Takizawa Yukiho, Morota Takashi, Takeda Shuichi, Aburada Masaki
Department of Drug Metabolism & Disposition, Tsumura Research Institute, Tsumura & Co., Ami-machi, Inashiki-gun, Ibaraki, Japan.
Biol Pharm Bull. 2003 May;26(5):608-12. doi: 10.1248/bpb.26.608.
(-)-Epicatechin-3-O-gallate (ECG), a component of Rhei Rhizoma, is one of the active components of Onpi-to, a herbal medicine composed of five crude drugs (Rhei Rhizome, Glycyrrhizae Radix, Ginseng Radix, Zingiberis Rhizoma and Aconiti Tuber), which has been used in patients with chronic renal failure. Pharmacokinetics of ECG was investigated in male rats employing an HPLC-electrochemical detection method. 1. Following oral administration of ECG, ECG plasma levels revealed curves characterized by peaks at 0.065, 0.063 and 0.085 h corresponding to dosages of 12.5, 25.0 and 50.0 mg/kg at mean concentrations of 49.62, 212.89 and 464.04 ng/ml, respectively. Plasma levels subsequently declined bi-exponentially. ECG demonstrated nonlinear pharmacokinetics in terms of C(max) and AUC(0-inf). 2. The absolute bioavailability values (F) were 1.02, 1.47 and 3.30% at doses of 12.5, 25.0, and 50.0 mg/kg, respectively. 3. Following intravenous injection of ECG, plasma levels of ECG decreased with the gamma-elimination half-life (t(1/2gamma)) of 4.03 h. 4. Following oral administration of ECG, urinary levels of ECG were lower than the quantitation limit. Moreover, cumulative excretion of the metabolites, delta-(3,4-dihydroxyphenyl)-gamma-valerolactone and delta-(3-methoxy-4-hydroxyphenyl)-gamma-valerolactone, was 2.45 and 0.23% of dose, respectively, up to 30 h after dosing.
(-)-表儿茶素-3-O-没食子酸酯(ECG)是大黄的一种成分,是由五种生药(大黄、甘草、人参、干姜和附子)组成的草药温脾汤的活性成分之一,该草药已用于慢性肾衰竭患者。采用高效液相色谱-电化学检测法研究了雄性大鼠体内ECG的药代动力学。1.口服ECG后,ECG血浆水平呈现出曲线,在0.065、0.063和0.085小时出现峰值,分别对应12.5、25.0和50.0mg/kg的剂量,平均浓度分别为49.62、212.89和464.04ng/ml。随后血浆水平呈双指数下降。就C(max)和AUC(0-inf)而言,ECG表现出非线性药代动力学。2.在12.5、25.0和50.0mg/kg剂量下,绝对生物利用度值(F)分别为1.02%、1.47%和3.30%。3.静脉注射ECG后,ECG血浆水平以4.03小时的γ消除半衰期(t(1/2γ))下降。4.口服ECG后,ECG的尿液水平低于定量限。此外,给药后30小时内,代谢物δ-(3,4-二羟基苯基)-γ-戊内酯和δ-(3-甲氧基-4-羟基苯基)-γ-戊内酯的累积排泄量分别为剂量的2.45%和0.23%。