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一种灵敏快速的超高效液相色谱-串联质谱法的建立与验证,用于同时测定大鼠口服桂枝甘草汤后血浆中七种生物活性化合物。

Development and validation of a sensitive and fast UPLC-MS/MS method for simultaneous determination of seven bioactive compounds in rat plasma after oral administration of Guizhi-gancao decoction.

作者信息

Ji Bin, Zhuo Limeng, Yang Bin, Wang Yang, Li Lin, Yu Miao, Zhao Yunli, Yu Zhiguo

机构信息

Department of Pharmaceutical Analysis, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, China.

Department of Pharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, China.

出版信息

J Pharm Biomed Anal. 2017 Apr 15;137:23-32. doi: 10.1016/j.jpba.2017.01.021. Epub 2017 Jan 9.

Abstract

Rapid, sensitive, selective and accurate UPLC-MS/MS method was developed and fully validated for simultaneous determination of cinnamaldehyde, cinnamic acid, 2-methoxy cinnamic acid, glycyrrhizic acid, glycyrrhetinic acid, liquiritigenin and isoliquiritin in rat plasma after oral administration of Guizhi-gancao decoction. Plasma samples were processed with a simple protein precipitation technique using acetonitrile, followed by chromatographic separation using a Thermo Hypersil GOLD C column. A 11.0min linear gradient elution was used at a flow rate of 0.2mL/min with a mobile phase of 0.1% acetic acid containing 0.2mM ammonium acetate in water and acetonitrile. The analytes and internal standard, schisandrin, were detected using both positive and negative ion electrospray ionization in multiple reaction monitoring mode. The developed method was validated for intra-day and inter-day accuracy and precision whose values fell in the acceptable limits. Matrix effect was found to be minimal. Recovery efficiency of all the analytes was found to be >60%. Stability results showed that the analytes were stable at all the conditions. This validated method was successfully used to study the pharmacokinetics of multiple compounds in rat plasma after oral administration of Guizhi-gancao decoction.

摘要

建立了一种快速、灵敏、选择性强且准确的超高效液相色谱-串联质谱法(UPLC-MS/MS),并对其进行了全面验证,用于同时测定大鼠口服桂枝甘草汤后血浆中肉桂醛、肉桂酸、2-甲氧基肉桂酸、甘草酸、甘草次酸、甘草素和异甘草素的含量。血浆样品采用乙腈简单蛋白沉淀技术处理,然后使用Thermo Hypersil GOLD C柱进行色谱分离。以0.2mL/min的流速进行11.0分钟的线性梯度洗脱,流动相为含0.2mM醋酸铵的0.1%醋酸水溶液和乙腈。采用正离子和负离子电喷雾电离在多反应监测模式下检测分析物和内标五味子醇甲。所建立的方法在日内和日间的准确度和精密度均得到验证,其值均在可接受范围内。发现基质效应最小。所有分析物的回收率均>60%。稳定性结果表明,分析物在所有条件下均稳定。该验证方法成功用于研究大鼠口服桂枝甘草汤后血浆中多种化合物的药代动力学。

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