Abstract Off-line microextraction by packed sorbent combined with on solid support derivatization and GC-MS: Application for the analysis of five pyrethroid metabolites in urine samples
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Off-line microextraction by packed sorbent combined with on solid support derivatization and GC-MS: Application for the analysis of five pyrethroid metabolites in urine samples

机译:用填充的吸附剂与固体载体衍生化和GC-MS相结合的离线微萃取:用于分析尿液样本中五种拟除虫菊酯代谢物的应用

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AbstractA novel, fast and eco-friendly analytical method using microextraction by packed sorbent coupled to large volume injection-gas chromatography-mass spectrometry (MEPS-LVI-GC-MS) was developed for the determination of five pyrethroid metabolites (cis-2,2-dimethyl-3-(2-chloro-3,3,3-trifluoro-1-propenyl)-cyclopropanecarboxylic acid,cis/trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylic acids,cis-(2,2-dibromovinyl)-2,2-dimethylcyclopropane-1-carboxylic acid and 3-phenoxybenzoic acid) in human urine. MEPS was performed off-line using a manually-operated semiautomatic syringe (eVol), and several parameters including the sample pH, extraction sorbent, washing solvent, volume and type of elution solvent and number of draw-eject cycles were optimized. Analytes were extracted from enzymatically hydrolyzed urine using a C18 solid phase with subsequent simultaneous derivatization and elution with a mixture of 1,1,1,3,3,3-hexafluoroisopropanol and diisopropylcarbodiimide inn-hexane (on-linederivatization). The optimized method was validated, with linearity established from 0.05 to 25ngmL?1and R values > 0.99. Obtained quantification limits were in the range of 0.06–0.08ngmL?1, and the precision expressed as relative standard deviation (RSD) was below 14% for all of the analytes. The method was cross-validated with a reference approach based on liquid-liquid extraction-gas chromatography-mass spectrometry (LLE-GC-MS) by analyzing 21 urine samples.
机译:<![cdata [ 抽象 使用填充吸附剂的微萃取到大容量注射气相色谱 - 质谱法(MEPS-LVI)使用微萃取的新颖,快速和生态友好的分析方法(MEPS-LVI开发了-GC-MS)用于测定五种拟除虫菊酯代谢物( CIS -2,2-二甲基-3-(2-氯-3,3,3-三氟-1 - 丙酮烯基) - 环丙烷羧酸, CIS / 转晶>斜斜体> -3-(2,2-二氯丙烯基)-2,2-二甲基环丙烷-1 - 羧酸, CIS - (2,2-二溴乙烯基)-2,2-二甲基环丙烷-1-羧酸和3-苯氧基苯甲酸)在人尿中。使用手动操作的半自动注射器(EVOL)离线进行MEP,并优化了几种包括样品pH,提取吸附剂,洗涤溶剂,体积和洗脱溶剂的体积和类型的参数。使用C18固相从酶促水解尿液中提取分析物,随后的同时衍生化和用1,1,1,3,3,3-六氟异丙醇和二异丙基碳二亚胺的混合物在 n - 横向(在线衍生化)。验证了优化的方法,用线性建立从0.05到25×10ngml ?1 和r值> 0.99。获得的量化限制在0.06-0.08ngml Δ1,并且作为相对标准偏差(RSD)表示的精度低于14%分析物。通过分析21例尿液样品,通过基于液 - 萃取 - 气相色谱 - 质谱(LLE-GC-MS)的参考方法交叉验证。

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