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作 者:陈超[1] 邓英杰[1] 王晓宇[1] 董晓东[1]
出 处:《中国医药导报》2009年第36期68-70,共3页China Medical Herald
基 金:国家"863"计划资助项目(2007AA021810)
摘 要:目的:建立测定盐酸伊立替康脂质体包封率的方法。方法:通过微柱离心分离盐酸伊立替康脂质体和游离药物,以HPLC法测定药物含量,计算包封率。结果:Sephadex G-50微型柱可完全吸附盐酸伊立替康游离药物,空白脂质体回收率为98.2%~100.7%,脂质体和游离药物得到良好的分离;在选定色谱条件下,辅料不干扰测定,盐酸伊立替康质量浓度在1.1~10.6mg/L范围内线性关系良好(r=0.9997),日内和日间精密度(RSD)均<2%,加样回收率为97.6%~100.7%。结论:微柱离心-HPLC法可用于盐酸伊立替康脂质体包封率的测定。Objective:To establish a method for the determination of entrapment efficiency of irinotecan liposomes. Methods:Minicolumn centrifuge method was employed to separate the free drug from the liposomes. The content of irinotecan was quantified by HPLC. Results:Sephadex G-50 filling minicolumn could completely adsorb free irinotecan. The recovery of blank liposomes was in a range of 98.2%-100.7% by minicolumn centrifuge method. Irinotecan liposomes and free irinotecan could be well separated. A calibrated linear curve of irinotecan was within 1.1-10.6 mg/L ( r=0.999 7). Intra-day and inter-day precision (RSD) were both less than 2%. The recovery of irinotecan with blank liposomes was from 97.6% to 100.7%. Conclusion:The minicolumn centrifuge-HPLC method can be used for the determination of entrapment efficiency of irinotecan liposomes.
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