Simultaneous in vivo RP‐HPLC‐DAD quantification of multiple‐component and drug–drug interaction by pharmacokinetics, using 6,7‐dimethylesculetin, geniposide and rhein as examples

Abstract

ABSTRACTIncreasing evidence has demonstrated that multidrug combinations could amplify the therapeutic efficacies of each agent. Interestingly, the pharmacological effect of traditional Chinese medicine (TCM) is usually attributed to the drug‐interaction property (synergism) of multiple active constituents. Pharmacokinetics is a useful means of evaluating the drug interactions of major active compounds in TCM. A simple, sensitive and reliable RP‐HPLC‐DAD method has been developed to simultaneously quantify 6,7‐dimethylesculetin (D), geniposide (G) and rhein (R), which are the active ingredients in Yin–Chen–Hao–Tang (YCHT), performing drug‐interaction pharmacokinetics studies in vivo. Plasma samples were prepared using methanolic precipitation, a filtration step, and then injection of the methanolic extract onto a Nova‐Pak C18 Guard‐Pak™ guard column with a gradient mobile phase. Triple‐wavelength diode array detection was set at λmax values of 343 nm for D, 241 nm for the G, and 259 nm for R. Our results successfully demonstrate that this method has excellent and satisfactory selectivity, sensitivity, linearity, precision, accuracy and recovery. In healthy rats, the estimated pharmacokinetic parameters (i.e. Cmax, AUC and Cl) of D, G and R, when administered with COC (a combination of D, G and R), were Cmax 16.05 mg/L, AUC 108.96 mg h/L and Cl 0.36 L/h for D; Cmax 9.35 mg/L, AUC 64.71 mg h/L and Cl 0.88 L/h for G; and Cmax 14.18 mg/L, AUC 57.98 mg h/L and Cl 1.77 L/h for R. Here, we report that the COC combination could significantly increase the plasma level and slow the elimination rate compared with any one or two of the three individual compounds, which may indicate a drug–drug interaction. Copyright © 2011 John Wiley & Sons, Ltd.