TF)修饰粉防己碱(TET)与硫酸长春新碱(VCR)的主动靶向脂质体,优化其处方。方法:以硫酸铵梯度法制备TF修饰TET与VCR脂质体,以TET包封率、VCR包封率的综合评分为指标,用星点设计-效应面法优化卵磷脂/胆固醇(EPC/Chol)摩尔比、卵磷脂/聚乙二醇2000-二硬脂酰磷脂酰乙醇胺(EPC/PEG2000-DSPE)摩尔比、TF质量分数,并进行验证试验。结果:最优处方为EPC/Chol摩尔比1.5∶1,EPC/PEG2000-DSPE摩尔比20∶1,TF质量分数0.10%;所得脂质体TET包封率为97.80%,VCR包封率为93.00%,综合评分为94.44(n=3),与其预测值93.81接近。结论:优化所得处方稳定,可用于制备TF修饰TET与VCR脂质体。OBJECTIVE:To prepare transferrin(TF)modified tetrandrine(TET)and vincristine(VCR)active targeting liposomes,and to optimize its formulation. METHODS:TF modified TET and VCR liposomes were prepared by ammonium sulfate gradient method. Using comprehensive score of encapsulation efficiency of TET and VCR as index,central composite design-response surface method was used to optimize and validate mole ratio of EPC/Chol,mole ratio of EPC/PEG2000-DSPE and TF mass fraction. RESULTS:The optimal formulation was that the mole ratios of EPC/Chol and EPC/PEG2000-DSPE were 1.5 ∶ 1 and 20 ∶ 1,TF mass fraction was 0.10%. The encapsulation efficiency of TET and VCR were 97.80% and 93.00%,respectively. The comprehensive score was 94.44(n=3)which was close to the predicted value of 93.81. CONCLUSIONS:The optimal formulation is stable and can be used for the preparation of TF modified TET and VCR liposomes.
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