Ruan Xiaomeng, Xing Limei, Peng Ju, Li Shiying, Song Yiqun, Sun Qianqian
Criminal Investigation Police University of China China
RSC Adv. 2020 Mar 17;10(18):10854-10866. doi: 10.1039/c9ra10138a. eCollection 2020 Mar 11.
Fabric phase sorptive extraction (FPSE) can directly extract the target analytes and simultaneously determine many similar substances from complicated sample matrices. Also, it has very high chemical stability. Therefore, we used fabric phase sorptive extraction to analyze three amphetamine drugs (amphetamine (AM), methamphetamine (MAM), and 3,4-methylenedioxymethamphetamine (MDMA)) in water. This was coupled with ultrahigh-performance liquid chromatography and tandem mass spectrometry. The effects of different sorbent chemistries such as sorption time, ratios of back-extraction solvents, back-extraction time, and the salt effect on the extraction efficiency were studied; the optimum operation conditions were determined. Medium polarity polar polymer-coated FPSE media were created using short-chain poly (tetrahydrofuran) (PTHF). This is the most efficient extraction media for the analytes of interest. Under the optimized conditions, the linear range of the three amphetamine drugs were 0.1-150.0 (AM, MAM) and 0.5-200 ng mL (MDMA). The correlation coefficients () were 0.9947 (AM), 0.9925 (MAM), and 0.9918 (MDMA). The detection limits (LOD) were 0.025 ng mL for AM, 0.029 ng mL for MAM, and 0.01 ng mL for MDMA. The corresponding limit of quantification values (LOQ) were 0.083 ng mL, 0.097 ng mL, and 0.031 ng mL, respectively. The recoveries were 73.4-91.6%, 82.6-95.4%, and 92.7-95.3%, respectively, and the relative standard deviations (RSD) were 1.65-6.88%, 1.38-6.11%, and 1.58-7.34%, respectively. Moreover, our method can be successfully applied for the analysis of amphetamines in wastewater samples, and at the same time, lays the foundation for the future detection of such substances.
织物相吸附萃取(FPSE)能够直接萃取目标分析物,同时可从复杂的样品基质中同时测定多种类似物质。此外,它具有很高的化学稳定性。因此,我们采用织物相吸附萃取法对水中的三种苯丙胺类药物(苯丙胺(AM)、甲基苯丙胺(MAM)和3,4-亚甲基二氧基甲基苯丙胺(MDMA))进行分析。该方法与超高效液相色谱和串联质谱联用。研究了不同吸附剂化学性质如吸附时间、反萃取溶剂比例、反萃取时间以及盐效应等对萃取效率的影响;确定了最佳操作条件。使用短链聚(四氢呋喃)(PTHF)制备了中等极性的极性聚合物涂层FPSE介质。这是用于目标分析物的最有效萃取介质。在优化条件下,三种苯丙胺类药物的线性范围分别为0.1 - 150.0(AM、MAM)和0.5 - 200 ng/mL(MDMA)。相关系数()分别为0.9947(AM)、0.9925(MAM)和0.9918(MDMA)。检测限(LOD)分别为AM 0.025 ng/mL、MAM 0.