Department of Chemistry, Faculty of Science, Ilam University, Ilam, Iran.
Department of Chemistry, Faculty of Science, Ilam University, Ilam, Iran.
J Chromatogr A. 2021 Oct 11;1655:462500. doi: 10.1016/j.chroma.2021.462500. Epub 2021 Aug 28.
We here present an efficient approach for the tandem extraction of psychotropic drugs using biodegradable materials. In this regard, gel electromembrane extraction (G-EME) was combined with the emulsification-based microextraction (ME) technique by rhamnolipid bioaggregates as a green extraction approach. The tandem extraction technique consists of two stages: (i) extraction of psychotropic drugs from human urine samples to the acceptor phase situated on the other side of the agarose gel membrane, and (ii) transfer of analytes from the acceptor phase into a colloidal phase of rhamnolipid biosurfactants. The colloidal phase was formed by adding rhamnolipid biosurfactants to the extracted phase of the first step. The colloidal phase was finally injected into a liquid chromatographic system for quantitative analysis. G-EME mechanism is based on electrokinetic migration of charged species toward oppositely charged electrode located in the acceptor solution under the influence of the electric field. After extraction, the analytes were trapped in an emulsion phase floating on the surface of the solution and at the end were injected into the liquid chromatographic system. The method provided good linearity in the ranges of 5-100 and 10-100 μg. L for methamphetamine and amphetamine, respectively with (r > 0.992). Also, the detection limits (LODs) were 1 and 5 μg. L for methamphetamine and amphetamine, respectively. The mean extraction recoveries by G-EME-ME for real samples at three spiked concentrations were in the range 95.9-101.1% and complete analytical workflow within only 18 min.
我们在此提出了一种使用可生物降解材料串联提取精神药物的有效方法。在这方面,胶束电动膜萃取(G-EME)与基于乳化的微萃取(ME)技术相结合,使用鼠李糖脂生物聚集体作为绿色萃取方法。串联萃取技术包括两个阶段:(i)从人尿样中萃取精神药物到琼脂糖凝胶膜另一侧的接受相,(ii)将分析物从接受相转移到鼠李糖脂生物表面活性剂的胶体相中。胶体相通过向第一步萃取相添加鼠李糖脂生物表面活性剂来形成。最后,将胶体相注入液相色谱系统进行定量分析。G-EME 机制基于在电场的影响下,带电荷物质朝着位于接受溶液中的相反电荷电极的电动迁移。萃取后,分析物被捕获在浮在溶液表面的乳液相中,最后注入液相色谱系统。该方法在甲卡西酮和苯丙胺的浓度范围为 5-100 和 10-100 μg.L 时提供了良好的线性关系(r > 0.992)。此外,甲卡西酮和苯丙胺的检测限(LOD)分别为 1 和 5 μg.L。在三个加标浓度下,通过 G-EME-ME 对实际样品的平均萃取回收率在 95.9-101.1%之间,整个分析工作流程仅需 18 分钟。