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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Molecularly imprinted-solid phase extraction combined with simultaneous derivatization and dispersive liquid-liquid microextraction for selective extraction and preconcentration of methamphetamine and ecstasy from urine samples followed by gas chromatography
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Molecularly imprinted-solid phase extraction combined with simultaneous derivatization and dispersive liquid-liquid microextraction for selective extraction and preconcentration of methamphetamine and ecstasy from urine samples followed by gas chromatography

机译:分子印迹固相萃取与同时衍生化和液-液分散微萃取相结合,用于从尿液样品中选择性提取和预浓缩甲基苯丙胺和摇头丸,然后进行气相色谱分析

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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, 1μL 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 10-1500ngmL ~(-1) (MAMP) and 50-1500ngmL ~(-1) (MDMA), and the detection limits (LODs) were 2 and 18ngmL ~(-1), respectively. The relative standard deviations (%RSDs) obtained for six repeated experiments (100ngmL ~(-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%.
机译:在这项研究中,报道了一种开发的技术,该技术使用分子印迹固相萃取(MISPE)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),同时进行衍生化和分散液-液微萃取(DLLME)。以MAMP为模板,采用沉淀聚合法合成了固相萃取(SPE)过程中作为吸附剂的分子印迹微球。将目标分析物的水溶液通过MAMP-MIP色谱柱,然后用甲醇洗脱吸附的分析物。将收集的洗脱液与用作衍生试剂的氯甲酸丁酯和萃取溶剂混合。将混合物立即注入去离子水中。离心后,将1μL沉淀的有机相注入气相色谱-火焰电离检测(GC-FID)或气相色谱-质谱(GC-MS)中。彻底研究了影响两个步骤(MISPE和DLLME)性能的各种实验参数。校正曲线在10-1500ngmL〜(-1)(MAMP)和50-1500ngmL〜(-1)(MDMA)范围内呈线性,检出限(LOD)为2和18ngmL〜(-1),分别。通过六个重复实验(每种药物100ngmL〜(-1))获得的相对标准偏差(MRS和MDMA)分别为5.1%和6.8%。人体尿液样品中分析物的相对回收率(以每种药物的不同含量加标)在80-88%的范围内。

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