首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Development and validation of an LC-MS/MS method for the determination of mesalazine in beagle dog plasma and its application to a pharmacokinetic study
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Development and validation of an LC-MS/MS method for the determination of mesalazine in beagle dog plasma and its application to a pharmacokinetic study

机译:LC-MS / MS法测定比格犬血浆中美沙拉嗪的方法开发与验证及其在药代动力学研究中的应用

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A simple, specific and sensitive LC-MS/MS method was developed and validated for the determination of mesalazine in beagle dog plasma. The plasma samples were prepared by protein precipitation, then the separation of the analyte was achieved on a Waters Spherisorb C-6 column (150x4.6mm, 5 mu m) with a mobile phase consisting of 0.2% formic acid in water-methanol (20:80, v/v). The flow rate was set at 1.0mL/min with a split ratio of 3:2. Mass spectrometric detection was achieved by a triple-quadrupole mass spectrometer equipped with an electrospray source interface in positive ionization mode. Quantitation was performed using selected reaction monitoring of precursor-product ion transitions at m/z 154m/z 108 for mesalazine and m/z 285m/z 193 for diazepam (internal standard). The linear calibration curve of mesalazine was obtained over the concentration range 50-30,000ng/mL. The matrix effect of mesalazine was within +/- 9.8%. The intra- and inter-day precisions were <7.9% and the accuracy (relative error) was within +/- 3.5%. The validated method was successfully applied to investigate the pharmacokinetics of mesalazine in healthy beagle dogs after rectal administration of mesalazine suppository. Copyright (c) 2014 John Wiley & Sons, Ltd.
机译:开发了一种简单,特异性和灵敏的LC-MS / MS方法,并验证了比格犬血浆中美沙拉嗪的含量测定。通过蛋白质沉淀制备血浆样品,然后在Waters Spherisorb C-6色谱柱(150x4.6mm,5μm)上进行分析物分离,流动相由0.2%甲酸的水-甲醇溶液(20 :80,v / v)。流速设定为1.0mL / min,分流比为3:2。质谱检测是通过在正电离模式下配备电喷雾源接口的三重四极杆质谱仪实现的。使用对美沙拉嗪在m / z 154m / z 108和对地西epa m / z 285m / z 193(内标)的前体产物离子跃迁的选定反应监测,进行定量。在50-30,000ng / mL的浓度范围内获得美沙拉嗪的线性校准曲线。美沙拉嗪的基质效应在+/- 9.8%之内。日内和日间精度为<7.9%,精度(相对误差)在+/- 3.5%之内。经验证的方法已成功应用于美沙拉嗪栓剂直肠给药后对健康比格犬的美沙拉嗪的药代动力学研究。版权所有(c)2014 John Wiley&Sons,Ltd.

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