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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >AUTOMATED SAMPLE CLEAN-UP AND FRACTIONATION OF CHLORPYRIFOS, CHLORPYRIFOS-METHYL AND METABOLITES IN MUSSELS USING NORMAL-PHASE LIQUID CHROMATOGRAPHY
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AUTOMATED SAMPLE CLEAN-UP AND FRACTIONATION OF CHLORPYRIFOS, CHLORPYRIFOS-METHYL AND METABOLITES IN MUSSELS USING NORMAL-PHASE LIQUID CHROMATOGRAPHY

机译:正相液相色谱法自动纯化和纯化牛乳中的氯霉素,氯氟甲烷和代谢产物

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摘要

An automated method based on normal-phase LC has been developed for the sample clean-up of mussel extracts prior to gas chromatographic analysis of residues of chlorpyrifos, chlorpyrifos-methyl and their metabolites chlorpyrifos-methyl-oxon and 3,5,6-trichloro-2-pyridinol. Pesticides were extracted by means of a high speed blender using acetonitrile-acetone (90:10, v/v). The extract obtained was filtered and concentrated using rotavapor and the residue was dissolved in hexane. One mi of the hexanoic extract was injected on the silica-gel column, using hexane as mobile phase. Pesticides and metabolites were eluted in fat-free fractions with different mixtures of hexane-ethyl acetate. Diode array detection allowed monitoring on-line the elution of lipids. Purified extracts were analyzed by GC using nitrogen-phosphorus detection for quantitation and MS for confirmatory purposes, The method is fully automated from the injection of the extract to the collection of fractions, which are directly injected into the GC system. In this way, neither further clean-up nor solvent exchange were necessary prior to GC analysis. Recoveries obtained from fortified mussel samples at two concentration levels -100 and 20 ng g(-1) for parent pesticides and 200 and 40 ng g(-1) for metabolites- were higher than 90%. Limits of detection of the whole procedure of analysis were lower than 1 ng g(-1) for parent pesticides and than 10 ng g(-1) for metabolites, This method has been successfully applied to bioconcentration studies with mussels exposed to chlorpyrifos. Chlorpyrifos and its metabolic derivative 3,5,6-trichloro-2-pyridinol were detected and confirmed by MS in analyzed samples. (C) 1997 Elsevier Science B.V
机译:已开发出一种基于正相液相色谱的自动化方法,用于在对毒死rif,毒死rif甲基及其代谢产物毒死rif,甲基氧还和3,5,6-三氯残留物进行气相色谱分析之前,对贻贝提取物进行样品净化。 -2-吡啶醇。使用乙腈-丙酮(90:10,v / v)通过高速搅拌机提取农药。过滤获得的萃取液,并使用旋转蒸发仪浓缩,并将残余物溶于己烷中。使用己烷作为流动相,将一毫升的己酸萃取液注入硅胶柱。农药和代谢物用不同的己烷-乙酸乙酯混合物洗脱,得到无脂馏分。二极管阵列检测允许在线监测脂质的洗脱。纯化的提取物通过使用氮磷检测的GC进行定量分析,并通过MS进行确认,该方法是全自动的,从注入提取物到馏分收集,将其直接注入GC系统。这样,在GC分析之前,无需进一步清理或更换溶剂。从强化贻贝样品中两个浓度水平(母体农药为100和20 ng g(-1),代谢产物为200和40 ng g(-1))获得的回收率均高于90%。对于母体农药,整个分析过程的检出限均低于1 ng g(-1),对于代谢产物,其检出限低于10 ng g(-1)。该方法已成功地应用于贻贝暴露于毒死rif的生物浓缩研究中。质谱检测并测定了毒死rif及其代谢衍生物3,5,6-三氯-2-吡啶醇。 (C)1997年Elsevier Science B.V

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