首页> 外文期刊>Journal of mass spectrometry: JMS >Development and validation of a high-performance liquid chromatography-electrospray ionization-MS/MS method for the simultaneous quantitation of levodopa and carbidopa in human plasma
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Development and validation of a high-performance liquid chromatography-electrospray ionization-MS/MS method for the simultaneous quantitation of levodopa and carbidopa in human plasma

机译:高效液相色谱-电喷雾电离-MS / MS方法的开发和验证,可同时定量人血浆中左旋多巴和卡比多巴

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A sensitive and fast high-performance liquid chromatography-electrospray ionization-MS/MS method for the simultaneous quantitation of levodopa and carbidopa in human plasma was developed and validated. A simple protein precipitation step with perchloric acid was used for the cleanup of plasma, and methyldopa was added as an internal standard. The analyses were carried out using an ACE C_(18) column (50 × 4.6 mm i.d.; 5 μm particle size) and a mobile phase consisting of 0.2% formic acid and acetonitrile (90:10). The triple-quadrupole mass spectrometer equipped with an electrospray source in positive mode was set up in the selective reaction monitoring mode to detect the ion transitions m/z 198.1 ? m/z 107.0, m/z 227.2 ? m/z 181.0, and m/z 212.1 ? m/z 139.2 for levodopa, carbidopa, and methyldopa, respectively. The method was validated and proved to be linear, accurate, and precise over the range 50-5000 ng/mL for levodopa and 3-600 ng/mL for carbidopa. The proposed method was successfully applied in a pharmacokinetic study with a levodopa/carbidopa tablet formulation in healthy volunteers.
机译:建立并验证了同时定量人血浆中左旋多巴和卡比多巴的灵敏,高效液相色谱-电喷雾电离-MS / MS方法。一个简单的用高氯酸沉淀蛋白质的步骤用于血浆的净化,并加入甲基多巴作为内标。使用ACE C_(18)色谱柱(内径50×4.6 mm;粒径5μm)和由0.2%甲酸和乙腈(90:10)组成的流动相进行分析。在选择性反应监测模式下,以正反应模式安装了配备电喷雾源的三重四极杆质谱仪,以检测离子跃迁m / z 198.1? m / z 107.0,m / z 227.2? m / z 181.0和m / z 212.1?左旋多巴,卡比多巴和甲基多巴的m / z 139.2。对该方法进行了验证,证明了该方法的线性,准确度和精密度,左旋多巴为50-5000 ng / mL,卡比多巴为3-600 ng / mL。所提出的方法已成功用于健康志愿者中左旋多巴/卡比多巴片剂的药代动力学研究。

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