Department of Toxicology, Medical University of Gdańsk, Al. Gen. Hallera 107, 80-416 Gdańsk, Poland.
Talanta. 2018 Jan 1;176:165-171. doi: 10.1016/j.talanta.2017.08.011. Epub 2017 Aug 9.
A 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 in n-hexane (on-line derivatization). The optimized method was validated, with linearity established from 0.05 to 25ngmL and R values > 0.99. Obtained quantification limits were in the range of 0.06-0.08ngmL, 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.
建立了一种新型、快速、环保的分析方法,采用填充固相微萃取(MEPS)与大体积进样-气相色谱-质谱联用(MEPS-LVI-GC-MS),用于测定人尿中 5 种拟除虫菊酯代谢物(顺式-2,2-二甲基-3-(2-氯-3,3,3-三氟-1-丙烯基)-环丙烷羧酸、顺式/反式-3-(2,2-二氯乙烯基)-2,2-二甲基环丙烷-1-羧酸、顺式-(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)。MEPS 采用手动半自动注射器(eVol)在线进行,优化了多个参数,包括样品 pH 值、萃取吸附剂、洗涤溶剂、洗脱溶剂体积和类型以及抽提-洗脱循环次数。用 C18 固相从酶解尿中提取分析物,随后用 1,1,1,3,3,3-六氟异丙醇和二异丙基碳二亚胺在正己烷中的混合物进行在线衍生和洗脱(在线衍生)。对优化方法进行了验证,线性范围为 0.05-25ngmL,相关系数(R)大于 0.99。获得的定量限范围为 0.06-0.08ngmL,所有分析物的精密度(相对标准偏差,RSD)均低于 14%。通过分析 21 个尿液样本,用基于液液萃取-气相色谱-质谱(LLE-GC-MS)的参考方法对该方法进行了交叉验证。