Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/89735
Title: Chemical isotope labeling exposome (CIL-EXPOSOME) : one high-throughput platform for human urinary global exposome characterization
Authors: Jia, Shenglan
Xu, Tengfei
Huan, Tao
Chong, Maria
Liu, Min
Fang, Wenjuan
Fang, Mingliang
Keywords: Exposome
DRNTU::Science::Chemistry
Chemical Isotope
Issue Date: 2019
Source: Jia, S., Xu, T., Huan, T., Chong, M., Liu, M., Fang, W., & Fang, M. (2019). Chemical isotope labeling exposome (CIL-EXPOSOME) : one high-throughput platform for human urinary global exposome characterization. Environmental Science & Technology, 53(9), 5445-5453. doi:10.1021/acs.est.9b00285
Series/Report no.: Environmental Science & Technology
Abstract: Human exposure to hundreds of chemicals, a primary component of the exposome, has been associated with many diseases. Urinary biomarkers of these chemicals are commonly monitored to quantify their exposure. However, because of low concentrations and the great variability in physicochemical properties of exposure biomarkers, exposome research has been limited by low-throughput and costly methods. Here, we developed a sensitive and high-throughput exposome analytical platform (CIL-EXPOSOME) by isotopically labeling urinary biomarkers with common functional groups (phenolic hydroxyl/carboxyl/primary amine). After a simple cleanup, we used mass spectrometry to perform a screening for both targeted and untargeted biomarkers, which was further processed by an automatic computational pipeline method for qualification and quantification. This platform has effectively introduced an isotope tag for the absolute quantification of biomarkers and has improved sensitivity of 2−1184 fold compared to existing methods. For putative identification, we built a database of 818 urinary biomarkers with MS/MS fragmentation information from either standards or in silico predictions. Using this platform, we have found 671 urinary exposure biomarker candidates from a 2 mL pooled urine sample. The exposome data acquisition and analysis time has also been greatly shortened. The results showed that CILEXPOSOME is a useful tool for global exposome analysis of complex samples.
URI: https://hdl.handle.net/10356/89735
http://hdl.handle.net/10220/48841
DOI: 10.1021/acs.est.9b00285
Rights: This document is the Accepted Manuscript version of a Published Work that appeared in final form in Environmental Science & Technology, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.est.9b00285
Fulltext Permission: embargo_20200410
Fulltext Availability: With Fulltext
Appears in Collections:CEE Journal Articles
NEWRI Journal Articles

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