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机构地区:[1]辽宁中医药大学药学院,辽宁大连116600 [2]临沂市食品药品检验检测中心,山东临沂276001
出 处:《中国药房》2016年第22期3034-3036,共3页China Pharmacy
基 金:国家自然科学基金资助项目(No.81541081);辽宁省科学技术计划项目(No.2014020046);辽宁省教育厅重点实验室基础研究项目(No.LZ2015053)
摘 要:目的:建立转铁蛋白修饰长春新碱-粉防己碱脂质体中主药含量及脂质体包封率的测定方法。方法:采用高效液相色谱法测定长春新碱含量,色谱柱为依利特C_(18),流动相为甲醇-15%三乙胺水溶液(70∶30),流速为1.0 ml/min,检测波长为297 nm,柱温为30℃,进样量为20μl;采用葡聚糖凝胶柱色谱法分离脂质体与游离药物,计算包封率。结果:长春新碱检测质量浓度为160-1 600μg/ml(r=0.999 8,n=5),平均加样回收率为99.20%(RSD=0.26%,n=9),精密度RSD为0.070%(n=5)。脂质体中长春新碱的平均含量为0.790 mg/ml(RSD=0.15%,n=3),平均包封率为85.94%(RSD=2.08%,n=3)。结论:该方法准确可靠、简单快速,可用于转铁蛋白修饰长春新碱-粉防己碱脂质体中长春新碱的含量及包封率测定。OBJECTIVE:To establish the method for the determination of main components content and entrapment efficiency of transferrin modified vincristine-tetrandrine liposomes. METHODS:HPLC method was adopted to determine the content of vincristine. The determination was performed on ELITE C_(18) column with mobile phase consisted of methanol-15% triethylamine(70 ∶30)at a flow rate of 1.0 ml/min. The determination wavelength was set at 297 nm and column temperature was 30 ℃. The sample size was 20 μl. Free drug was isolated from liposomes by dextran gel column chromatography,and entrapment efficiency was determined. RESULTS:The linear range of vincristine was 160-1 600 μ g/ml(r=0.999 8,n=5) with average recovery of 99.20%(RSD=0.26%,n=9). RSD of precision test was 0.070%(n=5). The average content of vincristine in liposomes was 0.790mg/ml(RSD=0.15%,n=3),and the average entrapment efficiency was 85.94%(RSD=2.08%,n=3). CONCLUSIONS:The method is accurate,reliable,simple and rapid,and can be used for the determination of the content and entrapment efficiency of vincristine in transferrin modified vincristine-tetrandrine liposomes.
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