Mendes Michele P Rocha, Silveira Josianne Nicácio, Andre Leiliane Coelho
Department of Clinical and Toxicological Analysis, Faculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Department of Clinical and Toxicological Analysis, Faculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, Brazil.
J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Sep 15;1063:136-140. doi: 10.1016/j.jchromb.2017.07.039. Epub 2017 Aug 18.
Benzene is an important occupational and environmental contaminant, naturally present in petroleum and as by-product in the steel industry. Toxicological studies showed pronounced myelotoxic action, causing leukemic and others blood cells disorders. Assessing of benzene exposure is performed by biomarkers as trans, trans-muconic acid (AttM) and S-phenylmercapturic acid (S-PMA) in urine. Due to specificity of S-PMA, this biomarker has been proposed to asses lower levels of benzene in air. The aim of this study was to validate an analytical method for the quantification of S-PMA by High-Performance Liquid Chromatography with fluorometric detector. The development of an analytical method of S-PMA in urine was carried out by solid phase extraction (SPE) using C-18 phase. The eluated were submitted to water bath at 75°C and nitrogen to analyte concentration, followed by alkaline hydrolysis and derivatization with monobromobimane. The chromatography conditions were reverse phase C-18 column (240mm, 4mm and 5μm) at 35°C; acetonitrile and 0.5% acetic acid (50:50) as mobile phase with a flow of 0.8mL/min. The limits of detection and quantification were 0.22μg/L and 0.68μg/L, respectively. The linearity was verified by simple linear regression, and the method exhibited good linearity in the range of 10-100μg/L. There was no matrix effect for S-PMA using concentrations of 40, 60, 80 and 100μg/L. The intra- and interassay precision showed coefficient of variation of less than 10% and the recovery ranged from 83.4 to 102.8% with an average of 94.4%. The stability of S-PMA in urine stored at -20°C was of seven weeks. The conclusion is that this method presents satisfactory results per their figures of merit. This proposed method for determining urinary S-PMA showed adequate sensitivity for assessment of occupational and environmental exposure to benzene using S-PMA as biomarker of exposure.
苯是一种重要的职业和环境污染物,天然存在于石油中,也是钢铁行业的副产品。毒理学研究表明,苯具有明显的骨髓毒性作用,可导致白血病和其他血细胞紊乱。通过尿液中的反式,反式粘康酸(AttM)和S-苯基巯基尿酸(S-PMA)等生物标志物来评估苯暴露情况。由于S-PMA的特异性,已提出将该生物标志物用于评估空气中较低水平的苯。本研究的目的是验证一种使用荧光检测器的高效液相色谱法定量S-PMA的分析方法。采用C-18固相萃取(SPE)法开展尿液中S-PMA分析方法的研究。洗脱液在75°C水浴中加热并用氮气浓缩至分析物浓度,然后进行碱性水解并用单溴联苯胺衍生化。色谱条件为:在35°C下使用反相C-18柱(240mm,4mm和5μm);以乙腈和0.5%乙酸(50:50)作为流动相,流速为0.8mL/min。检测限和定量限分别为0.22μg/L和0.68μg/L。通过简单线性回归验证线性,该方法在10-100μg/L范围内表现出良好的线性。使用40、60、80和100μg/L的浓度时,S-PMA不存在基质效应。批内和批间精密度的变异系数均小于10%,回收率在83.4%至102.8%之间,平均为94.4%。S-PMA在-20°C储存的尿液中的稳定性为七周。结论是,该方法的各项性能指标均呈现出令人满意的结果。所提出的测定尿中S-PMA的方法,以S-PMA作为暴露生物标志物,对评估职业和环境苯暴露具有足够的灵敏度。