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出 处:《药物分析杂志》2007年第9期1459-1461,共3页Chinese Journal of Pharmaceutical Analysis
摘 要:目的:建立兰索拉唑脂质体包封率的测定方法。方法:利用透析法分离脂质体和游离药物,采用紫外分光光度法测定兰索拉唑脂质体的包封率,在284 nm 处测定兰索拉唑脂质体中的含药量。结果:透析平衡时间为10 h,兰索拉唑浓度在2.1~10.5μg·mL^(-1)范围内线性关系良好(r=0.9998);该方法的平均游离药物回收率(98.5%~99.9%)符合要求;高、中、低3种浓度的日内和日间精密度试验的 RSD 均小于1%;透析24 h 内无渗漏,重现性好。结论:本法便捷、准确,适用于脂溶性药物兰索拉唑脂质体包封率的测定。Objective:To establish a method for determination of the entrapment efficiency of lansoprazole liposomes. Methods:The entrapment efficiency of lansoprazole liposomes was determined by dialysis method with UV for analyzing the amount of lansoprazole. Results :The equilibrium time was 10 h. The calibration curve was linear( r =0. 9998) with in the range of 2. 1 -10. 5 μg · mL^-1 for lansoprazole. The recoveries of the method were 98.5% -99.9%, and the RSDs of the intra -day and inter -day were less than 1%. The leaking percentage in 24 h was neglectable in the process of the dialysis. Conclusion: Dialysis method is convenient and accurate. It is suitable for determining the entrapment efficiency of liposomes of hydrophobic drugs such as lansoprazole.
分 类 号:R917[医药卫生—药物分析学]
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