Laboratory of Clinical, Forensic and Environmental Toxicology, University of Liege (ULg), CHU (B35), 4000 Liege, Belgium; Center for Interdisciplinary Research on Medicines (C.I.R.M.), University of Liege (ULg), CHU (B35), 4000 Liege, Belgium.
J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Feb 15;949-950:37-47. doi: 10.1016/j.jchromb.2014.01.002. Epub 2014 Jan 8.
Phthalates, parabens and 2-hydroxy-4-methoxybenzophenone or benzophone-3 are thought to act as endocrine disrupting chemicals, being able to disrupt the endocrine balance and therefore able to lead to some hormonal diseases. Numerous large-scale biomonitoring studies have detected the biomarkers of these compounds in more than 75% of the general population. To assess the exposure to these chemicals, we developed an analytical method based on a Solid Phase Extraction (SPE) prior to ultra high pressure liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) for the simultaneous measurement of seven phthalate metabolites (monobenzyl phthalate, mono-n-butyl phthalate, mono-iso-butyl phthalate, mono-2-ethylhexyl phthalate, mono-2-ethyl-5-hydroxyhexyl phthalate, mono-2-ethyl-5-oxohexyl phthalate, monoethyl phthalate), four parabens (methyl paraben, ethyl paraben, n-propyl paraben, n-butyl parabens) and benzophenone-3 in human urine. The distinction between unconjugated, glucuro- and sulfoconjugated forms was achieved using different enzymatic hydrolyses. The whole procedure was validated according to the total error approach, and was demonstrated to be linear (regression coefficient ranging from 0.987 to 0.998) and accurate (inter and intra assay precision <17.71%, relative bias <5.87%) in the dosing range of concentrations. The limits of quantification (LOQs) obtained ranged between 0.30 and 1.23ng/ml depending on the analyte. The reliability of the method was proven in passing successfully the German External Quality Assessment Scheme (G-EQUAS). Moreover, the urine from 25 volunteers were analyzed for the determination of glucuro-, sulfo- and free species separately. Phthalate metabolites, parabens and benzophenone-3 were positively detected in almost all urine samples, with detection rates ranging from 40 to 100%. Levels measured ranged from <LOQ to 2207ng/ml varying widely depending on the compound and the individual. In our small participating population, most of the phthalate metabolites were excreted predominately as glucuroconjugated forms while parabens and benzophenone-3 were detected as glucuro- and sulfoconjugated species in variable proportions according to the target compound.
邻苯二甲酸酯、对羟基苯甲酸酯和 2-羟基-4-甲氧基二苯甲酮或苯酮-3 被认为是内分泌干扰化学物质,能够破坏内分泌平衡,因此可能导致一些激素疾病。大量的大规模生物监测研究在超过 75%的普通人群中检测到了这些化合物的生物标志物。为了评估这些化学物质的暴露情况,我们开发了一种基于固相萃取 (SPE) 的分析方法,然后进行超高效液相色谱-串联质谱 (UPLC-MS/MS) 分析,以同时测量 7 种邻苯二甲酸代谢物(单苄基邻苯二甲酸酯、单正丁基邻苯二甲酸酯、单异丁基邻苯二甲酸酯、单-2-乙基己基邻苯二甲酸酯、单-2-乙基-5-羟基己基邻苯二甲酸酯、单-2-乙基-5-氧代己基邻苯二甲酸酯、单乙基邻苯二甲酸酯)、4 种对羟基苯甲酸酯(甲基对羟基苯甲酸酯、乙基对羟基苯甲酸酯、正丙基对羟基苯甲酸酯、正丁基对羟基苯甲酸酯)和苯酮-3 在人尿中的含量。通过不同的酶解反应实现了对未结合物、葡糖苷酸和硫酸结合物的区分。整个过程根据总误差方法进行了验证,结果表明在浓度测定范围内具有线性(回归系数范围为 0.987 至 0.998)和准确性(内部和内部精密度 <17.71%,相对偏差 <5.87%)。根据分析物的不同,定量下限 (LOQ) 范围在 0.30 至 1.23ng/ml 之间。该方法通过成功通过德国外部质量评估计划 (G-EQUAS) 验证了其可靠性。此外,还对 25 名志愿者的尿液进行了分析,以分别确定葡萄糖醛酸、硫酸和游离形式。邻苯二甲酸代谢物、对羟基苯甲酸酯和苯酮-3 在几乎所有尿液样本中均被阳性检测到,检出率在 40%至 100%之间。所测量的水平范围从 <LOQ 到 2207ng/ml 不等,根据化合物和个体的不同而有很大差异。在我们的小参与人群中,大多数邻苯二甲酸代谢物主要以葡萄糖醛酸结合形式排泄,而对羟基苯甲酸酯和苯酮-3 则以不同比例的葡萄糖醛酸和硫酸结合形式检测到。