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人体尿液中二苯甲酮和樟脑紫外线过滤剂测定灵敏方法的实施

Implementation of Sensitive Method for Determination of Benzophenone and Camphor UV Filters in Human Urine.

作者信息

Gomersall Veronika, Ciglova Katerina, Pulkrabova Jana

机构信息

Department of Food Analysis and Nutrition, Faculty of Food and Biochemical Technology, University of Chemistry and Technology, Prague, Technicka 3, 166 28 Prague, Czech Republic.

出版信息

Toxics. 2024 Nov 21;12(12):837. doi: 10.3390/toxics12120837.

DOI:10.3390/toxics12120837
PMID:39771052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11679341/
Abstract

The level of the human body's burden of benzophenone and camphor ultraviolet (UV) filters can be estimated from their urinary levels. The present study describes the implementations and validation of the sensitive analytical method for the analysis of seven benzophenone and two camphor UV filters in urine. Sample preparation includes overnight enzymatic hydrolysis and ethyl acetate extraction followed by purification by dispersive solid-phase extraction using a sorbent Z-Sep. For the analysis, ultra-high performance liquid chromatography coupled with tandem mass spectrometry was used. Validation was performed using a Standard Reference Material 3673 and an artificially contaminated urine sample. Target analyte recoveries ranged from 79-113% with repeatability expressed as a relative standard deviation of 2-15%. The limits of quantification were between 0.001 and 0.100 ng/mL in urine. This method was subsequently applied to examine the urine samples collected from Czech women. The analytes benzophenone-1 and 4-hydroxy-benzophenone were the most common analytes present in 100% of the samples, whereas benzophenone-3 was quantified in only 90% of the urine samples. The other four determined benzophenone derivatives were quantified in ≤33% of the samples. The derivatives of camphor were not detected in any samples. This method could be applied in biomonitoring studies.

摘要

人体二苯甲酮和樟脑紫外线(UV)滤光剂的负荷水平可通过其尿液水平进行估算。本研究描述了用于分析尿液中七种二苯甲酮和两种樟脑紫外线滤光剂的灵敏分析方法的实施与验证。样品制备包括过夜酶解和乙酸乙酯萃取,随后使用吸附剂Z-Sep通过分散固相萃取进行纯化。分析采用超高效液相色谱-串联质谱联用。使用标准参考物质3673和人工污染的尿液样品进行验证。目标分析物回收率在79%-113%之间,重复性以相对标准偏差2%-15%表示。尿液中的定量限在0.001至0.100 ng/mL之间。该方法随后应用于检测从捷克女性收集的尿液样本。分析物二苯甲酮-1和4-羟基二苯甲酮是100%的样本中最常见的分析物,而二苯甲酮-3仅在90%的尿液样本中被定量。其他四种测定的二苯甲酮衍生物在≤33%的样本中被定量。在任何样本中均未检测到樟脑衍生物。该方法可应用于生物监测研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/7a8e1b06dc93/toxics-12-00837-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/3528a2780195/toxics-12-00837-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/386923d9faee/toxics-12-00837-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/2ac23850f44b/toxics-12-00837-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/080c855586d7/toxics-12-00837-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/74bf0d096d6b/toxics-12-00837-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/7a8e1b06dc93/toxics-12-00837-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/3528a2780195/toxics-12-00837-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/386923d9faee/toxics-12-00837-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/2ac23850f44b/toxics-12-00837-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/080c855586d7/toxics-12-00837-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/74bf0d096d6b/toxics-12-00837-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b667/11679341/7a8e1b06dc93/toxics-12-00837-g006.jpg

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