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机构地区:[1]浙江万里学院生物与环境学院,浙江宁波315100 [2]绍兴文理学院药学系,浙江绍兴312000
出 处:《中国现代应用药学》2011年第6期527-530,共4页Chinese Journal of Modern Applied Pharmacy
基 金:绍兴市科技局重点资助项目(2008A23017)
摘 要:目的建立酮康唑醇质体包封率的微柱凝胶离心-HPLC测定方法。方法药物含量采用HPLC测定,醇质体与游离药物的分离采用葡聚糖凝胶微柱离心法。色谱条件为:色谱柱Sinochrom ODS-BP(4.6 mm×200 mm,5μm),流动相乙腈-水-三乙胺(60∶40∶0.5,磷酸调pH 8.6),流速1.0 mL.min-1,检测波长243 nm,进样量20μL。分离条件为:以2 000 r.min-1离心3 min制备葡聚糖凝胶微柱,测样量0.2 mL,以2 400 r.min-1离心5 min,再用0.2 mL蒸馏水洗脱,重复3次。结果微柱对酮康唑的平均吸附率>99.30%,对空白醇质体洗脱率>99.49%。结论葡聚糖凝胶微柱离心-HPLC可作为醇质体包封率测定的简单快捷方法。OBJECTIVE To develop a determination method for the entrapment efficiency of ketoconazole ethosomes.METHODS The content of ketoconazole was determined by HPLC.The minicolumn of filling dextran gel was adopted to separate the free ketoconazole from ethosome dispersions by centrifugation.Chromatographic conditions were as follows: column was Sinochrom ODS-BP(4.6 mm×200 mm,5 μm) and the mobile phase was acetonitrile-water-triethylamine(60∶40∶0.5,adjust to pH 8.6 using phosphate) with the flow rate of 1.0 mL.min-1,and detection wavelength was 243 nm.The Dextran G-50 minicolumn was spinned at 2 000 r.min-1 for 3 min for removing excess amount of water.The 0.2 mL sample added on prepared column was centrifuged at 2 400 r.min-1 for 5 min,and then washed for 3 times by 0.2 mL of distilled water.RESULTS By flowing through the Dextran G50 minicolumn,the free ketoconazole was adsorbed more than 99.30%,while the average recovery of blank ethosomes was more than 99.49%.CONCLUSION This method is technically simple and rapid to determine entrapment efficiency of ketoconazole ethosomes.
关 键 词:酮康唑醇质体 包封率 微柱凝胶离心法 高效液相色谱法
分 类 号:R917.101[医药卫生—药物分析学]
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