Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, Iran.
J Chromatogr A. 2012 Jul 27;1248:24-31. doi: 10.1016/j.chroma.2012.05.085. Epub 2012 May 31.
In this study, a developed technique was reported for extraction and pre-concentration of methamphetamine (MAMP) and 3,4-methylenedioxymethamphetamine (MDMA, ecstasy) from urine samples using molecularly imprinted-solid phase extraction (MISPE) along with simultaneous derivatization and dispersive liquid-liquid microextraction (DLLME). Molecularly imprinted microspheres as sorbent in solid phase extraction (SPE) procedure were synthesized using precipitation polymerization with MAMP as the template. Aqueous solution of the target analytes was passed through MAMP-MIP cartridge and the adsorbed analytes were then eluted with methanol. The collected eluate was mixed with butylchloroformate which served as the derivatization reagent as well as the extraction solvent. The mixture was immediately injected into deionized water. After centrifugation, 1 μL of the settled organic phase was injected into gas chromatography-flame ionization detection (GC-FID) or gas chromatography-mass spectrometry (GC-MS). Various experimental parameters affecting the performance of both of the steps (MISPE and DLLME) were thoroughly investigated. The calibration graphs were linear in the ranges of 10-1500 ng mL(-1) (MAMP) and 50-1500 ng mL(-1) (MDMA), and the detection limits (LODs) were 2 and 18 ng mL(-1), respectively. The relative standard deviations (%RSDs) obtained for six repeated experiments (100 ng mL(-1) of each drug) were 5.1% and 6.8% for MAMP and MDMA, respectively. The relative recoveries obtained for the analytes in human urine samples, spiked with different levels of each drug, were within the range of 80-88%.
在这项研究中,报道了一种从尿液样品中提取和预浓缩甲基苯丙胺(MAMP)和 3,4-亚甲二氧基甲基苯丙胺(MDMA,摇头丸)的方法,使用分子印迹固相萃取(MISPE)和同时衍生化和分散液 - 液微萃取(DLLME)。分子印迹微球作为固相萃取(SPE)过程中的吸附剂,是通过沉淀聚合以 MAMP 为模板合成的。将目标分析物的水溶液通过 MAMP-MIP 小柱,然后用甲醇洗脱吸附的分析物。收集的洗脱液与丁基氯甲酸酯混合,丁基氯甲酸酯既是衍生化试剂,也是萃取溶剂。混合物立即注入去离子水。离心后,将 1 μL 沉降的有机相注入气相色谱 - 火焰离子化检测(GC-FID)或气相色谱 - 质谱(GC-MS)。彻底研究了影响两个步骤(MISPE 和 DLLME)性能的各种实验参数。校准曲线在 10-1500 ng mL(-1)(MAMP)和 50-1500 ng mL(-1)(MDMA)范围内呈线性,检测限(LOD)分别为 2 和 18 ng mL(-1)。对于六个重复实验(每种药物 100 ng mL(-1)),MAMP 和 MDMA 的相对标准偏差(%RSD)分别为 5.1%和 6.8%。在人尿液样品中,加入不同水平的每种药物,分析物的相对回收率在 80-88%范围内。