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Development of aLiquid-Liquid Microextraction Method Based on aSwitchable Hydrophilicity Solvent for the Simultaneous Determination of 11 Drugs in Urine by GC-MS

机译:基于缺陷亲水性溶剂的异丙液微萃取方法的发展,GC-MS在尿液中同时测定11种药物

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A new and green liquid-liquid microextraction method based on aswitchable hydrophilicity solvent for thedetermination of 11 drugs in urine is presented for the first time. The protonated N,N-dimethylcyclohexylamine was used as an extraction solvent and sodium hydroxide was injected as a trigger for organic-phase separation. The extraction procedure has been optimized and investigated in this study. The intraday and interday recovery ranged from 73.8 to 103.0% and the relative standard deviations were in the range from 2.2 to 13.5% (n=5). The linear range was from 5.0 to 2000.0 mu g L-1, and R-2 wasgreater than 0.99, and the limit of detection was in the range from 0.36 to 12.50 mu g L-1. The proposed method may be a useful procedure for the determination of 11 drugs in urine, and easily incorporated into routine testing for a laboratory.
机译:首次介绍了一种基于缺陷的亲水性溶剂的新的和绿色液体微萃取方法,其尿液中11种药物中的11种药物。 质子化的N,N-二甲基环己酰胺用作萃取溶剂,并注射氢氧化钠作为有机相分离的触发。 在本研究中已经优化和研究了提取程序。 中间和白天回收率范围为73.8至103.0%,相对标准偏差范围为2.2至13.5%(n = 5)。 线性范围为5.0至2000.0μmgl-1,而R-2瓦尔格计数器比0.99,检测极限在0.36至12.50μmg l-1的范围内。 该方法可以是测定尿液中11种药物的有用方法,并容易地掺入实验室的常规测试中。

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