首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Enantio selective determination of the organochlorine pesticide bromocyclen in spiked fish tissue using solid-phase microextraction coupled to gas chromatography with ECD and ICP-MS detection
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Enantio selective determination of the organochlorine pesticide bromocyclen in spiked fish tissue using solid-phase microextraction coupled to gas chromatography with ECD and ICP-MS detection

机译:固相微萃取-气相色谱-ECD和ICP-MS检测对虾鱼组织中有机氯农药溴环素的对映体选择性测定

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A method for enantioselective determination of bromocyclen enantiomers in fish tissue has been developed. The enantiomers were resolved by capillary gas chromatography (GC) using a commercial chiral column (CP-Chirasil-Dex CB) and a temperature program from 50 degrees C (held for 1 min), raised to 140 degrees C at 40 degrees C min(-1) and then raised at 0.2 degrees C min(-1) to 155 degrees C. This enantioselective gas chromatographic separation was combined with a clean-up/enrichment procedure based on solid-phase microextraction (SPME). Under SPME optimized conditions, precision, linearity range and detection limits of the developed SPME-enantioselective GC procedure were evaluated and compared using two different detection systems: a classical electron-capture detection (ECD) and an element specific detection using inductively coupled plasma mass spectrometry (ICP-MS). The SPME-GC-ECD method exhibited an excellent sensitivity, with detection limits of 0.2 ng L-1 for each enantionner of bromocyclen. Although ICP-MS offered poorer detection limits (7 ng L-1 as Br, equivalent to 36 ng L-1 of each enantiomer) than conventional ECD detector, it proved to be clearly superior in terms of selectivity. The relative potential and performance of the two compared methods for real-life analysis has been illustrated by the determination of enantiomers of bromocyclen in spiked tissue extracts of trout. (c) 2007 Elsevier B.V. All rights reserved.
机译:已经开发了一种对鱼组织中溴环十二烷对映体进行对映选择性测定的方法。对映异构体通过毛细管气相色谱法(GC)使用市售手性色谱柱(CP-Chirasil-Dex CB)和温度程序从50摄氏度(保持1分钟)拆分,在40摄氏度(分钟)升至140摄氏度( -1),然后在0.2°C min(-1)升至155°C。此对映选择性气相色谱分离与基于固相微萃取(SPME)的净化/富集程序结合在一起。在SPME优化的条件下,使用两种不同的检测系统评估并比较了已开发的SPME对映选择性GC程序的精密度,线性范围和检测极限:经典电子捕获检测(ECD)和使用电感耦合等离子体质谱的元素特异性检测(ICP-MS)。 SPME-GC-ECD方法显示出极好的灵敏度,每个溴环十二烷对映体的检出限为0.2 ng L-1。尽管ICP-MS的检测限(常规浓度为7 ng L-1,相当于Br的每种对映体为36 ng L-1)较常规ECD检测器差,但在选择性方面却被证明是优越的。通过对鳟鱼加标组织提取物中溴环素的对映异构体的测定,可以说明两种比较方法在现实生活中的相对潜力和性能。 (c)2007 Elsevier B.V.保留所有权利。

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