PMID- 35492944 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220716 IS - 2046-2069 (Electronic) IS - 2046-2069 (Linking) VI - 10 IP - 18 DP - 2020 Mar 11 TI - A simplified fabric phase sorptive extraction method for the determination of amphetamine drugs in water samples using liquid chromatography-mass spectrometry. PG - 10854-10866 LID - 10.1039/c9ra10138a [doi] AB - 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(-1) (MDMA). The correlation coefficients (gamma) were 0.9947 (AM), 0.9925 (MAM), and 0.9918 (MDMA). The detection limits (LOD) were 0.025 ng mL(-1) for AM, 0.029 ng mL(-1) for MAM, and 0.01 ng mL(-1) for MDMA. The corresponding limit of quantification values (LOQ) were 0.083 ng mL(-1), 0.097 ng mL(-1), and 0.031 ng mL(-1), 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. CI - This journal is (c) The Royal Society of Chemistry. FAU - Ruan, Xiaomeng AU - Ruan X AD - Criminal Investigation Police University of China China xinglimei1@sina.com +86 13898164819. FAU - Xing, Limei AU - Xing L AUID- ORCID: 0000-0002-8099-9138 AD - Criminal Investigation Police University of China China xinglimei1@sina.com +86 13898164819. FAU - Peng, Ju AU - Peng J AD - Criminal Investigation Police University of China China xinglimei1@sina.com +86 13898164819. FAU - Li, Shiying AU - Li S AD - Criminal Investigation Police University of China China xinglimei1@sina.com +86 13898164819. FAU - Song, Yiqun AU - Song Y AD - Criminal Investigation Police University of China China xinglimei1@sina.com +86 13898164819. FAU - Sun, Qianqian AU - Sun Q AD - Criminal Investigation Police University of China China xinglimei1@sina.com +86 13898164819. LA - eng PT - Journal Article DEP - 20200317 PL - England TA - RSC Adv JT - RSC advances JID - 101581657 PMC - PMC9050397 COIS- We declare that we do not have any commercial or associative interest that represents a conflict of interest in connection with the work submitted. EDAT- 2020/03/17 00:00 MHDA- 2020/03/17 00:01 PMCR- 2020/03/17 CRDT- 2022/05/02 06:15 PHST- 2019/12/04 00:00 [received] PHST- 2020/02/03 00:00 [accepted] PHST- 2022/05/02 06:15 [entrez] PHST- 2020/03/17 00:00 [pubmed] PHST- 2020/03/17 00:01 [medline] PHST- 2020/03/17 00:00 [pmc-release] AID - c9ra10138a [pii] AID - 10.1039/c9ra10138a [doi] PST - epublish SO - RSC Adv. 2020 Mar 17;10(18):10854-10866. doi: 10.1039/c9ra10138a. eCollection 2020 Mar 11.