首页> 外文期刊>Journal of Analytical Toxicology >Screening procedure for detection of dihydropyridine calcium channel blocker metabolites in urine as part of a systematic toxicological analysis procedure for acidic compounds by gas chromatography-mass spectrometry after extractive methylation.
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Screening procedure for detection of dihydropyridine calcium channel blocker metabolites in urine as part of a systematic toxicological analysis procedure for acidic compounds by gas chromatography-mass spectrometry after extractive methylation.

机译:萃取甲基化后通过气相色谱-质谱法对酸性化合物进行系统毒理学分析的一部分,用于检测尿液中二氢吡啶钙通道阻滞剂代谢物的筛选程序。

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摘要

A gas chromatographic-mass spectrometric (GC-MS) screening procedure was developed for the detection of dihydropyridine calcium channel blocker ("calcium antagonist") metabolites in urine as part of a systematic toxicological analysis procedure for acidic drugs and poisons after extractive methylation. The part of the phase-transfer catalyst remaining in the organic phase was removed by solid-phase extraction on a diol phase. The compounds were separated by capillary GC and identified by computerized MS in the full scan mode. Using mass chromatography with the ions m/z 139, 284, 297, 298, 310, 312, 313, 318, 324, and 332, the possible presence of calcium channel blocker metabolites could be indicated. The identity of positive signals in such mass chromatograms was confirmed by comparison of the peaks underlying full mass spectra with the reference spectra recorded during this study. This method allowed the detection of therapeutic concentrations of amlodipine, felodipine, isradipine, nifedipine, nilvadipine, nimodipine, nisoldipine, and nitrendipine in human urine samples. Because urine samples from patients treated with nicardipine were not available, the detection of nicardipine in rat urine was studied. The overall recovery ranged between 67 and 77% with a coefficient of variation of less than 10%, and the limit of detection was at least 10 ng/mL (signal-to-noise ratio = 3) in the full-scan mode.
机译:开发了一种气相色谱-质谱(GC-MS)筛选方法,用于检测尿液中的二氢吡啶钙通道阻滞剂(“钙拮抗剂”)代谢物,这是萃取性甲基化后酸性药物和毒物的系统毒理学分析程序的一部分。通过在二醇相上进行固相萃取,除去残留在有机相中的部分相转移催化剂。通过毛细管GC分离化合物,并通过计算机MS在全扫描模式下进行鉴定。使用质谱法对离子m / z 139、284、297、298、310、312、313、318、324和332进行分析,可以表明存在钙通道阻滞剂代谢物。通过比较整个质谱下面的峰与本研究中记录的参考质谱图,可以确认此类质谱图中阳性信号的身份。该方法可以检测人尿液样品中氨氯地平,非洛地平,伊拉地平,硝苯地平,尼伐地平,尼莫地平,尼索地平和尼群地平的治疗浓度。由于无法获得尼卡地平治疗患者的尿液样本,因此研究了大鼠尿液中尼卡地平的检测。在全扫描模式下,总回收率在67%到77%之间,变异系数小于10%,检出限至少为10 ng / mL(信噪比= 3)。

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