Sun Rongjin, Zeng Min, Du Ting, Li Li, Yang Guangyi, Hu Ming, Gao Song
College of Pharmacy, Hubei University of Medicine, 30 South Renmin Road, Shiyan, Hubei, China; Department of Pharmacological and Pharmaceutical Sciences, College of Pharmacy, The University of Houston, 1441 Moursund Street, Houston, TX 77030, USA.
Department of Pharmacy, Taihe Hospital, Hubei University of Medicine, 32 South Renmin Road, Shiyan, Hubei, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Oct 15;1003:12-21. doi: 10.1016/j.jchromb.2015.09.004. Epub 2015 Sep 11.
The purpose of this study is to develop and validate an UPLC-MS/MS method to quantify different marker compounds from Xiao-Chai-Hu-Tang (XCHT, a Chinese traditional herbal) in biological samples and apply the method to pharmacokinetic study. A Waters BEH C18 UPLC column was used with acetonitrile/0.1% formic acid mobile phases. The mass analysis was performed in a triple quadrupole mass spectrometer using multiple reaction monitoring (MRM) with positive scan mode. A one-step protein precipitation by methanol was used to extract the analytes from blood. Seventeen commercially available compounds from the different compositing herbals were selected as markers. The results revealed that all of the calibration curves showed good linear regression (r(2)>0.9918). The intra-day and inter-day precisions (RSD) of all of these markers at three different levels were less than 15.0% and the bias of the accuracies ranged from -13.5% to 16.6%.The extraction recoveries of all of these 17 markers were from 70.8% to 113.7% and the matrix effects ranged from 71.8% to 114.8%. The stabilities of these compounds in blood were evaluated by analyzing three replicates of QC samples at three different concentrations following storage at 25°C for 6h, 4°C for 24h, and -80°C for 30 days. All the samples displayed 85-115% precision and accuracy after various stability tests. The validated method was successfully applied to pharmacokinetic study in A/J mouse with oral administration of XCHT. All of these markers were detected and the pharmacokinetic parameters of 8 compounds were able to be calculated. This method is sensitive and reproducible that can be used for XCHT's in vivo study.
本研究的目的是开发并验证一种超高效液相色谱-串联质谱(UPLC-MS/MS)方法,用于定量生物样品中小柴胡汤(一种中药)中的不同标志物化合物,并将该方法应用于药代动力学研究。使用沃特世BEH C18超高效液相色谱柱,以乙腈/0.1%甲酸为流动相。在三重四极杆质谱仪中采用多反应监测(MRM)正离子扫描模式进行质量分析。采用甲醇一步沉淀蛋白法从血液中提取分析物。从不同组成草药中选择了17种市售化合物作为标志物。结果显示,所有校准曲线均呈现良好的线性回归(r(2)>0.9918)。所有这些标志物在三个不同水平的日内和日间精密度(RSD)均小于15.0%,准确度偏差范围为-13.5%至16.6%。这17种标志物的提取回收率为70.8%至113.7%,基质效应范围为71.8%至114.8%。通过分析在25°C下储存6小时、4°C下储存24小时和-80°C下储存30天的三个不同浓度的质量控制样品的三个重复样本来评估这些化合物在血液中的稳定性。经过各种稳定性测试后,所有样品的精密度和准确度均在85%-115%之间。经过验证的方法成功应用于A/J小鼠口服小柴胡汤的药代动力学研究。所有这些标志物均被检测到,并且能够计算8种化合物的药代动力学参数。该方法灵敏且可重复,可用于小柴胡汤的体内研究。