Evidence map›Paper›PMID 38877147›Full record

ArticleAnalytical and bioanalytical chemistry2024

Biomonitoring urinary organophosphorus flame retardant metabolites by liquid-liquid extraction and ultra-high performance liquid chromatography-tandem mass spectrometry and their association with oxidative stress.

Yongxian Li, Yingyi Dai, Xinni Luo, Lin Zhang, Jun Yuan, Lei Tan

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Article in Analytical and bioanalytical chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yongxian LiGuangzhou Center for Disease Control and Prevention, Guangzhou, 510440, China.
Yingyi DaiGuangzhou Center for Disease Control and Prevention, Guangzhou, 510440, China.
Xinni LuoAffiliated Brain Hospital of Guangzhou Medical University, Guangzhou, 510370, China.
Lin ZhangGuangzhou Center for Disease Control and Prevention, Guangzhou, 510440, China.
Jun YuanGuangzhou Center for Disease Control and Prevention, Guangzhou, 510440, China.
Lei TanGuangzhou Center for Disease Control and Prevention, Guangzhou, 510440, China. jsutanlei@gmail.com.

Funding

National Natural Science Foundation of China 82273682
6 · The paper itself

Abstract

Organophosphate flame retardants (OPFRs) are widely used as substitutes for traditional brominated flame retardants, necessitating a reliable and sensitive method for biomonitoring their urinary metabolites to assess human exposure. This study conducted biomonitoring of 10 metabolites of OPFRs in 152 adults and assessed their association with oxidative stress biomarkers 8-hydroxydeoxyguanosine and 8-hydroxyguanosine. Urinary metabolites of OPFRs were released via enzymatic deconjugation. The addition of sodium chloride to the urine samples increases the ionic strength, inducing a salting-out effect that reduces the solubility of these compounds, thereby facilitating their extraction with a mixture of ethyl acetate and acetonitrile. Then, the metabolites of OPFRs were quantified by ultra-high performance liquid chromatography-tandem mass spectrometry, and we validated the method for linear range, precision, matrix effect, and method detection limit. The detection limit of the metabolites of OPFRs ranged from 0.01 to 0.2 μg/L, and these metabolites were detected with high frequencies ranging from 25.0 to 98.68% in the urine samples. The concentration of bis (2-chloroethyl) phosphate was significantly higher in males than in females, with the geometric mean concentration of 0.88 μg/L for males and 0.53 μg/L for females, respectively. Spearman correlation analysis revealed weak but statistically significant positive correlations among the urinary metabolites. Bayesian kernel machine regression analysis showed a significant positive association between elevated urinary concentrations of metabolites of OPFRs and increased oxidative stress levels. Di-n-butyl phosphate was identified as the metabolite that significantly contributed to the elevated level of 8-hydroxyguanosine.

Indexed as

Biological MonitoringFlame RetardantsLimit of DetectionLiquid-Liquid ExtractionOrganophosphorus CompoundsOxidative StressTandem Mass SpectrometryAdultBiomarkersChromatography, High Pressure LiquidFemaleHumansMaleMiddle AgedYoung AdultBiomarkersFlame RetardantsOrganophosphorus CompoundsHuman biomonitoringLiquid–liquid extractionOrganophosphate flame retardantsOxidative stressUltra-high performance liquid chromatography-tandem mass spectrometry

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.