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A simplified fabric phase sorptive extraction method for the determination of amphetamine drugs in water samples using liquid chromatography-mass spectrometry

机译:使用液相色谱 - 质谱法测定水样中含水样品中的Amphetamine药物的简化织物相吸附方法

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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 ( γ ) 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.
机译:织物相吸附萃取(FPSE)可以直接提取靶分析物并同时确定来自复杂样品矩阵的许多类似物质。此外,它具有非常高的化学稳定性。因此,我们使用织物相吸附萃取分析水中三种amphetamine药物(Amphetamine(Am),甲基苯丙胺(MAM)和3,4-甲基二氧基戊酰胺(MDMA))。这与超高效液相色谱和串联质谱相连。研究了不同吸附剂化学的影响,如吸附时间,反萃取溶剂比率,背提取时间和盐效应对提取效率的研究;确定最佳操作条件。使用短链聚(四氢呋喃)(PTHF)产生中极性极性涂覆的FPSE培养基。这是兴趣分析的最有效的提取介质。在优化的条件下,三种amphetamine药物的线性范围为0.1-150.0(AM,MAM)和0.5-200ng mL〜(α1)(MDMA)。相关系数(γ)为0.9947(AM),0.9925(MAM)和0.9918(MDMA)。对于MAM的0.029ng ml〜(α1),检测限值(LOD)为0.025 ng(α1),MDMA为0.029ng ml〜(α1)和0.01 ng ml〜(α1)。定量值(LOQ)的相应限制为0.083ng ml〜(α1),0.097ng ml〜(α1),0.031ng ml〜(α1)。回收率分别为73.4-91.6%,82.6-95.4%和92.7-95.3%,相对标准偏差(RSD)分别为1.65-6.88%,1.38-6.11%和1.58-7.34%。此外,我们的方法可以成功地应用于废水样品中的安非胺分析,同时为未来检测此类物质的基础。

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