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 >A rapid and sensitive UHPLC-MS/MS method for quantification of 2-(2-hydroxypropanamido) benzoic acid in rat plasma: Application to a pharmacokinetic study
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A rapid and sensitive UHPLC-MS/MS method for quantification of 2-(2-hydroxypropanamido) benzoic acid in rat plasma: Application to a pharmacokinetic study

机译:快速灵敏的UHPLC-MS / MS方法定量测定大鼠血浆中的2-(2-羟基丙酰胺基)苯甲酸:在药代动力学研究中的应用

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摘要

A rapid, sensitive and high throughput UHPLC-MS/MS method was established and validated to assay the concentration of 2-(2-hydroxypropanamido) benzoic acid (HPABA), a promising anti-inflammatory drug, in rat plasma. Plasma samples were processed by liquid-liquid extraction with ethyl acetate and separated on a Shim-pack XR-ODS C_(18) column (75 mm x 3.0 mm, 2.2 |xm) at an isocratic flow rate of 0.4mL/min using acetonitrile-0.1% formic acid in water (50:50, vfv) as mobile phase, and total run time was 2 min. MS/MS detection was accomplished in multiple reaction monitoring (MRM) mode with positive electro-spray ionization. The calibration curve was linear over the concentration range of 0.01-50 |xg/mL with lower limit of quantification of 0.01 mug/mL The intra- and inter-day precisions were below 8.5% in terms of relative standard deviation (RSD), and the accuracy was within ±4.0% in terms of relative error (RE). Extraction recovery, matrix effect and stability were satisfactory in rat plasma. The developed method was successfully applied to a pharmacokinetic study of HPABA following intragastric administration of 25, 50,100 mg/kg and an intravenous injection at a dose of 12.5 mg/kg to Sprague-Dawley rats. Results indicated that HPABA had linear pharmacokinetic properties within the tested intragastric dosage range and the absolute bioavailability was above 59.1%.
机译:建立了快速,灵敏和高通量的UHPLC-MS / MS方法,并验证了该方法可用于测定大鼠血浆中2-(2-羟基丙酰胺基)苯甲酸(HPABA)的浓度,这是一种很有前途的抗炎药。血浆样品通过乙酸乙酯进行液-液萃取处理,并在Shim-pack XR-ODS C_(18)色谱柱(75 mm x 3.0 mm,2.2 | xm)上使用乙腈以0.4mL / min的等度流速分离。 -0.1%甲酸的水溶液(50:50,vfv)作为流动相,总运行时间为2分钟。 MS / MS检测是在带有正电喷雾电离的多反应监测(MRM)模式下完成的。在0.01-50 | xg / mL的浓度范围内,校准曲线是线性的,而定量下限为0.01 mug / mL。就相对标准偏差(RSD)而言,日内和日间精度低于8.5%,并且相对误差(RE)的准确性在±4.0%以内。在大鼠血浆中的提取回收率,基质效应和稳定性令人满意。在胃内给药25、50,100 mg / kg并以12.5 mg / kg的剂量静脉内注射给Sprague-Dawley大鼠后,该开发的方法已成功应用于HPABA的药代动力学研究。结果表明,HPABA在测试的胃内剂量范围内具有线性药代动力学特性,绝对生物利用度高于59.1%。

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