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采用顶空固相微萃取和气相色谱 - 电子捕获检测法测定人血清中的有机氯农药和多氯联苯。

Determination of organochlorine pesticides and polychlorinated biphenyls in human serum using headspace solid-phase microextraction and gas chromatography-electron capture detection.

作者信息

López Raul, Goñi Fernando, Etxandia Arsenio, Millán Esmeralda

机构信息

Departamento de Química Aplicada, Universidad del País Vasco, Facultad de Química, Apdo. 1072, 20080-San Sebastián, Spain.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Feb 1;846(1-2):298-305. doi: 10.1016/j.jchromb.2006.09.009. Epub 2006 Oct 11.

Abstract

A simple procedure for the determination of organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) in human serum using headspace solid-phase microextraction (HS-SPME) was developed. The analysis was carried out by gas chromatography (GC) equipped with electron capture detector (ECD). A 2(7-4) Plackett-Burman reduced factorial design for screening and a central composite design for optimizing the significant variables were applied. A 100 microm PDMS fiber, 3/5 headspace ratio (3 ml in 5 ml vial), 85 degrees C extraction temperature, 50 min extraction time, and 1 ml of acidic solution (pH 3) added to 1 ml of diluted serum (1:1) were chosen for the best response in HS extraction mode. The detection limits found were from 1 pg/ml (PCB 167) to 52 pg/ml (beta-HCH), the relative standard deviation for the procedure varied from 3% (PCB 52) to 12% (PCB 189) and the accuracy was checked by using validated solid-phase extraction (SPE) procedure. The method that avoids the use of clean-up steps and the hazardous solvents enabled reliable determinations of the OCPs and the PCBs except beta-HCH. The method was applied to the analysis of 33 human serum samples. The most abundant target compound was p-p'-DDE (range, 0.3-8.0 ng/ml; median value, 2.1 ng/ml). Among the PCBs the prevalent congeners were 138, 153 and 180.

摘要

开发了一种使用顶空固相微萃取(HS-SPME)测定人血清中有机氯农药(OCPs)和多氯联苯(PCBs)的简单方法。分析采用配备电子捕获检测器(ECD)的气相色谱(GC)进行。应用2(7-4) Plackett-Burman简约析因设计进行筛选,并采用中心复合设计优化显著变量。选择100微米的聚二甲基硅氧烷(PDMS)纤维、3/5的顶空比(5毫升小瓶中3毫升)、85℃的萃取温度、50分钟的萃取时间以及向1毫升稀释血清(1:1)中加入1毫升酸性溶液(pH 3),以在HS萃取模式下获得最佳响应。所发现的检测限为1皮克/毫升(PCB 167)至52皮克/毫升(β-六氯环己烷),该方法的相对标准偏差在3%(PCB 52)至12%(PCB 189)之间,并且通过使用经过验证的固相萃取(SPE)程序检查了准确性。该方法避免了使用净化步骤和有害溶剂,能够可靠地测定除β-六氯环己烷之外的OCPs和PCBs。该方法应用于33份人血清样本的分析。含量最高的目标化合物是对,对'-滴滴伊(范围为0.3 - 8.0纳克/毫升;中位数为2.1纳克/毫升)。在多氯联苯中,常见的同系物是138、153和180。

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