Profiling and comparison of toxicant metabolites in hair and urine using a mass spectrometry-based metabolomic data processing method

毒物 尿 化学 代谢物 色谱法 邻苯二甲酸盐 代谢组学 代谢组 生物化学 毒性 有机化学
作者
Chia-Lung Shih,Hsin-Yi Wu,Pao-Mei Liao,Jen-Yi Hsu,Chia-Yun Tsao,Victor G. Zgoda,Pao‐Chi Liao
出处
期刊:Analytica Chimica Acta [Elsevier]
卷期号:1052: 84-95 被引量:16
标识
DOI:10.1016/j.aca.2018.11.009
摘要

Urine and hair are used for assessing human exposure to toxicants. Urine tests can show acute toxicant exposure. Hair analysis can be used to determine chronic toxicant exposure after months to years; however, compared to urine, hair analysis in exposure assessments is much less frequently investigated. Urine and hair are different matrices, and their mechanisms of toxicant metabolite incorporation are different. The toxicant metabolites present in urine and hair may also be different. To clarify this issue, a procedure was developed to identify toxicant metabolites in rat samples using a mass spectrometry-based metabolomic data processing method. Di-(2-propylheptyl) phthalate (DPHP), an industrial plasticizer, was used as the model toxicant. The developed procedure identified not only known DPHP metabolites (mono-(propyl-6-oxo-heptyl) phthalate, mono-(propyl-6-hydroxyheptyl) phthalate, and mono-(propyl-6-carboxyhexyl) phthalate) but also novel metabolites that were structurally related to DPHP in the rat samples, indicating that the developed procedure successfully identified toxicant metabolites in in vivo samples. Among the 62 tentative metabolites identified from the 7th-day urine and the 28th-day hair samples, 33 were detected in only the urine samples, 19 were detected in only the hair samples, and 10 were identified in both the urine and hair samples. A total of 15 out of the 62 metabolites were confirmed as DPHP structure-related metabolites based on MS/MS analysis. Among the 15 DPHP structure-related metabolites, only 2 metabolites were present in both the urine and hair samples. These results suggested that the metabolites identified in urine could not be applied to exposure assessments based on hair analysis.
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