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Pharmacokinetics and oral bioavailability studies of three saikogenins in rats using a validated UFLC-MS/MS method

机译:使用验证的UFLC-MS / MS方法对三种索昔甙的药代动力学和口服生物利用度研究

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摘要

Radix Bupleuri (RB) has been widely used in Traditional Chinese Medicine with a long history. Saikosaponins (SSs), the major constituents of RB, are assumed to be transformed into saikogenins (SGs) by human intestinal microflora prior to absorption and then exert pharmacological effects. There have been detailed reports on the deglycosylation of SSs in the gastrointestinal tract. But to date, there is very limited research addressing the further absorption, distribution, metabolism, and excretion of these deglycosylated derivatives in vivo. In this study, a rapid UFLC-MS/MS method was established and fully validated for simultaneously determining four SGs (SGF, SGA, SGD, and SGG) in rat plasma. The developed method was successfully applied to the pharmacokinetics of three SGs (SGF, SGD, and SGG) in rats after oral and intravenous administrations. Finally, the absolute bioavailabilities were calculated at 0.71% for SGF and 0.66% for SGD. However, the oral bioavailability of SGG was not obtained due to the extremely poor absorption in rats.
机译:Radix Bupleuri(RB)已广泛用于中药,历史悠久。索科康康蛋白(SSS)是RB的主要成分,假设在吸收之前通过人肠道微生物群体转化为Saikogenins(SGS),然后施加药理学效应。已经详细报道了胃肠道中SSS的脱糖基化。但到目前为止,研究了解决了这些脱糖基化衍生物在体内的进一步吸收,分布,代谢和排泄的研究非常有限。在该研究中,建立了快速的UFLC-MS / MS方法,并完全验证,用于在大鼠等离子体中同时测定四个SGS(SGF,SGA,SGD和SGD)。在口服和静脉内给药后的大鼠中成功地将开发方法应用于三个SGS(SGF,SGD和SGG)的药代动力学。最后,对于SGF的0.71%计算绝对的生物杀虫性,SGD为0.66%。然而,由于大鼠的吸收极差,因此未获得SGG的口腔生物利用度。

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