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Quantification of neomangiferin in rat plasma by liquid chromatography-tandem mass spectrometry and its application to bioavailability study.
Journal of Pharmaceutical Analysis ( IF 6.1 ) Pub Date : 2016-03-28 , DOI: 10.1016/j.jpha.2016.03.005
Bo Yang 1 , Zhirui Liu 1 , Shenglan Shang 1 , Xiaojian Qin 1 , Peiyuan Xia 1
Affiliation  

Neomangiferin, a natural C-glucosyl xanthone, has recently received a great deal of attention due to its multiple biological activities. In this study, a rapid and sensitive ultra-high performance liquid chromatography tandem mass spectrometry (UHPLC–MS/MS) method for the quantification of neomangiferin in rat plasma was developed. Using chloramphenicol as an internal standard (IS), plasma samples were subjected to a direct protein precipitation process using methanol (containing 0.05% formic acid). Quantification was performed by multiple reactions monitoring (MRM) method, with the transitions of the parent ions to the product ions of m/z 583.1→330.9 for NG and m/z 321.1→151.9 for IS. The assay was shown to be linear over the range of 0.2–400 ng/mL, with a lower limit of quantification of 0.2 ng/mL. Mean recovery of neomangiferin in plasma was in the range of 97.76%–101.94%. Relative standard deviations (RSDs) of intra-day and inter-day precision were both <10%. The accuracy of the method ranged from 94.20% to 108.72%. This method was successfully applied to pharmacokinetic study of neomangiferin after intravenous (2 mg/kg) and intragastric (10 mg/kg) administration for the first time. The oral absolute bioavailability of neomangiferin was estimated to be 0.53%±0.08% with an elimination half-life (t1/2) value of 2.74±0.92 h, indicating its poor absorption and/or strong metabolism in vivo.



中文翻译:

液相色谱-串联质谱法定量测定大鼠血浆中的新芒果苷及其在生物利用度研究中的应用。

Neomangiferin,一种天然的C-葡萄糖基yl吨酮,由于其多种生物活性,最近受到了广泛的关注。在这项研究中,开发了一种快速灵敏的超高效液相色谱串联质谱(UHPLC–MS / MS)方法定量大鼠血浆中的新芒果苷。使用氯霉素作为内标(IS),血浆样品使用甲醇(含0.05%甲酸)进行直接蛋白沉淀过程。通过多反应监测(MRM)方法进行定量,其中NG的母离子转变为m / z 583.1→330.9,IS的m / z 321.1→151.9。该分析显示在0.2–400 ng / mL范围内呈线性,定量下限为0.2 ng / mL。血浆新芒果苷的平均回收率在97.76%–101.94%的范围内。日内和日间精度的相对标准偏差(RSD)均<10%。该方法的准确度为94.20%至108.72%。首次静脉注射(2 mg / kg)和胃内注射(10 mg / kg)后,该方法成功应用于新芒果苷的药代动力学研究。新芒果苷的口服绝对生物利用度估计为0.53%±0.08%,消除半衰期(t 该方法成功应用于首次静脉注射(2 mg / kg)和胃内注射(10 mg / kg)的新芒果苷的药代动力学研究。新芒果苷的口服绝对生物利用度估计为0.53%±0.08%,消除半衰期(t 该方法成功应用于首次静脉注射(2 mg / kg)和胃内注射(10 mg / kg)的新芒果苷的药代动力学研究。新芒果苷的口服绝对生物利用度估计为0.53%±0.08%,消除半衰期(t1/2)值为2.74±0.92 h,表明其在体内的吸收不良和/或新陈代谢旺盛。

更新日期:2016-03-28
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