Häring N, Salama Z, Todesko L, Jaeger H
Analytical Research Centre, LAB GmbH, Neu-Ulm, Fed. Rep. of Germany.
Arzneimittelforschung. 1987 Dec;37(12):1402-4.
An improved gas chromatographic-mass spectrometric chemical ionization assay for the quantitative determination of haloperidol in body fluids is presented. A fused silica, bonded phase capillary column, combined with negative ion chemical ionization (NICI), ammonia as a selective reagent gas and the monitoring of preselected characteristic ions (SIM), provide the combined sensitivity and selectivity necessary for reliable measurements in the low ng/ml range. The lower limit of detection was 0.1 ng/ml plasma and the calibration curve linear in the measured range of 0.1-5 ng/ml. In combination with the excellent imprecision and inaccuracy data and a recovery exceeding 90%, the method is very well suited for quantitative determinations of plasma samples generated during clinical studies, e.g. evaluating the pharmacokinetics and/or bioavailability/bioequivalence of haloperidol.
本文介绍了一种改进的气相色谱 - 质谱化学电离分析法,用于定量测定体液中的氟哌啶醇。熔融石英键合相毛细管柱,结合负离子化学电离(NICI)、氨气作为选择性反应气以及对预选特征离子的监测(SIM),提供了在低纳克/毫升范围内进行可靠测量所需的灵敏度和选择性。检测下限为0.1纳克/毫升血浆,校准曲线在0.1 - 5纳克/毫升的测量范围内呈线性。结合出色的精密度和准确度数据以及超过90%的回收率,该方法非常适合临床研究中产生的血浆样品的定量测定,例如评估氟哌啶醇的药代动力学和/或生物利用度/生物等效性。