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High-throughput and simultaneous analysis of eight central-acting muscle relaxants in human plasma by ultra-performance liquid chromatography–tandem mass spectrometry in the positive and negative ionization modes

机译:高效液相色谱-串联质谱法在正离子和负离子模式下对人血浆中的八种中枢作用肌肉松弛剂进行高通量同时分析

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In this report, a high-throughput and sensitive method for analysis of eight central-acting muscle relaxants in human plasma by ultra-performance liquid chromatography–tandem mass spectrometry (UPLC-MS/MS) in the positive and negative ionization modes using tolbutamide as internal standard is presented. After pretreatment of a plasma sample by solid-phase extraction with an Oasis HLB cartridge, muscle relaxants were analyzed by UPLC with Acquity UPLC BEH C18 column and Acquity TQD tandem quadrupole mass spectrometer equipped with an electrospray ionization interface. The calibration curves for muscle relaxants spiked into human plasma equally showed good linearities in the nanogram per milliliter order range. The detection limits (signal-to-noise ratio = 3) was as low as 0.1–2 ng/mL. The method gave satisfactory recovery rates, accuracy, and precision for quality control samples spiked with muscle relaxants. To further validate the present method, 250 mg of chlorphenesin carbamate was orally administered to a healthy male volunteer, and the concentrations of chlorphenesin carbamate in plasma were measured 0.5, 1, 2, 4, 6, and 8 h after dosing; their concentrations in human plasma were between 0.62 and 2.44 μg/mL. To our knowledge, this is the first report describing simultaneous analysis of over more than two central-acting muscle relaxants by liquid chromatography–tandem mass spectrometry. This has been realized by the capability of our instrument for simultaneous multiple reaction monitoring of the target compounds in both positive and negative ionization modes. Therefore, the present method seems very useful in forensic and clinical toxicology and pharmacokinetic studies.
机译:在本报告中,采用高效液相色谱-串联质谱(UPLC-MS / MS),采用甲苯磺丁酰胺作为正离子和负离子化模式,以高通量和灵敏的方法分析人血浆中的八种中枢作用肌肉松弛剂。提出内部标准。在使用Oasis HLB柱通过固相萃取对血浆样品进行预处理之后,使用配备有电喷雾电离接口的Acquity UPLC BEH C 18 色谱柱和Acquity TQD串联四极质谱仪通过UPLC分析肌肉松弛剂。 。掺入人血浆中的肌肉松弛剂的校准曲线同样显示出纳克/毫升量级范围内的良好线性。检出限(信噪比= 3)低至0.1–2 ng / mL。该方法为掺入肌肉松弛剂的质量控制样品提供了令​​人满意的回收率,准确度和精密度。为了进一步验证本方法,向健康的男性志愿者口服250毫克氨基酚氯苯甲酸酯,并在给药后0.5、1、2、4、6和8小时测量血浆中氨基甲酸氯苯酚的浓度。它们在人血浆中的浓度在0.62至2.44μg/ mL之间。据我们所知,这是第一份报告,描述了通过液相色谱-串联质谱法同时分析两种以上的中枢作用肌肉松弛剂。这已经通过我们的仪器在正电离和负电离模式下同时监测目标化合物的多反应能力实现了。因此,本方法在法医和临床毒理学以及药代动力学研究中似乎非常有用。

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