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首页> 外文期刊>Japanese Journal of Pharmacology >Pharmacokinetics of paeoniflorin after oral administration of Shao-yao Gan-chao Tang in mice.
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Pharmacokinetics of paeoniflorin after oral administration of Shao-yao Gan-chao Tang in mice.

机译:少药干煎汤对小鼠口服of药苷的药代动力学。

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摘要

Paeoniflorin, a monoterpene glycoside, is the principal bioactive component of Paeoniae Radix. The traditional prescription Shao-yao Gan-chao Tang (SGT; Kampo: Shakuyaku-Kanzo-To), which is composed of Paeoniae Radix and Glycyrrhizae Radix, has been widely used in China and Japan. Quantification of paeoniflorin in mouse plasma after oral administration of SGT (at a dose containing 10 mg/kg paeoniflorin) was achieved using a simple and rapid high-performance liquid chromatography method. The plasma concentration-time curves were fitted with mean terminal half-lives (t 1/2) of 116.17 min. The maximum plasma concentration (Cmax) of paeoniflorin was 111.56 ng/ml, time to reach maximum concentration (tmax) was 17.00 min, the area under the plasma concentration-time curve (AUC)0-t was 12293.42 ng x min/ml, clearance/bioavailability (CL/F) value was 644.74 ml/min x kg, apparent volume of distribution/ bioavailability (Vd/F) value was 103.05 l/kg, and the mean residence time (MRT) was 169.64 min. These results, together with the previously reported kinetic data of paeoniflorin after oral administration of Paeoniae Radix extract alone, indicated that absorption of paeoniflorin after oral administration of SGT was significantly greater than that after oral administration of Paeoniae Radix alone.
机译:ter药苷,一种单萜糖苷,是Pa药的主要生物活性成分。由Pa药根和甘草基组成的传统药方少药甘超汤(SGT;甘草:Sha药甘草多)已在中国和日本广泛使用。口服SGT(剂量为10 mg / kg的flor药苷)后,使用简单,快速的高效液相色谱法即可对小鼠血浆中的pa药苷进行定量。血浆浓度-时间曲线拟合的平均终末半衰期(t 1/2)为116.17分钟。 eon药苷的最大血浆浓度(Cmax)为111.56 ng / ml,达到最大浓度的时间(tmax)为17.00 min,血浆浓度-时间曲线(AUC)0-t下的面积为12293.42 ng x min / ml,清除/生物利用度(CL / F)值为644.74 ml / min x kg,表观分布/生物利用度(Vd / F)值为103.05 l / kg,平均停留时间(MRT)为169.64分钟。这些结果,与先前报道的单独口服Pa药提取物后pa药苷的动力学数据一起,表明口服SGT后pa药苷的吸收显着大于单独口服Pa药后的absorption药吸收。

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