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采用气相色谱-串联质谱法测定土壤中有机氯农药的简单提取和净化程序的开发。

Development of a simple extraction and clean-up procedure for determination of organochlorine pesticides in soil using gas chromatography-tandem mass spectrometry.

机构信息

Department of Plant Sciences, Quaid-i-Azam University, Islamabad, Pakistan.

出版信息

J Chromatogr A. 2010 Apr 23;1217(17):2933-9. doi: 10.1016/j.chroma.2010.02.060. Epub 2010 Mar 3.

Abstract

A procedure based on QuEChERS extraction and a simultaneous liquid-liquid partition clean-up was developed. The procedure involved extraction of hydrated soil samples using acetonitrile and clean-up by liquid-liquid partition into n-hexane. The hexane extracts produced were clean and suitable for determination using gas chromatography-tandem mass spectrometry (GC-MS/MS). The method was validated by analysis of soil samples, spiked at five levels between 1 and 200 microg kg(-1). The recovery values were generally between 70 and 100% and the relative standard deviation values (%RSDs) were at or below 20%. The procedure was validated for determination of 19 organochlorine (OC) pesticides. These were hexachlorobenzene (HCB), alpha-HCH, beta-HCH, gamma-HCH, heptachlor, heptachlor epoxide (trans), aldrin, dieldrin, chlordane (trans), chlordane (cis), oxychlordane, alpha-endosulfan, beta-endosulfan, endosulfan sulfate, endrin, p,p'-DDT, o,p'-DDT, p,p'-DDD and p,p'-DDE. The method achieved low limits of detection (LOD; typically 0.3 microg kg(-1)) and low limits of quantification (LOQ; typically 1.0 microg kg(-1)). The method performance was also assessed using five fortified soil samples with different physico-chemical properties and the method performance was consistent for the different types of soil samples. The proposed method was compared with an established procedure based on Soxtec extraction. This comparison was carried out using six soil samples collected from regions of Pakistan with a history of intensive pesticide use. The results of this comparison showed that the two procedures produced results with good agreement. The proposed method produced cleaner extracts and therefore led to lower limits of quantification. The proposed method was less time consuming and safer to use. The six samples tested during this comparison showed that soils from cotton growing regions contained a number of persistent OC residues at relatively low levels (<10 microg kg(-1)). These residues were alpha-HCH, gamma-HCH, heptachlor, chlordane (trans), p,p'-DDT, o,p'-DDT, p,p'-DDD, p,p'-DDE, beta-endosulfan and endosulfan sulfate.

摘要

建立了一种基于 QuEChERS 提取和同时液-液分配净化的方法。该方法涉及使用乙腈提取水合土壤样品,并通过液-液分配到正己烷中进行净化。所得的正己烷提取物干净,适合使用气相色谱-串联质谱(GC-MS/MS)进行测定。该方法通过在 1 至 200μgkg(-1) 五个水平对土壤样品进行加标分析进行了验证。回收率一般在 70%至 100%之间,相对标准偏差(%RSD)在 20%或以下。该程序经过验证可用于测定 19 种有机氯(OC)农药。这些农药包括六氯苯(HCB)、α-六氯环己烷、β-六氯环己烷、γ-六氯环己烷、七氯、七氯环氧(反式)、艾氏剂、狄氏剂、氯丹(反式)、氯丹(顺式)、氧氯丹、α-硫丹、β-硫丹、硫丹硫酸盐、异狄氏剂、p,p'-滴滴涕、o,p'-滴滴涕、p,p'-滴滴滴和 p,p'-滴滴伊。该方法实现了低检测限(LOD;通常为 0.3μgkg(-1))和低定量限(LOQ;通常为 1.0μgkg(-1))。还使用具有不同物理化学性质的五种加标土壤样品评估了方法的性能,并且该方法在不同类型的土壤样品中的性能是一致的。将所提出的方法与基于 Soxtec 提取的既定方法进行了比较。使用从巴基斯坦历史上大量使用农药的地区收集的六份土壤样品进行了这一比较。该比较的结果表明,这两种方法的结果具有良好的一致性。所提出的方法产生的提取物更干净,因此定量限更低。该方法耗时更少,使用更安全。在这次比较中测试的六个样品表明,来自棉花种植区的土壤含有一些持久性 OC 残留,水平相对较低(<10μgkg(-1))。这些残留物包括α-六氯环己烷、γ-六氯环己烷、七氯、氯丹(反式)、p,p'-滴滴涕、o,p'-滴滴涕、p,p'-滴滴滴、p,p'-滴滴伊、β-硫丹和硫丹硫酸盐。

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