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采用毛细管气相色谱-负化学电离质谱分析法测定人体组织中的有机磷农药残留量。

Determination of organophosphorus pesticide residues in human tissues by capillary gas chromatography-negative chemical ionization mass spectrometry analysis.

作者信息

Russo Mario Vincenzo, Campanella Luigi, Avino Pasquale

机构信息

Facoltà di Agraria (DISTAAM), Università del Molise, Via De Sanctis, 86100 Campobasso, Italy.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2002 Nov 25;780(2):431-41. doi: 10.1016/s1570-0232(02)00629-3.

Abstract

We describe an analytical method that allows the determination of organophosphorus pesticides (OPs) in different human tissues. It involves an extraction procedure with ethanol-ethyl acetate, followed by gel permeation chromatography clean-up step and analysis by capillary gas chromatography-negative chemical ionization mass spectrometry in the selected ion monitoring mode. The method was tested for 37 OPs and the recoveries obtained vary between 60 and 106% with standard deviations ranging between +/-2 and +/-10. These values are independent of the analyzed tissue. Peak area repeatability as RSD for some OPs was < or =4.8% while a good linear relationship in the range 1.0-500 pg microl(-1) with r(2)> or =0.9878 was obtained. The limit of detection for the 37 OPs falls between 0.01 and 0.09 ng g(-1) with an RSD< or =9.5%. The analytical set up in this paper has been used to analyze different samples of human tissues (liver, healthy kidney, cancer kidney and adipose tissue) of 24 patients. The number of the identified OPs in the tissue samples is different (max. 20) according to the sample while their concentration ranges between the limit of detection and 28.0 ng g(-1). The highest concentrations have been determined in liver samples without any pathology (0.4-28.0 ng g(-1)) while the lowest concentrations have been determined in healthy kidney samples (0.01-1.50 ng g(-1)). In the cancer kidney samples OP concentrations vary between 0.03 and 4.6 ng g(-1): these concentrations are more elevated than those determined in healthy kidney samples. The comparison between the concentration of OPs determined in the healthy part, when possible, and those determined in the cancer part of the same kidney sample are very interesting: in fact, in the latter the OP concentration is generally 1-2-times higher than that in the former, an index of lower enzymatic activity in the cancer tissue.

摘要

我们描述了一种可用于测定不同人体组织中有机磷农药(OPs)的分析方法。该方法包括用乙醇 - 乙酸乙酯进行萃取,随后进行凝胶渗透色谱净化步骤,并采用毛细管气相色谱 - 负化学电离质谱在选择离子监测模式下进行分析。该方法针对37种有机磷农药进行了测试,回收率在60%至106%之间,标准偏差在±2至±10之间。这些值与所分析的组织无关。某些有机磷农药的峰面积重复性以相对标准偏差(RSD)计小于或等于4.8%,同时在1.0 - 500 pg μL⁻¹范围内获得了良好的线性关系,相关系数r²大于或等于0.9878。37种有机磷农药的检测限在0.01至0.09 ng g⁻¹之间,相对标准偏差小于或等于9.5%。本文所建立的分析方法已用于分析24例患者的不同人体组织样本(肝脏、健康肾脏、癌肾和脂肪组织)。根据样本不同,组织样本中鉴定出的有机磷农药数量不同(最多20种),其浓度范围在检测限至28.0 ng g⁻¹之间。在无任何病理状况的肝脏样本中测定出最高浓度(0.4 - 28.0 ng g⁻¹),而在健康肾脏样本中测定出最低浓度(0.01 - 1.50 ng g⁻¹)。在癌肾样本中,有机磷农药浓度在0.03至4.6 ng g⁻¹之间:这些浓度高于在健康肾脏样本中测定的浓度。对同一肾脏样本中健康部分(若可能)和癌部分所测定的有机磷农药浓度进行比较非常有趣:实际上,在癌部分有机磷农药浓度通常比健康部分高1 - 2倍,这是癌组织中酶活性较低的一个指标。

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