GU Pan, LIU Rui-Juan, CHENG Min-Lu, WU Yao, ZHENG Lu, LIU Yu-Jie, MA Peng-Cheng, DING Li. Simultaneous quantification of chlorogenic acid and taurocholic acid in human plasma by LC-MS/MS and its application to a pharmacokinetic study after oral administration of Shuanghua Baihe tablets[J]. Chinese Journal of Natural Medicines, 2016, 14(4): 313-320.
Citation: GU Pan, LIU Rui-Juan, CHENG Min-Lu, WU Yao, ZHENG Lu, LIU Yu-Jie, MA Peng-Cheng, DING Li. Simultaneous quantification of chlorogenic acid and taurocholic acid in human plasma by LC-MS/MS and its application to a pharmacokinetic study after oral administration of Shuanghua Baihe tablets[J]. Chinese Journal of Natural Medicines, 2016, 14(4): 313-320.

Simultaneous quantification of chlorogenic acid and taurocholic acid in human plasma by LC-MS/MS and its application to a pharmacokinetic study after oral administration of Shuanghua Baihe tablets

  • An LC-MS/MS method was developed and validated for the simultaneous quantification of chlorogenic acid (CGA) and taurocholic acid (TCA) in human plasma using hydrochlorothiazide as the internal standard. The chromatographic separation was achieved on a Hedera ODS-2 column with a gradient elution using 10 mmolL-1 of ammonium acetate buffer solution containing 0.5% of formic acid -acetonitrile as mobile phase at a flow rate of 300 Lmin-1. The detection was performed on a triple quadrupole tandem mass spectrometer by multiple reaction monitoring in negative ESI mode. The method was fully validated over the concentration ranges of 0.1-10 ngmL-1 for CGA and 2-150 ngmL-1 for TCA. It was successfully applied to a pharmacokinetic study of CGA and TCA in healthy Chinese volunteers after oral administration of Shuanghua Baihe tablets (SBTs). In the single-dose study, the maximum plasma concentration (Cmax), time to reach Cmax (Tmax) and elimination half-life (t1/2) of CGA were (0.763 80.542 0) ngmL-1, (1.00.5) h, and (1.30.6) h, respectively. In the multiple-dose study, the Cmax, Tmax and t1/2 of CGA were (0.663 70.583 3) ngmL-1, (1.10.5) h, and (1.40.7) h, respectively. For TCA, no significant characteristic increasing plasma TCA concentration-time curve was found in the volunteers after oral administration of SBTs, indicating its complicated process in vivo as an endogenous ingredient.
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