Abstract An efficient analytical method for determination of <ce:italic>S</ce:italic>-phenylmercapturic acid in urine by HPLC fluorimetric detector to assessing benzene exposure
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An efficient analytical method for determination of S-phenylmercapturic acid in urine by HPLC fluorimetric detector to assessing benzene exposure

机译:HPLC荧光探测器测定 s - 苯基MmerciC酸的高效分析方法,通过HPLC荧光探测器评估苯暴露

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Abstract 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. ]]>
机译:<![cdata [ 抽象 苯是一个重要的职业和环境污染,天然存在于石油和钢铁工业中的副产品。毒理学研究显示出明显的乳腺毒性作用,导致白血病和其他血细胞紊乱。评估苯暴露是通过生物标志物作为反式,反式 - 墨西哥酸( attm )和 s - 苯基雌酸( s -pma)。由于 s -pma的特异性,已经提出了这种生物标志物在空气中抑制较低的苯。本研究的目的是通过高性能液相色谱法验证定量 S -PMA的分析方法,用荧光检测器进行高效液相色谱法。使用C-18相,通过固相萃取(SPE)进行 S -pma的分析方法的发展。在75 ℃和氮气中,将被提取至水浴,并与分析物浓度,然后用碱性水解和用甘氨酸衍生化。色谱条件是反相C-18柱(240 mm,4 mm和5 μm)在35 °C;乙腈和0.5%乙酸(50:50)作为流动相,流动为0.8 ml / min。检测和定量极限分别为0.22 μg/ l,分别为0.68 μg/ l。通过简单的线性回归验证线性度,该方法在10-100 μg/ L的范围内呈现出良好的线性度。对于 s -pma使用40,60,80和100 μg/ l的斜体效应。介入和间隔的精度显示出少于10%的变异系数,恢复的速度为83.4至102.8%,平均为94.4%。 s -pma储存在尿液中的稳定性,尿液中尿液:Hsp sp =“0.25”/>°C为七周。结论是,这种方法呈现出令人满意的优点结果。这种确定尿的方法 s -pma显示出足够的敏感性,用于使用 s -pma作为生物标志物的敌人和环境暴露对苯曝光。 ]]>

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