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Simultaneous quantification of ginsenoside Rg1 and its metabolites by HPLC–MS/MS:Rg1 excretion in rat bile, urine and feces

机译:通过HPLC-MS / MS:Rg1排泄大鼠胆汁,尿液和粪便中人参皂苷Rg1及其代谢物的同时定量

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摘要

Ginsenoside Rg1(Rg1), the major effective component of ginseng, has been shown to have multiple bioactivities, but low oral bioavailability. The aim of this study was to develop a simple, sensitive and rapid high performance liquid chromatography–tandem mass spectrometry(LC–MS/MS) method, which could be used to validate and quantify the concentrations of Rg1 and its metabolites in Sprague-Dawley rat bile,urine, and feces after oral administration(25 mg/kg). Calibration curves offered satisfactory linearity(r40.995)within the determined ranges. Both intra-day and inter-day variances were less than 15%, and the accuracy was within 80–120%. The excretion recoveries of Rg1, ginsenoside Rh1(Rh1), and protopanaxatriol(Ppt) in bile,urine, and feces combined were all greater than 70%. The fecal excretion recoveries of Rg1, Rh1, and Ppt were40.11%, 22.19%, and 22.88%, respectively, whereas 6.88% of Rg1 and 0.09% of Rh1 were excreted in bile.Urinary excretion accounted for only 0.04% of Rg1. In conclusion, the observed excretion profiles for Rg1 and its metabolites after oral administration are helpful for understanding the poor oral bioavailability of Rg1 and will aid further investigations of Rg1 as a pharmacologically active component.
机译:人参皂苷Rg1(Rg1)是人参的主要有效成分,已被证明具有多种生物活性,但口服生物利用度较低。这项研究的目的是开发一种简单,灵敏,快速的高效液相色谱-串联质谱(LC-MS / MS)方法,该方法可用于验证和定量Sprague-Dawley中Rg1及其代谢物的浓度。口服后大鼠胆汁,尿液和粪便(25 mg / kg)。在确定的范围内,校准曲线提供了令人满意的线性度(r40.995)。日内和日间方差均小于15%,准确度在80-120%之内。在胆汁,尿液和粪便中,Rg1,人参皂苷Rh1(Rh1)和原托那三醇(Ppt)的排泄回收率均大于70%。 Rg1,Rh1和Ppt的粪便排泄回收率分别为40.11%,22.19%和22.88%,而Rg1的6.88%和Rh1的0.09%排泄在胆汁中,尿液的排泄仅占Rg1的0.04%。总之,口服后观察到的Rg1及其代谢产物的排泄曲线有助于理解Rg1不良的口服生物利用度,并将有助于进一步研究Rg1作为药理活性成分。

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