首页> 外文期刊>Analytical methods >Ammonium salting out extraction with analyte preconcentration for sub-part per billion quantitative analysis in surface, ground and drinking water by flow injection tandem mass spectrometry
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Ammonium salting out extraction with analyte preconcentration for sub-part per billion quantitative analysis in surface, ground and drinking water by flow injection tandem mass spectrometry

机译:流动注射串联质谱法对铵盐析出进行分析物预富集萃取,用于地表,地下水和饮用水中十亿分之一的定量分析

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A recently-reported extraction method that merged principles of QuEChERS and salting out liquida€“liquid extraction (SALLE) by using ammonium salts (chloride, acetate, formate) has been improved for high-throughput quantitation of bioactive chemicals in water by flow injection tandem mass spectrometry (FI/MS/MS). The new method for water analysis uses the ratio of acetonitrile/water adjusted to yield extract preconcentration in one step: 7.0 mL water aliquot, 3.5 mL of acetonitrile extraction solvent and 3.0 g of NH4Cl (s) resulted in post-extraction acetonitrile phase volume of 1.4 mL (extract preconcentration factor = 5). This preconcentration factor can be adjusted by changing the acetonitrile/water aliquot ratio to achieve the desired sensitivity while optimizing method performance. The acetonitrile/water partition coefficients (Kaw) of analytes in the acetonitrile/water/NH4Cl ternary systems were measured during method development. Kaw values were used to predict analyte recoveries when the acetonitrile/water ratios were varied in the extraction procedure. The effect of aqueous system pH was evaluated and the results were used for extraction optimization. A validation study was successfully conducted in creek, pond, ground, and drinking water for the following pesticides: aminocyclopyrachlor methyl, azimsulfuron, chlorantraniliprole, chlorimuron ethyl, chlorsulfuron, cyantraniliprole, diuron, flupyrsulfuron methyl, hexazinone, oxamyl, methomyl, sulfometuron methyl, triflusulfuron methyl. The method met the stringent 0.1 ??g La?’1 (ppb) limit of quantitation (LOQ) specified by the European Union for 10 out of 13 pesticides tested. The LOQ for the 3 least responsive analytes, i.e. chlorsulfuron, oxamyl and methomyl, was 0.3 ??g La?’1. Limits of detection (LODs) were between 10 and 100 ng La?’1 (ppt). FI/MS/MS acquisition time was 30 seconds/injection. The correlation between analyte recoveries and publicly-available physicochemical properties, such as octanol/water partition coefficients (Kow) and aqueous solubility, was also assessed, allowing the prediction of method applicability to other chemicals, such as pharmaceuticals and other pesticides not tested in the study.
机译:最近报道了一种提取方法,该方法结合了QuEChERS的原理和通过使用铵盐(氯化物,乙酸盐,甲酸盐)盐析液体提取液(SALLE)的方法,从而可以通过流动注射串联法高通量定量水中的生物活性化学品。质谱(FI / MS / MS)。进行水分析的新方法可将乙腈/水的比例调整为可一步完成萃取物预浓缩:7.0 mL等分试样,3.5 mL乙腈萃取溶剂和3.0 g NH4Cl导致萃取后乙腈相体积的增加。 1.4 mL(提取物预浓缩因子= 5)。可以通过更改乙腈/水等分试样的比例来调整该预浓缩系数,以实现所需的灵敏度,同时优化方法性能。在方法开发过程中,对乙腈/水/ NH4Cl三元系统中分析物的乙腈/水分配系数(Kaw)进行了测量。当乙腈/水的比例在提取过程中发生变化时,使用Kaw值预测分析物的回收率。评估了水性系统pH的影响,并将结果用于提取优化。已在小河,池塘,地下水和饮用水中成功进行了以下农药的验证研究:氨基环吡氯甲基,阿齐磺隆,氯吡咯胺,氯嘧磺隆,氯磺隆,氰基氰基丙烯腈,二嘧磺隆,氟嘧磺隆甲基,六嗪酮,氧戊基,甲磺酰基,三氟磺隆,磺胺甲磺隆甲基。该方法满足了欧盟规定的13种农药中的10种的0.1 µg La?1(ppb)严格的定量限(LOQ)。三种反应最慢的分析物,即氯磺隆,草酰胺和甲磺胺的最低定量限为0.3 ?? g La?-1。检出限(LOD)在10至100 ng La?’1(ppt)之间。 FI / MS / MS采集时间为30秒/进样。还评估了分析物回收率与公众可利用的理化特性(例如辛醇/水分配系数(Kow)和水溶性)之间的相关性,从而预测了该方法对其他化学品的适用性,例如药物和其他未在农药中测试的农药。研究。

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