Chemistry Department, Federal University of São Carlos, São Carlos, SP, Brazil.
J Chromatogr B Analyt Technol Biomed Life Sci. 2012 Mar 15;889-890:17-23. doi: 10.1016/j.jchromb.2012.01.021. Epub 2012 Jan 30.
This work reports the use of a liquid chromatography ion trap tandem mass spectrometry (LC-IT-MS/MS) system for quantification in human milk samples of both carbamazepine (CBZ) and its active metabolite, carbamazepine 10,11-epoxide (CBZE). An octadecyl restricted-access media bovine serum albumin column (RAM-BSA C(18)) was used in single-column mode. Selectivity, extraction efficiency, accuracy and precision were achieved employing 100 μL of the sample, without preparation, with detection limits of 20.0 ng/mL for CBZ and 40.0 ng/mL for CBZE. The matrix effect was investigated for the compounds by post-column infusion (qualitative) and by on-line extraction (quantitative). It was observed suppression effect for CBZ and CBZE by post-column infusion, ion suppression of 0.80 for CBZ, and enhancement of 1.28 for CBZE by on-line extraction. The developed method was validated and applied to analyze breast milk samples from one nursing mother. CBZ and CBZE were quantified in the concentrations of 2.26 μg/mL and 1.54 μg/mL, respectively. To our knowledge, this is the first report on the simultaneous determination of CBZ and its active metabolite by direct injection of human milk serum.
本工作报道了一种液相色谱-离子阱串联质谱(LC-IT-MS/MS)系统,用于在人乳样品中同时定量测定卡马西平(CBZ)及其活性代谢物 10,11-环氧化物(CBZE)。采用单柱模式的十八烷基受限-access 介质牛血清白蛋白柱(RAM-BSA C(18))。采用 100 μL 未经预处理的样品,通过柱后注入(定性)和在线提取(定量)考察了化合物的选择性、提取效率、准确度和精密度,检测限分别为 CBZ 20.0 ng/mL 和 CBZE 40.0 ng/mL。通过柱后注入进行了化合物的基质效应考察,观察到 CBZ 和 CBZE 的抑制效应,CBZ 的离子抑制为 0.80,在线提取时 CBZE 的增强为 1.28。所建立的方法经过验证后,应用于人乳样本的分析。从一位哺乳期母亲的样本中分别定量检测到 CBZ 和 CBZE 的浓度为 2.26 μg/mL 和 1.54 μg/mL。据我们所知,这是首次报道直接进样人乳血清同时测定 CBZ 和其活性代谢物。