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采用气相色谱-串联质谱法测定农业人群血浆样本中呋喃丹、西维因及其主要代谢物。

Determination of carbofuran, carbaryl and their main metabolites in plasma samples of agricultural populations using gas chromatography-tandem mass spectrometry.

作者信息

Petropoulou Syrago-Styliani E, Tsarbopoulos Anthony, Siskos Panayotis A

机构信息

Bioanalytical Laboratory, GAIA Research Center, The Goulandris Natural History Museum, 100 Othonos str., 145 62, Kifissia, Greece.

出版信息

Anal Bioanal Chem. 2006 Aug;385(8):1444-56. doi: 10.1007/s00216-006-0569-0. Epub 2006 Jul 25.

Abstract

A gas chromatography-tandem mass spectrometric (GC-MS/MS) method has been developed for the determination of carbofuran (2,3-dihydro-2,2-dimethylbenzofuran-7-yl methylcarbamate), carbaryl (1-naphthyl-N-methylcarbamate) and their main metabolites in human blood plasma. Optimization of the isolation of the compounds from plasma matrix included the precipitation, denaturation and digestion of plasma proteins. Derivatization was achieved by the use of trifluoroacetic acid anhydride and was optimized for temperature, time and volume of derivatization agent. In the proposed method, a mild precipitation technique was applied using beta-mercaptoethanol and ascorbic acid in combination with solid-phase extraction technique using Oasis HLB (Hydrophobic Lipophilic Balance) cartridges for further clean up of samples. Carbamate linkage was not hydrolyzed to its phenol product, but both carbamate phenol and ketones were transformed into trifluoroacetyl derivatives in order to become volatile compounds and were determined using tandem mass spectrometry. The linearity of the method was shown for nine concentrations in the range of 0.50-250 ng mL(-1) in fortified plasma aliquots. Limits of detection (LODs) for all compounds ranged from 0.015-0.151 ng mL(-1). Inter-day and intra-day assays (RSD) for all compounds, at three concentration levels of 2.5, 25 and 100 ng mL(-1) (n=3) in fortified plasma samples were less than 18%. Accuracy (%E (r)) was calculated at three concentration levels, 8, 80 and 160 ng mL(-1) (n=3), and ranged from -12.0 to 15.0%. Matrix effect was evaluated so mean recoveries were calculated for all compounds and ranged from 81-107%. Specificity for the use of this method to biological monitoring studies was achieved including four main metabolites of CF, 1-naphthol and 2-naphthol from the naphthalene metabolism pathways, and both the parent compound of carbofuran and carbaryl. The proposed method was applied to plasma samples of pesticide users.

摘要

已开发出一种气相色谱 - 串联质谱(GC-MS/MS)方法,用于测定人血浆中的克百威(2,3 - 二氢 - 2,2 - 二甲基苯并呋喃 - 7 - 基甲基氨基甲酸酯)、西维因(1 - 萘基 - N - 甲基氨基甲酸酯)及其主要代谢物。从血浆基质中分离化合物的优化过程包括血浆蛋白的沉淀、变性和消化。通过使用三氟乙酸酐进行衍生化,并对衍生化试剂的温度、时间和体积进行了优化。在所提出的方法中,采用β - 巯基乙醇和抗坏血酸进行温和沉淀技术,并结合使用Oasis HLB(疏水亲脂平衡)柱的固相萃取技术对样品进行进一步净化。氨基甲酸酯键未水解为其酚类产物,但氨基甲酸酯酚和酮类均转化为三氟乙酰衍生物,以便成为挥发性化合物,并使用串联质谱法进行测定。在加标血浆等分试样中,该方法在0.50 - 250 ng mL⁻¹范围内的九个浓度下表现出线性。所有化合物的检测限(LOD)范围为0.015 - 0.151 ng mL⁻¹。在加标血浆样品中,三种浓度水平(2.5、25和100 ng mL⁻¹,n = 3)下所有化合物的日间和日内测定(RSD)均小于18%。在三个浓度水平(8、80和160 ng mL⁻¹,n = 3)下计算准确度(%E(r)),范围为 - 12.0至15.0%。评估了基质效应,因此计算了所有化合物的平均回收率,范围为81 - 107%。该方法用于生物监测研究的特异性得以实现,包括克百威的四种主要代谢物、萘代谢途径中的1 - 萘酚和2 - 萘酚,以及克百威和西维因的母体化合物。所提出的方法应用于农药使用者的血浆样品。

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