Microextraction technique associated with gas chromatography–mass spectrometry for determining pesticide residues in urine

色谱法 检出限 化学 气相色谱-质谱法 质谱法 气相色谱法 分析物
作者
Thaís L. R. Silva,José Humberto de Queiróz,André Fernando de Oliveira,Alessandra Aparecida Zinato Rodrigues,Antônio Augusto Neves,Patrícia Aparecida Fontes Vieira,José Humberto de Queiróz,Verônica O. de P. Barbosa
出处
期刊:Journal of Environmental Science and Health Part B-pesticides Food Contaminants and Agricultural Wastes [Taylor & Francis]
卷期号:57 (3): 165-175 被引量:8
标识
DOI:10.1080/03601234.2022.2038505
摘要

Urine is one of the biological matrices most used for detecting human contamination, as it is representative and easily obtained via noninvasive sampling. This study proposes a fast, accurate, and ecological method based on liquid-liquid microextraction with low-temperature partition (μLLE/LTP). It was validated to determine nine pesticides (lindane, alachlor, aldrin, chlorpyrifos, dieldrin, endrin, DDT, bifenthrin, and permethrin) in human urine, in association with gas chromatography coupled with mass spectrometry (GC-MS). The technique was optimized through a factorial design. The best conditions for the simultaneous extraction of the analytes comprised the addition of 600 µL of water and 600 µL of acetonitrile (extracting solvent) to a 500-µL urine sample, followed by vortexing for 60 s. By freezing the samples for 4 h, it was possible to extract the pesticides and perform the extract clean-up simultaneously. The parameters selectivity, linearity, limit of detection (LOD), limit of quantification (LOQ), precision, and accuracy were used to appraise the performance of the method. Good values of selectivity and linearity (R2 > 0.990), LOQ (0.39-1.02 μg L-1), accuracy (88-119% recovery), and precision (%CV ≤ 15%) were obtained. The μLLE/LTP-GC-MS method was applied to authentic urine samples collected from volunteers in Southeast Brazil.

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