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Identification and structural elucidation of ozonation transformation products of estrone

BACKGROUND: Quantitative methods for the analysis of contaminants of emerging concern (CECs) are abundant in the scientific literature. However, there are few reports on systematic methods of identification and structural identification of transformation products. For this reason, a new method based...

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Autores principales: Segura, Pedro Alejandro, Kaplan, Pearl, Yargeau, Viviane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3643888/
https://www.ncbi.nlm.nih.gov/pubmed/23618537
http://dx.doi.org/10.1186/1752-153X-7-74
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author Segura, Pedro Alejandro
Kaplan, Pearl
Yargeau, Viviane
author_facet Segura, Pedro Alejandro
Kaplan, Pearl
Yargeau, Viviane
author_sort Segura, Pedro Alejandro
collection PubMed
description BACKGROUND: Quantitative methods for the analysis of contaminants of emerging concern (CECs) are abundant in the scientific literature. However, there are few reports on systematic methods of identification and structural identification of transformation products. For this reason, a new method based on high-resolution mass spectrometry and differential analysis was developed in order to facilitate and accelerate the process of identification and structural elucidation of transformation products CECs. This method was applied to the study of ozonation transformation products (OTPs) of the natural hormone estrone (E1). RESULTS: A control compare trend experiment consisting in the comparison of a control sample to several samples having been exposed to decreasing concentrations of O(3(aq)) indicated that 593 peaks could be associated with OTPs. After applying various filters to remove background noise, sample contaminants and signal spikes, this data set was reduced to 16 candidate peaks. By inspection of the shape of these peaks, only two compounds OTP-276 (m/z 275.12930) and OTP-318 (m/z 317.14008) were considered as good candidates for further study. Multi-stage tandem mass spectrometry (MS(n)) experiments of SPE extracts of the ozonated samples of E1 and of a deuterium-labeled analogue (E1-d(4)) showed that OTP-276 and OTP-318 had carboxylic acid and hydroxyl functional groups, as previously reported for OTPs of other hormones. Structures for these two compounds were proposed based on their MS(n) spectra. CONCLUSION: These results indicate that the method proposed is a systematic and rapid approach to study transformation products of CECs.
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spelling pubmed-36438882013-05-04 Identification and structural elucidation of ozonation transformation products of estrone Segura, Pedro Alejandro Kaplan, Pearl Yargeau, Viviane Chem Cent J Research Article BACKGROUND: Quantitative methods for the analysis of contaminants of emerging concern (CECs) are abundant in the scientific literature. However, there are few reports on systematic methods of identification and structural identification of transformation products. For this reason, a new method based on high-resolution mass spectrometry and differential analysis was developed in order to facilitate and accelerate the process of identification and structural elucidation of transformation products CECs. This method was applied to the study of ozonation transformation products (OTPs) of the natural hormone estrone (E1). RESULTS: A control compare trend experiment consisting in the comparison of a control sample to several samples having been exposed to decreasing concentrations of O(3(aq)) indicated that 593 peaks could be associated with OTPs. After applying various filters to remove background noise, sample contaminants and signal spikes, this data set was reduced to 16 candidate peaks. By inspection of the shape of these peaks, only two compounds OTP-276 (m/z 275.12930) and OTP-318 (m/z 317.14008) were considered as good candidates for further study. Multi-stage tandem mass spectrometry (MS(n)) experiments of SPE extracts of the ozonated samples of E1 and of a deuterium-labeled analogue (E1-d(4)) showed that OTP-276 and OTP-318 had carboxylic acid and hydroxyl functional groups, as previously reported for OTPs of other hormones. Structures for these two compounds were proposed based on their MS(n) spectra. CONCLUSION: These results indicate that the method proposed is a systematic and rapid approach to study transformation products of CECs. BioMed Central 2013-04-23 /pmc/articles/PMC3643888/ /pubmed/23618537 http://dx.doi.org/10.1186/1752-153X-7-74 Text en Copyright © 2013 Segura et al.; licensee Chemistry Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Segura, Pedro Alejandro
Kaplan, Pearl
Yargeau, Viviane
Identification and structural elucidation of ozonation transformation products of estrone
title Identification and structural elucidation of ozonation transformation products of estrone
title_full Identification and structural elucidation of ozonation transformation products of estrone
title_fullStr Identification and structural elucidation of ozonation transformation products of estrone
title_full_unstemmed Identification and structural elucidation of ozonation transformation products of estrone
title_short Identification and structural elucidation of ozonation transformation products of estrone
title_sort identification and structural elucidation of ozonation transformation products of estrone
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3643888/
https://www.ncbi.nlm.nih.gov/pubmed/23618537
http://dx.doi.org/10.1186/1752-153X-7-74
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