首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Study on the pharmacokinetics profiles of Polyphyllin I and its bioavailability enhancement through co-administration with P-glycoprotein inhibitors by LC-MS/MS method
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Study on the pharmacokinetics profiles of Polyphyllin I and its bioavailability enhancement through co-administration with P-glycoprotein inhibitors by LC-MS/MS method

机译:通过LC-MS / MS方法与P-糖蛋白抑制剂并用可提高多叶绿素I的药代动力学特征及其生物利用度

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摘要

Polyphyllin I (PPI), one of the steroidal saponins in Paris polyphylla, is a promising natural anticancer candidate. Although the anticancer activity of PPI has been well demonstrated, information regarding the pharmacokinetics and bioavailability is limited. In this study, a series of reliable and rapid liquid chromatography-tandem mass spectrometry methods were developed and successfully applied to determinate PPI in rat plasma, cell incubation media and cell homogenate. Then the pharmacokinetics of PPI in rats was studied and the result revealed that PPI was slowly eliminated with low oral bioavailability (about 0.62%) at a dose of 50 mg/1
机译:Polyphyllin I(PPI)是巴黎多叶植物中的甾体皂苷之一,是一种很有前途的天然抗癌候选药物。尽管已经很好地证明了PPI的抗癌活性,但是有关药代动力学和生物利用度的信息仍然有限。在这项研究中,开发了一系列可靠,快速的液相色谱-串联质谱方法,并将其成功地用于测定大鼠血浆,细胞培养介质和细胞匀浆中的PPI。然后研究了PPI在大鼠中的药代动力学,结果表明,以50 mg / 1

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