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首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Comparative pharmacokinetic study of paeoniflorin after oral administration of decoction of Radix Paeoniae Rubra and Radix Paeoniae Alba in rats.
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Comparative pharmacokinetic study of paeoniflorin after oral administration of decoction of Radix Paeoniae Rubra and Radix Paeoniae Alba in rats.

机译:oral药丹参和赤Alba药汤大鼠口服of药后的药代动力学比较研究。

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An investigation was designed and conducted to compare the pharmacokinetics difference of paeoniflorin after oral administration of the extracts of Radix Paeoniae Rubra and Radix Paeoniae Alba to rats on separate occasions. Quantification of paeoniflorin in rat plasma was achieved using a simple and rapid HPLC method for pharmacokinetic study. After oral administration of decoctions of Radix Paeoniae Rubra and Radix Paeoniae Alba, paeoniflorin was absorbed and reached a maximum concentration of 3.69+/-1.46 and 1.46+/-0.29 (p0.05)microg/ml at 1.67+/-0.43 and 0.80+/-0.35 h (p0.05), respectively. Compared to the AUC (18.85+/-7.54 microg h/ml) after oral administration of the paeoniflorin solution, a smaller AUC (10.61+/-1.51 microg h/ml, p0.05) and a larger AUC (24.89+/-7.41 microg h/ml) of paeoniflorin after oral administration of the decoctions of Radix Paeoniae Alba and Radix Paeoniae Rubra were obtained, respectively. There were statistically significant differences in pharmacokinetic parameters of paeoniflorin including the t(max), C(max), AUC, t(1/2), CL, and V(d) among the animals orally administered the decoctions of Radix Paeoniae Rubra and Radix Paeoniae Alba. In particular, the parameters of t(max), C(max), and AUC of paeoniflorin were remarkably increased (P0.05, P0.001) when oral administering paeoniflorin in the decoctions of Radix Paeoniae Rubra, but t(1/2), V(d), and CL were decreased (P0.05 or P0.01), in comparison of the decoction of Radix Paeoniae Alba.
机译:设计并进行了一项研究,以比较在单独的情况下,将Pa药丹参和Alba药提取物分别口服给予大鼠后,pa药苷的药代动力学差异。使用简单,快速的HPLC方法进行药代动力学研究,即可定量大鼠pa药中的flor药苷。口服Pa药丹参和赤Alba药汤后,pa药苷被吸收,最大浓度为1.69 +/- 0.43和0.80,分别为3.69 +/- 1.46和1.46 +/- 0.29(p <0.05)microg / ml。分别为+/- 0.35小时(p <0.05)。与口服eon药苷溶液后的AUC(18.85 +/- 7.54 microg h / ml)相比,较小的AUC(10.61 +/- 1.51 microg h / ml,p <0.05)和较大的AUC(24.89 +/-)口服Pa药丹参和Ru药丹参汤后分别获得7.41微克/毫升的)药苷。 Pa药和and药煎服的动物中of药苷的药代动力学参数在统计学上有显着差异,包括t(max),C(max),AUC,t(1/2),CL和V(d)。 Pa药丹参。特别是在Pa药丹参汤中口服flor药苷时,pa药苷的t(max),C(max)和AUC的参数显着增加(P <0.05,P <0.001)。 ),V药(Ve)和丹参汤相比,V(d)和CL降低(P <0.05或P <0.01)。

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