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Nuciferine is an important drug candidate for the treatment of obesity-related diseases. However, few investigations have been conducted about the pharmacokinetics and tissue distribution of nuciferine to better understand its behavior and action mechanism in vivo. Thus, a sensitive and reliable liquid chromatography with tandem mass spectrometry (HPLC-MS/MS) method was established and validated for the quantification of nuciferine in rat plasma and tissue samples. The validated method was successfully applied to the pharmacokinetic and tissue distribution study of nuciferine in rats. One-compartmental pharmacokinetic parameters indicated that nuciferine had rapid distribution, extensive tissue uptake, and poor absorption into systemic circulation. The values of absolute bioavailability were (3.8±1.4)

作者:Shengying, Gu;Guanhua, Zhu;Yuzhu, Wang;Qin, Li;Xin, Wu;Jigang, Zhang;Gaolin, Liu;Xiaoyu, Li

来源:Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 2014 年 961卷

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作者:
Shengying, Gu;Guanhua, Zhu;Yuzhu, Wang;Qin, Li;Xin, Wu;Jigang, Zhang;Gaolin, Liu;Xiaoyu, Li
来源:
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 2014 年 961卷
标签:
LC–MS/MS Nuciferine Pharmacokinetics Tissue distribution
Nuciferine is an important drug candidate for the treatment of obesity-related diseases. However, few investigations have been conducted about the pharmacokinetics and tissue distribution of nuciferine to better understand its behavior and action mechanism in vivo. Thus, a sensitive and reliable liquid chromatography with tandem mass spectrometry (HPLC-MS/MS) method was established and validated for the quantification of nuciferine in rat plasma and tissue samples. The validated method was successfully applied to the pharmacokinetic and tissue distribution study of nuciferine in rats. One-compartmental pharmacokinetic parameters indicated that nuciferine had rapid distribution, extensive tissue uptake, and poor absorption into systemic circulation. The values of absolute bioavailability were (3.8±1.4)

相似文献