Xianyin Zhang , Xiangping Liu , Jie Xu , Wenfang Sun , Xin Xu , Wenliang Ji
{"title":"超高效液相色谱串联质谱法同时测定人体尿液中11种有机磷阻燃剂和6种代谢物","authors":"Xianyin Zhang , Xiangping Liu , Jie Xu , Wenfang Sun , Xin Xu , Wenliang Ji","doi":"10.1016/j.jpba.2025.117162","DOIUrl":null,"url":null,"abstract":"<div><div>Organophosphorus flame retardants (OPFRs) are widely used chemicals with significant health risks to humans. OPFRs are metabolized and excreted primarily through urine, making urine a key matrix for assessing human exposure levels. Therefore, this study developed a method combining the Quick, Easy, Cheap, Effective, Rugged, Safe (QuEChERS) approach with ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) for the simultaneous determination of 11 OPFRs and 6 organophosphorus flame retardant metabolites (mOPFRs) in human urine. All target compounds exhibited excellent linearity, with correlation coefficients (<em>r</em>²) exceeding 0.9988. The limits of detection (LODs) and the limits of quantification (LOQs) ranged from 0.01 ng/mL to 0.05 ng/mL and 0.03 ng/mL to 0.16 ng/mL, respectively. Except for tricresyl phosphate (<50 %), the spiked recoveries for the other target compounds were 51.4–117 %, 52.4–100 %, 63.9–128 %, and 89.0–112 % at four concentration levels. All analytes showed intra-day and inter-day precision with relative standard deviations (<em>RSDs</em>) of 0.8–18.8 % and 1.4–12.2 %, respectively. Analysis of children’s urine revealed distinct metabolic patterns: triphenyl phosphate and tris(1,3-dichloro-2-propyl) phosphate were not detected, while their metabolites, diphenyl phosphate and bis(1,3-dichloro-2-propyl) phosphate, were found in the urine. In contrast, tris(2-butoxyethyl) phosphate, tributyl phosphate, tri(2-chloroethyl) phosphate, and tris(1-chloro-2-propyl) phosphate suggested possible co-occurrence of parent compounds and metabolites. The developed method is simple, sensitive and robust, and has the advantage of high throughput for screening 17 targets including parent compounds and metabolites. These features make it suitable for assessing the exposure risk of OPFRs in urine.</div></div>","PeriodicalId":16685,"journal":{"name":"Journal of pharmaceutical and biomedical analysis","volume":"267 ","pages":"Article 117162"},"PeriodicalIF":3.1000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Simultaneous determination of 11 organophosphorus flame retardants and 6 metabolites in human urine by ultra-performance liquid chromatography tandem mass spectrometry\",\"authors\":\"Xianyin Zhang , Xiangping Liu , Jie Xu , Wenfang Sun , Xin Xu , Wenliang Ji\",\"doi\":\"10.1016/j.jpba.2025.117162\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Organophosphorus flame retardants (OPFRs) are widely used chemicals with significant health risks to humans. OPFRs are metabolized and excreted primarily through urine, making urine a key matrix for assessing human exposure levels. Therefore, this study developed a method combining the Quick, Easy, Cheap, Effective, Rugged, Safe (QuEChERS) approach with ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) for the simultaneous determination of 11 OPFRs and 6 organophosphorus flame retardant metabolites (mOPFRs) in human urine. All target compounds exhibited excellent linearity, with correlation coefficients (<em>r</em>²) exceeding 0.9988. The limits of detection (LODs) and the limits of quantification (LOQs) ranged from 0.01 ng/mL to 0.05 ng/mL and 0.03 ng/mL to 0.16 ng/mL, respectively. Except for tricresyl phosphate (<50 %), the spiked recoveries for the other target compounds were 51.4–117 %, 52.4–100 %, 63.9–128 %, and 89.0–112 % at four concentration levels. All analytes showed intra-day and inter-day precision with relative standard deviations (<em>RSDs</em>) of 0.8–18.8 % and 1.4–12.2 %, respectively. Analysis of children’s urine revealed distinct metabolic patterns: triphenyl phosphate and tris(1,3-dichloro-2-propyl) phosphate were not detected, while their metabolites, diphenyl phosphate and bis(1,3-dichloro-2-propyl) phosphate, were found in the urine. In contrast, tris(2-butoxyethyl) phosphate, tributyl phosphate, tri(2-chloroethyl) phosphate, and tris(1-chloro-2-propyl) phosphate suggested possible co-occurrence of parent compounds and metabolites. The developed method is simple, sensitive and robust, and has the advantage of high throughput for screening 17 targets including parent compounds and metabolites. These features make it suitable for assessing the exposure risk of OPFRs in urine.</div></div>\",\"PeriodicalId\":16685,\"journal\":{\"name\":\"Journal of pharmaceutical and biomedical analysis\",\"volume\":\"267 \",\"pages\":\"Article 117162\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of pharmaceutical and biomedical analysis\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0731708525005035\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of pharmaceutical and biomedical analysis","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0731708525005035","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Simultaneous determination of 11 organophosphorus flame retardants and 6 metabolites in human urine by ultra-performance liquid chromatography tandem mass spectrometry
Organophosphorus flame retardants (OPFRs) are widely used chemicals with significant health risks to humans. OPFRs are metabolized and excreted primarily through urine, making urine a key matrix for assessing human exposure levels. Therefore, this study developed a method combining the Quick, Easy, Cheap, Effective, Rugged, Safe (QuEChERS) approach with ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) for the simultaneous determination of 11 OPFRs and 6 organophosphorus flame retardant metabolites (mOPFRs) in human urine. All target compounds exhibited excellent linearity, with correlation coefficients (r²) exceeding 0.9988. The limits of detection (LODs) and the limits of quantification (LOQs) ranged from 0.01 ng/mL to 0.05 ng/mL and 0.03 ng/mL to 0.16 ng/mL, respectively. Except for tricresyl phosphate (<50 %), the spiked recoveries for the other target compounds were 51.4–117 %, 52.4–100 %, 63.9–128 %, and 89.0–112 % at four concentration levels. All analytes showed intra-day and inter-day precision with relative standard deviations (RSDs) of 0.8–18.8 % and 1.4–12.2 %, respectively. Analysis of children’s urine revealed distinct metabolic patterns: triphenyl phosphate and tris(1,3-dichloro-2-propyl) phosphate were not detected, while their metabolites, diphenyl phosphate and bis(1,3-dichloro-2-propyl) phosphate, were found in the urine. In contrast, tris(2-butoxyethyl) phosphate, tributyl phosphate, tri(2-chloroethyl) phosphate, and tris(1-chloro-2-propyl) phosphate suggested possible co-occurrence of parent compounds and metabolites. The developed method is simple, sensitive and robust, and has the advantage of high throughput for screening 17 targets including parent compounds and metabolites. These features make it suitable for assessing the exposure risk of OPFRs in urine.
期刊介绍:
This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome.
Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.