首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of pimpinellin, isopimpinellin and phellopterin in rat plasma by a validated UPLC-MS/MS and its application to a pharmacokinetic study after administration of Toddalia asiatica extract
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Simultaneous determination of pimpinellin, isopimpinellin and phellopterin in rat plasma by a validated UPLC-MS/MS and its application to a pharmacokinetic study after administration of Toddalia asiatica extract

机译:经验证的UPLC-MS / MS同时测定大鼠血浆中的匹品松林,异匹品松林和鞘翅磷脂,并将其应用于积雪草提取物后的药代动力学研究

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摘要

A rapid and selective ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed for simultaneous determination of three bioactive coumarins of Toddalia asiatica extract including pimpinellin, isopimpinellin and phellopterin in rat plasma for the first time. Phenacetin was used as the internal standard (IS). Plasma samples were extracted by liquid-liquid extraction with methyl tert-butyl ether. The chromatographic separation was carried out on an ACQUITY UPLC? BEH C _(18) column with an isocratic mobile phase consisting of methanol-5mmol/L ammonium acetate (65:35, v/v). The detection was performed on a triple quadrupole tandem mass spectrometer by multiple reaction monitoring (MRM) via electrospray ionization (ESI) source with positive ionization mode. The method was linear for all analytes over investigated range with all correlation coefficients greater than 0.9942. The lower limits of quantification (LLOQ) were 25.0ng/mL for pimpinellin, 10.0ng/mL for isopimpinellin and 5.00ng/mL for phellopterin. The intra- and inter-day precision (RSD%) was within 12% and the accuracy (RE%) ranged from -2.3% to 5.5%. The rapid and sensitive method was fully validated and successfully applied to the pharmacokinetic study of pimpinellin, isopimpinellin and phellopterin in rats following oral administration of Toddalia asiatica extract.
机译:建立了一种快速,选择性的超高效液相色谱-串联质谱(UPLC-MS / MS)方法,用于首次同时测定大鼠血浆中积雪草提取物的三种生物活性香豆素,其中包括匹品林,异匹品林和鞘磷脂。非那西丁用作内标(IS)。用甲基叔丁基醚通过液-液萃取来萃取血浆样品。色谱分离是在ACQUITY UPLC?上进行的。 BEH C_(18)柱,其等度流动相为甲醇-5mmol / L乙酸铵(65:35,v / v)。通过多反应监测(MRM)通过正电离模式下的电喷雾电离(ESI)源在三重四极杆串联质谱仪上进行检测。该方法对于研究范围内的所有分析物都是线性的,所有相关系数均大于0.9942。吡虫啉的定量下限(LLOQ)为25.0ng / mL,异氯吡林为10.0ng / mL,而蝶呤为5.00ng / mL。日内和日间精度(RSD%)在12%以内,精度(RE%)在-2.3%至5.5%的范围内。该快速灵敏的方法得到了充分验证,并成功地应用于口服积雪草提取物中的吡虫啉,异吡虫啉和鞘翅磷脂的药代动力学研究。

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