摘要
目的:建立高效液相色谱测定麻疯树提取物中佛波酯含量的方法。方法:直接用二氯甲烷溶液稀释后,过滤、进样,流动相:乙腈/水(梯度洗脱),柱温25℃,流速1.0 ml/min,检测波长280 nm,标准曲线范围15.6~250.0μg/m L,相关系数R=0.9999,检测时间40 min以内提取麻疯树提取液样品。结果:佛波酯标准曲线范围15.6~250.0μg/m L,相关系数R=0.9999,加样平均回收率91.2%-94.6%,精密度RSD 1.3%,检出限5.0μg/m L。结论:该分析方法准确、样品处理方法简单、快速,适合大批量麻疯树提取物中佛波酯含量测定。
Objective: To develop a method for determination of phorbol ester in Jatropha curcas L extracts by HPLC. Meth-ods: Phorbol ester extract samples were diluted with CHCl3, filtered and injected into HPLC. The chromatographic separation was a-chieved on a reverse phase C18 column with gradient elution, using a mobile phase of acetonitrile/ water; detector wave was set at 280nm, column temptation was 25℃ , flow rate was 1. 0 ml/ min, and linear range was 15. 6-250 μg/ ml. Detection time was less than 40min. Results: The cablication curves of phorbol ester showed good linearity with correlation coefficient of 0. 9999. The mean recov-ery of spiked samples were from 91. 2% ~ 94. 6% . The RSD of precision was 1. 3% . The detection limits of phorbol ester was 5. 0μg/ mL. Conclusions: The results show that the method is simple and sensitive, and can be applied to routine analysis of phorbol ester in Jatropha curcas L extracts.
出处
《中国民康医学》
2015年第16期62-64,共3页
Medical Journal of Chinese People’s Health
基金
国家科技支撑计划资助<抗血吸虫感染新植物药研制课题>项目编号(2009BAI78B04)
湖北省卫生厅年度科研项目XN2011-11
湖北省首届医学领军人才培养人才项目