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Spatiotemporal Distribution and Analysis of Organophosphate Flame Retardants in the Environmental Systems: A Review

In recent times, there has been a cumulative apprehension regarding organophosphate flame retardants (OPFRs) owing to their high manufacturing and usage after brominated flame retardants were strictly regulated and banned from being distributed and used in many countries. OPFRs are known as the main...

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Autores principales: Bika, Sinozuko Hope, Adeniji, Abiodun Olagoke, Okoh, Anthony Ifeanyi, Okoh, Omobola Oluranti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780022/
https://www.ncbi.nlm.nih.gov/pubmed/35056888
http://dx.doi.org/10.3390/molecules27020573
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author Bika, Sinozuko Hope
Adeniji, Abiodun Olagoke
Okoh, Anthony Ifeanyi
Okoh, Omobola Oluranti
author_facet Bika, Sinozuko Hope
Adeniji, Abiodun Olagoke
Okoh, Anthony Ifeanyi
Okoh, Omobola Oluranti
author_sort Bika, Sinozuko Hope
collection PubMed
description In recent times, there has been a cumulative apprehension regarding organophosphate flame retardants (OPFRs) owing to their high manufacturing and usage after brominated flame retardants were strictly regulated and banned from being distributed and used in many countries. OPFRs are known as the main organic pollutants in the terrestrial and aquatic environment. They are very dangerous to humans, plants and animals. They are also carcinogenic and some have been implicated in neurodevelopmental and fertility challenges. OPFRs are distributed into the environment through a number of processes, including the usage, improper disposal and production of materials. The solid phase extraction (SPE) method is suggested for the extraction of OPFRs from water samples since it provides high quality recoveries ranging from 67% to 105% and relative standard deviations (RSDs) below 20%. In the same vein, microwave-assisted extraction (MAE) is highly advocated for the extraction of OPFRs from sediment/soil. Recoveries in the range of 78% to 105% and RSDs ranging from 3% to 8% have been reported. Hence, it is a faster method of extraction for solid samples and only demands a reduced amount of solvent, unlike other methods. The extract of OPFRs from various matrices is then followed by a clean-up of the extract using a silica gel packed column followed by the quantification of compounds by gas chromatography coupled with a mass spectrometer (GC–MS) or a flame ionization detector (GC-FID). In this paper, different analytical methods for the evaluation of OPFRs in different environmental samples are reviewed. The effects and toxicities of these contaminants on humans and other organisms are also discussed.
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spelling pubmed-87800222022-01-22 Spatiotemporal Distribution and Analysis of Organophosphate Flame Retardants in the Environmental Systems: A Review Bika, Sinozuko Hope Adeniji, Abiodun Olagoke Okoh, Anthony Ifeanyi Okoh, Omobola Oluranti Molecules Review In recent times, there has been a cumulative apprehension regarding organophosphate flame retardants (OPFRs) owing to their high manufacturing and usage after brominated flame retardants were strictly regulated and banned from being distributed and used in many countries. OPFRs are known as the main organic pollutants in the terrestrial and aquatic environment. They are very dangerous to humans, plants and animals. They are also carcinogenic and some have been implicated in neurodevelopmental and fertility challenges. OPFRs are distributed into the environment through a number of processes, including the usage, improper disposal and production of materials. The solid phase extraction (SPE) method is suggested for the extraction of OPFRs from water samples since it provides high quality recoveries ranging from 67% to 105% and relative standard deviations (RSDs) below 20%. In the same vein, microwave-assisted extraction (MAE) is highly advocated for the extraction of OPFRs from sediment/soil. Recoveries in the range of 78% to 105% and RSDs ranging from 3% to 8% have been reported. Hence, it is a faster method of extraction for solid samples and only demands a reduced amount of solvent, unlike other methods. The extract of OPFRs from various matrices is then followed by a clean-up of the extract using a silica gel packed column followed by the quantification of compounds by gas chromatography coupled with a mass spectrometer (GC–MS) or a flame ionization detector (GC-FID). In this paper, different analytical methods for the evaluation of OPFRs in different environmental samples are reviewed. The effects and toxicities of these contaminants on humans and other organisms are also discussed. MDPI 2022-01-17 /pmc/articles/PMC8780022/ /pubmed/35056888 http://dx.doi.org/10.3390/molecules27020573 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Bika, Sinozuko Hope
Adeniji, Abiodun Olagoke
Okoh, Anthony Ifeanyi
Okoh, Omobola Oluranti
Spatiotemporal Distribution and Analysis of Organophosphate Flame Retardants in the Environmental Systems: A Review
title Spatiotemporal Distribution and Analysis of Organophosphate Flame Retardants in the Environmental Systems: A Review
title_full Spatiotemporal Distribution and Analysis of Organophosphate Flame Retardants in the Environmental Systems: A Review
title_fullStr Spatiotemporal Distribution and Analysis of Organophosphate Flame Retardants in the Environmental Systems: A Review
title_full_unstemmed Spatiotemporal Distribution and Analysis of Organophosphate Flame Retardants in the Environmental Systems: A Review
title_short Spatiotemporal Distribution and Analysis of Organophosphate Flame Retardants in the Environmental Systems: A Review
title_sort spatiotemporal distribution and analysis of organophosphate flame retardants in the environmental systems: a review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780022/
https://www.ncbi.nlm.nih.gov/pubmed/35056888
http://dx.doi.org/10.3390/molecules27020573
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