Xu Fangmin, Liu Lingyun
Institute of Forensic Science, Public Security Bureau of Jiangyin, Jiangsu, China.
Forensic Sci Res. 2017 Sep 27;4(2):188-194. doi: 10.1080/20961790.2017.1377386. eCollection 2019.
A simple and rapid dispersive liquid-liquid microextraction (DLLME) technique coupled with gas chromatography-ion trap mass spectrometry (GC-MS) was developed for the extraction and analysis of methamphetamine (MA), pethidine (PD), ketamine (KT) and tramadol (TD) from human urine. In this study, different parameters affecting the extraction process such as the type and volume of extraction solvent, type and volume of disperser solvent, extraction time and pH value and salt effect were studied and optimized. Under optimized conditions, the enrichment factor ranged from 185 to 226 and the average recovery ranged from 80.45% to 95.55%. The linear range was 10.0-1000.0 µg/L, the limit of detection and quantitation were in the range 0.43-1.96 µg/L and 1.44-6.53 µg/L, respectively. The relative standard deviations were in the range 1.98%-3.90% ( = 7). The obtained results show that DLLME combined with GC-MS is a fast and simple method for the determination of MA, PD, KT and TD in human urine.
建立了一种简单快速的分散液液微萃取(DLLME)技术结合气相色谱-离子阱质谱(GC-MS)法,用于从人尿中萃取和分析甲基苯丙胺(MA)、哌替啶(PD)、氯胺酮(KT)和曲马多(TD)。本研究考察并优化了影响萃取过程的不同参数,如萃取溶剂的类型和体积、分散剂溶剂的类型和体积、萃取时间、pH值和盐效应。在优化条件下,富集因子为185至226,平均回收率为80.45%至95.55%。线性范围为10.0 - 1000.0 μg/L,检测限和定量限分别在0.43 - 1.96 μg/L和1.44 - 6.53 μg/L范围内。相对标准偏差在1.98% - 3.90%范围内(n = 7)。所得结果表明,DLLME结合GC-MS是一种快速简便的测定人尿中MA、PD、KT和TD的方法。