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作 者:张家伟[1,2] 王晓明[1] 潘桂湘[1] 李婷婷[1,2] 朱彦[1,2]
机构地区:[1]天津中医药大学天津市现代中药重点实验室-省部共建国家重点实验室(培育),天津300193 [2]天津国际生物医药联合研究院,天津300457
出 处:《辽宁中医杂志》2016年第8期1717-1720,共4页Liaoning Journal of Traditional Chinese Medicine
基 金:国家自然科学基金资助项目(81173525;813031827);国际科技合作专项(2013DFA31620)
摘 要:目的:采用UPLC-MS/MS法测定大鼠灌服稳心颗粒后血浆中3个皂苷成分的浓度,并研究其药动学特征。方法:血浆样品以甲醇-乙腈(1:1)沉淀蛋白,采用CORTECS-C18色谱柱(2.1 mm×50 mm,1.6μm),以0.1%甲酸水(A)-乙腈(含0.1%甲酸)(B)为流动相进行梯度洗脱,于ESI负离子模式下检测。结果:人参皂苷Rd和Rg1在0.5~20 ng/m L,人参皂苷Rb1在1~40 ng/m L范围内线性关系良好(r大于0.99),3个成分的提取回收率为人参皂苷Rd105.2%~120.7%,人参皂苷Rg1 101.9%~123.9%,人参皂苷Rb1 92.8%~116.9%。结论:该方法简便、准确、灵敏,可用于稳心颗粒药动学研究。Objective: To determine three saponins in rats plasma by UPLC- MS/MS method and study their pharmacokinetics. Methods: Sample preparation was performed by a protein precipition with methanol and acetonitrile( 1: 1). The analysis was in the flow rate of 0. 5 m L/min,the column temperature of 40℃ and the injection volume of 5 μL by gradient elution on a CORTECS- C18column( 2. 1 mm × 50 mm,1. 6 μm) and the mobile phase was 0. 1% formic acid in water( A)- 0. 1% formic acid of acetonitrile( B). Results: All calibration curves had good linearity( r 〉 0. 99) over the concentration ranges of 0. 5- 20 ng·m L-1for ginsenoside Rd and ginsenoside Rg1 1- 40 ng·m L-1for ginsenoside Rb1. The method recoveries of three saponins were 105.2%- 120. 7% for ginsenoside Rd,101. 9%- 123. 9% for ginsenoside Rg1,92. 8%- 116. 9% for ginsenoside Rb1. Conclusion:The above mentioned method is simple,accurate and sensitive for determination of saponins in rats plasma. and has been successfully applied to the study of pharmacokineties of wenxin Granules.
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