Kim Young Hoon, Jeong Dong Won, Kim Yoon-Cheol, Sohn Dong Hwan, Park Eun-Seok, Lee Hye Suk
College of Pharmacy, Wonkwang University, Iksan 570-749, Korea.
Arch Pharm Res. 2007 Feb;30(2):260-5. doi: 10.1007/BF02977703.
The pharmacokinetics of active components such as baicalein, wogonin and oroxylin A were evaluated after oral administration of a purified extract of Scutellaria baicalensis GEORGI (PF-2405) containing the high contents of baicalein, wogonin and oroxylin A to rats. Following oral administration of PF-2405 at 10, 20 and 40 mg/kg dose (equivalent to 4.5, 9.0 and 18 mg/kg baicalein), a major constituent baicalein and its active metabolite baicalin showed dose-linear pharmacokinetics as evidenced by unaltered dose-normalized AUC, dose-normalized Cmax, Ae(0-30h) and GI(30h) values. Following oral administration of PF-2405 at three doses (equivalent to 0.4, 0.8 and 1.6 mg/kg wogonin), dose-normalized Cmax and dose-normalized AUC were comparable between the 20 and 40 mg/kg PF2405 doses, but plasma concentrations of wogonin at 10 mg/kg of PF-2405 were not measurable as they were below limit of quantitation (LOQ; 18 pmol/mL). Following oral administration of PF-2405 at the three doses (equivalent to 1.5, 3.0 and 6.0 mg/kg oroxylin A), the concentrations of oroxylin A in plasma, urine and gastrointestine samples were below the assay LOQ (18 pmol/mL). Significant differences in AUCs, Ae(0-30h) and GI(30h) values for baicalein and baicalin were observed after oral administration of pure baicalein (18 mg/kg) and PF-2405 (40 mg/kg). The increases in AUCs of baicalein and baicalin after oral administration of PF-2405 may have been due to the significant decrease in GO(30h) values for baicalein.
给大鼠口服含有高含量黄芩苷、汉黄芩素和木犀草素A的黄芩(PF - 2405)纯化提取物后,评估了黄芩苷、汉黄芩素和木犀草素A等活性成分的药代动力学。以10、20和40 mg/kg剂量(相当于4.5、9.0和18 mg/kg黄芩苷)口服PF - 2405后,主要成分黄芩苷及其活性代谢物黄芩苷呈现剂量线性药代动力学,未改变的剂量归一化AUC、剂量归一化Cmax、Ae(0 - 30h)和GI(30h)值证明了这一点。以三个剂量(相当于0.4、0.8和1.6 mg/kg汉黄芩素)口服PF - 2405后,20和40 mg/kg PF2405剂量之间的剂量归一化Cmax和剂量归一化AUC相当,但10 mg/kg PF - 2405时汉黄芩素的血浆浓度低于定量限(LOQ;18 pmol/mL),无法测量。以三个剂量(相当于1.5、3.0和6.0 mg/kg木犀草素A)口服PF - 2405后,血浆、尿液和胃肠道样品中木犀草素A的浓度低于测定LOQ(18 pmol/mL)。口服纯黄芩苷(18 mg/kg)和PF - 2405(40 mg/kg)后,观察到黄芩苷和黄芩苷的AUCs、Ae(0 - 30h)和GI(30h)值存在显著差异。口服PF - 2405后黄芩苷和黄芩苷AUCs的增加可能是由于黄芩苷的GO(30h)值显著降低。