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Phototransformation of Amlodipine: Degradation Kinetics and Identification of Its Photoproducts

Nowadays, monitoring focuses on the primary compounds and does not include degradation products formed during various biological and chemical processes. Transformation products may have the same effects to human health and the environment or sometimes they can be more toxic than the parent compound....

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Autores principales: Jakimska, Anna, Śliwka-Kaszyńska, Magdalena, Nagórski, Piotr, Namieśnik, Jacek, Kot-Wasik, Agata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184881/
https://www.ncbi.nlm.nih.gov/pubmed/25279815
http://dx.doi.org/10.1371/journal.pone.0109206
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author Jakimska, Anna
Śliwka-Kaszyńska, Magdalena
Nagórski, Piotr
Namieśnik, Jacek
Kot-Wasik, Agata
author_facet Jakimska, Anna
Śliwka-Kaszyńska, Magdalena
Nagórski, Piotr
Namieśnik, Jacek
Kot-Wasik, Agata
author_sort Jakimska, Anna
collection PubMed
description Nowadays, monitoring focuses on the primary compounds and does not include degradation products formed during various biological and chemical processes. Transformation products may have the same effects to human health and the environment or sometimes they can be more toxic than the parent compound. Unfortunately, knowledge about the formation of degradation products is still limited, however, can be very important for the environmental risk assessment. Firstly, the photodegradation kinetic of amlodipine was investigated in two experimental conditions: during the exposure to solar radiation and during the exposure to the light emitted by the xenon lamp. In all cases degradation of amlodipine followed a pseudo-first-order kinetics. In the next step, identification of transformation products of amlodipine formed during the exposure to xenon lamp irradiation was performed using ultra high performance liquid chromatography quadrupole time-of-flight mass spectrometry (UHPLC-QTOF-MS). As a result sixteen photoproducts were identified, their structures were elucidated and ultimately the transformation pathway was proposed. Fifteen compounds (out of 16 photoproducts) were newly identified and reported here for the first time; some of those compounds were formed from the first photoproduct, amlodipine pyridine derivative. Several analytes were formed only in acidic or basic conditions. Furthermore, the occurrence of amlodipine and its identified degradation products was investigated in environmental waters. Only one out of 16 compounds was found in wastewater effluent. The possibility of the sorption of examined analytes to sewage sludge particles was discussed based on QSAR.
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spelling pubmed-41848812014-10-07 Phototransformation of Amlodipine: Degradation Kinetics and Identification of Its Photoproducts Jakimska, Anna Śliwka-Kaszyńska, Magdalena Nagórski, Piotr Namieśnik, Jacek Kot-Wasik, Agata PLoS One Research Article Nowadays, monitoring focuses on the primary compounds and does not include degradation products formed during various biological and chemical processes. Transformation products may have the same effects to human health and the environment or sometimes they can be more toxic than the parent compound. Unfortunately, knowledge about the formation of degradation products is still limited, however, can be very important for the environmental risk assessment. Firstly, the photodegradation kinetic of amlodipine was investigated in two experimental conditions: during the exposure to solar radiation and during the exposure to the light emitted by the xenon lamp. In all cases degradation of amlodipine followed a pseudo-first-order kinetics. In the next step, identification of transformation products of amlodipine formed during the exposure to xenon lamp irradiation was performed using ultra high performance liquid chromatography quadrupole time-of-flight mass spectrometry (UHPLC-QTOF-MS). As a result sixteen photoproducts were identified, their structures were elucidated and ultimately the transformation pathway was proposed. Fifteen compounds (out of 16 photoproducts) were newly identified and reported here for the first time; some of those compounds were formed from the first photoproduct, amlodipine pyridine derivative. Several analytes were formed only in acidic or basic conditions. Furthermore, the occurrence of amlodipine and its identified degradation products was investigated in environmental waters. Only one out of 16 compounds was found in wastewater effluent. The possibility of the sorption of examined analytes to sewage sludge particles was discussed based on QSAR. Public Library of Science 2014-10-03 /pmc/articles/PMC4184881/ /pubmed/25279815 http://dx.doi.org/10.1371/journal.pone.0109206 Text en © 2014 Jakimska et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jakimska, Anna
Śliwka-Kaszyńska, Magdalena
Nagórski, Piotr
Namieśnik, Jacek
Kot-Wasik, Agata
Phototransformation of Amlodipine: Degradation Kinetics and Identification of Its Photoproducts
title Phototransformation of Amlodipine: Degradation Kinetics and Identification of Its Photoproducts
title_full Phototransformation of Amlodipine: Degradation Kinetics and Identification of Its Photoproducts
title_fullStr Phototransformation of Amlodipine: Degradation Kinetics and Identification of Its Photoproducts
title_full_unstemmed Phototransformation of Amlodipine: Degradation Kinetics and Identification of Its Photoproducts
title_short Phototransformation of Amlodipine: Degradation Kinetics and Identification of Its Photoproducts
title_sort phototransformation of amlodipine: degradation kinetics and identification of its photoproducts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184881/
https://www.ncbi.nlm.nih.gov/pubmed/25279815
http://dx.doi.org/10.1371/journal.pone.0109206
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