Chen Chung-Yu, Shen Chien-Chun, Yang Tzung-Jie, Chang Yan-Zin, Lee Maw-Rong
Department of Chemistry, National Chung Hsing University, Taichung, Taiwan, ROC.
Talanta. 2009 Feb 15;77(4):1351-7. doi: 10.1016/j.talanta.2008.09.017. Epub 2008 Sep 18.
An integrated method of liquid chromatography-heated electrospray ionization/tandem mass spectrometry was evaluated for high throughput screening of various abused drugs in urine. Chromatographic analysis was performed on a C18 reverse phase column using a linear gradient of 10mM ammonium acetate containing 0.1% formic acid-methanol as mobile phase and the total separation time was 7 min. A simple and rapid sample preparation method used was by passing urine samples through a 0.22 microm PVDF syringe filter. The detection limits of the studied abused drugs in urine were from 0.6 ng mL(-1) (ketamine) to 9.0 ng mL(-1) (norcodeine). According to the results, the linear range was from 1 to 1200 ng mL(-1) with relative standard deviation (R.S.D.s) value below 14.8% (intra-day) and 24.6% (inter-day). The feasibility of applying the proposed method to determine various abused drugs in real samples was examined by analyzing urine samples from drug-abused suspects. The abused drugs including ketamines and amphetamines were detected in suspected urine samples. The results demonstrate the suitability of LC-HESI-MS/MS for high throughput screening of the various abused drugs in urine.
评估了一种液相色谱-加热电喷雾电离/串联质谱联用的综合方法,用于尿液中多种滥用药物的高通量筛查。在C18反相柱上进行色谱分析,以含0.1%甲酸的10mM醋酸铵-甲醇线性梯度溶液为流动相,总分离时间为7分钟。所采用的简单快速的样品制备方法是将尿液样品通过0.22微米的聚偏氟乙烯注射器滤膜。尿液中所研究的滥用药物的检测限为0.6 ng mL-1(氯胺酮)至9.0 ng mL-1(去甲可待因)。结果表明,线性范围为1至1200 ng mL-1,相对标准偏差(R.S.D.s)值日内低于14.8%,日间低于24.6%。通过分析吸毒嫌疑人的尿液样本,检验了应用该方法测定实际样本中多种滥用药物的可行性。在可疑尿液样本中检测到了包括氯胺酮和苯丙胺在内的滥用药物。结果证明了液相色谱-加热电喷雾电离串联质谱联用技术适用于尿液中多种滥用药物的高通量筛查。