Jeanville P M, Estapé E S, Needham S R, Cole M J
Drug Metabolism Technology Department, Pfizer Inc., Groton, Connecticut 06340, USA.
J Am Soc Mass Spectrom. 2000 Mar;11(3):257-63. doi: 10.1016/S1044-0305(99)00138-5.
A rapid, but sensitive and selective method for confirmation and quantitation of benzoylecgonine (BZE) and cocaine (COC) in urine by fast-gradient liquid chromatography/tandem mass spectrometry (LC/MS/MS) is described. The chromatographic separation was performed on a reversed phase column employing fast-gradient techniques. Matrix prepared standards, blanks, and QC's were filtered then aliquots were transferred into a 96 well plate. Injection volumes of 25 microL were made onto the analytical column, with the flow diverted from the atmospheric pressure ionization source for the first 0.5 min of the analysis. Simultaneous multiple reaction monitoring (MRM) of three discrete transitions for each compound were used to identify BZE and COC. Quantitation was achieved utilizing the most prominent parent-daughter transition and internal standard calibration techniques. The coefficients of variation (CV) for the analysis of these drugs ranged from 0.6% to 6.8% at a concentration of 150 ng/mL (n = 155). This method suggests that fast-gradient LC/MS/MS may be suitable for routine confirmation of immunoassay cocaine-positive samples.
本文描述了一种通过快速梯度液相色谱/串联质谱法(LC/MS/MS)对尿液中苯甲酰爱康宁(BZE)和可卡因(COC)进行确证和定量的快速、灵敏且具选择性的方法。色谱分离在反相柱上采用快速梯度技术进行。将基质制备的标准品、空白样品和质量控制样品过滤后,取等分试样转移至96孔板中。向分析柱注入25微升进样体积,在分析的前0.5分钟将流动相从大气压电离源分流。对每种化合物的三个离散跃迁进行同步多反应监测(MRM)以鉴定BZE和COC。利用最显著的母离子-子离子跃迁和内标校准技术进行定量。在浓度为150纳克/毫升时(n = 155),这些药物分析的变异系数(CV)范围为0.6%至6.8%。该方法表明快速梯度LC/MS/MS可能适用于免疫测定可卡因阳性样品的常规确证。