首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Pharmacokinetic comparisons of puerarin, daidzin and the glucuronide metabolite of puerarin after administration of total flavonoid from Gegen alone and total flavonoid from Gegen combined with total saponin from Sanqi in rats under different physiological states
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Pharmacokinetic comparisons of puerarin, daidzin and the glucuronide metabolite of puerarin after administration of total flavonoid from Gegen alone and total flavonoid from Gegen combined with total saponin from Sanqi in rats under different physiological states

机译:葛根总黄酮,葛根总黄酮与三七总皂苷联合给药后不同生理状态下葛根素,大豆苷和葛根素的代谢动力学比较

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Gegen is one of the most commonly used traditional Chinese medicines for promoting blood circulation and removing blood stasis. Puerarin and daidzin are the main active constituents of Gegen. Puerarin is mainly metabolized in rats by glucuronidation and the major metabolite from rat urine has been identified as puerarin-7-O-glucuronide through semi-preparative HPLC isolation and then spectroscopic analysis. The study investigated the pharmacokinetic behavior of puerarin-7-. O-glucuronide (without enzymatic hydrolysis), puerarin and daidzin when total flavonoid from Gegen was administered in normal and blood stasis animals or in blood stasis animals alone or in combination with Sanqi. The plasma samples were processed by protein precipitation with methanol, and chromatographed on a Thermo Syncronis C18 column (10. cm. ×. 2.1. mm, 1.7. μm) by gradient elution at a flow rate of 0.25. mL/min, and detected with a triple quadrupole tandem mass spectrometer by selected reaction monitoring via electrospray ionization source with positive ionization mode. An unpaired Student's t-test was used for the statistical comparison of the main pharmacokinetic parameters. There were statistically significant differences (P<. 0.05) in the pharmacokinetic parameters of puerarin-7-. O-glucuronide, puerarin and daidzin involving the AUC, CL and Vd not only between normal rats and blood stasis rats after administration of total flavonoid from Gegen, but also between administration of total flavonoid from Gegen alone and in combination with total saponin from Sanqi in blood stasis rats. The results obtained suggest that the pharmacokinetic behavior of puerarin-7-. O-glucuronide, puerarin and daidzin are changed when total flavonoid from Gegen was administered in blood stasis animals or in combination with total saponin from Sanqi.
机译:葛根是促进血液循环和祛瘀的最常用中药之一。葛根素和大豆苷是葛根的主要活性成分。葛根素主要通过葡萄糖醛酸化在大鼠中代谢,并且通过半制备型HPLC分离然后进行光谱分析,大鼠尿液中的主要代谢物已被确定为葛根素7-O-葡萄糖醛酸。该研究调查了葛根素7-的药代动力学行为。在正常和血瘀动物中,或在血瘀动物中单独或与三七合用时,给予Gegen总黄酮时的O-葡萄糖醛酸苷(无酶水解),葛根素和大豆苷。血浆样品用甲醇进行蛋白沉淀处理,并在Thermo Syncronis C18色谱柱(10.cm.×.2.1.mm,1.7.μm)上进行色谱分离,流速为0.25。 mL / min,并使用三重四极杆串联质谱仪通过正电离模式下的电喷雾电离源通过选定的反应监测进行检测。未配对的学生t检验用于主要药代动力学参数的统计比较。葛根素7-的药代动力学参数有统计学上的显着差异(P <0.05)。 O-葡萄糖醛酸,葛根素和黄豆苷不仅涉及葛根总黄酮在正常大鼠和血瘀大鼠之间的AUC,CL和Vd,而且在单独施用葛根总黄酮和与三七总皂苷联合给药之间血瘀大鼠。获得的结果表明葛根素7-的药代动力学行为。当在血瘀动物中或与三七总皂苷组合使用葛根总黄酮时,O-葡萄糖醛酸苷,葛根素和大豆苷会改变。

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