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COVID-19 related antiviral drugs are less adsorbable on sediment under alkaline and high cation conditions
The COVID-19 pandemic resulted in unprecedented usage and elevated environmental concentrations of antiviral drugs. However, very limited studies have reported their sorption characteristics on environmental matrices. This study investigated the sorption of six COVID-19 related antivirals on Taihu L...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140464/ https://www.ncbi.nlm.nih.gov/pubmed/37120016 http://dx.doi.org/10.1016/j.scitotenv.2023.163736 |
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author | Xu, Xin Zhu, Rong Zhang, Yun Bartelt-Hunt, Shannon L. Zou, Hua Chen, Chen |
author_facet | Xu, Xin Zhu, Rong Zhang, Yun Bartelt-Hunt, Shannon L. Zou, Hua Chen, Chen |
author_sort | Xu, Xin |
collection | PubMed |
description | The COVID-19 pandemic resulted in unprecedented usage and elevated environmental concentrations of antiviral drugs. However, very limited studies have reported their sorption characteristics on environmental matrices. This study investigated the sorption of six COVID-19 related antivirals on Taihu Lake sediment with varied aqueous chemistry. Results showed that the sorption isotherms for arbidol (ABD), oseltamivir (OTV), and ritonavir (RTV) were linear, while the Freundlich model was the best-fit for ribavirin (RBV) and the Langmuir model for favipiravir (FPV) and remdesivir (RDV). Their distribution coefficient, K(d,) varied between 5.051 L/kg to 248.6 L/kg with the sorption capacities ranked as FPV > RDV > ABD > RTV > OTV > RBV. Alkaline conditions (pH 9) and elevated cation strength (0.05 M to 0.1 M) decreased the sorption capacities of the sediment for these drugs. Thermodynamic analysis revealed that the spontaneous sorption of RDV, ABD, and RTV was between physisorption and chemisorption while FPV, RBV, and OTV were mainly physisorption. Functional groups related to hydrogen bonds, π – π interaction, and surface complexation were implicated in the sorption processes. These findings enhance our understanding about the environmental fate of COVID-19 related antivirals and provide basic data for predicting their distribution and risk in the environment. |
format | Online Article Text |
id | pubmed-10140464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101404642023-04-28 COVID-19 related antiviral drugs are less adsorbable on sediment under alkaline and high cation conditions Xu, Xin Zhu, Rong Zhang, Yun Bartelt-Hunt, Shannon L. Zou, Hua Chen, Chen Sci Total Environ Article The COVID-19 pandemic resulted in unprecedented usage and elevated environmental concentrations of antiviral drugs. However, very limited studies have reported their sorption characteristics on environmental matrices. This study investigated the sorption of six COVID-19 related antivirals on Taihu Lake sediment with varied aqueous chemistry. Results showed that the sorption isotherms for arbidol (ABD), oseltamivir (OTV), and ritonavir (RTV) were linear, while the Freundlich model was the best-fit for ribavirin (RBV) and the Langmuir model for favipiravir (FPV) and remdesivir (RDV). Their distribution coefficient, K(d,) varied between 5.051 L/kg to 248.6 L/kg with the sorption capacities ranked as FPV > RDV > ABD > RTV > OTV > RBV. Alkaline conditions (pH 9) and elevated cation strength (0.05 M to 0.1 M) decreased the sorption capacities of the sediment for these drugs. Thermodynamic analysis revealed that the spontaneous sorption of RDV, ABD, and RTV was between physisorption and chemisorption while FPV, RBV, and OTV were mainly physisorption. Functional groups related to hydrogen bonds, π – π interaction, and surface complexation were implicated in the sorption processes. These findings enhance our understanding about the environmental fate of COVID-19 related antivirals and provide basic data for predicting their distribution and risk in the environment. Elsevier B.V. 2023-07-20 2023-04-28 /pmc/articles/PMC10140464/ /pubmed/37120016 http://dx.doi.org/10.1016/j.scitotenv.2023.163736 Text en © 2023 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Xu, Xin Zhu, Rong Zhang, Yun Bartelt-Hunt, Shannon L. Zou, Hua Chen, Chen COVID-19 related antiviral drugs are less adsorbable on sediment under alkaline and high cation conditions |
title | COVID-19 related antiviral drugs are less adsorbable on sediment under alkaline and high cation conditions |
title_full | COVID-19 related antiviral drugs are less adsorbable on sediment under alkaline and high cation conditions |
title_fullStr | COVID-19 related antiviral drugs are less adsorbable on sediment under alkaline and high cation conditions |
title_full_unstemmed | COVID-19 related antiviral drugs are less adsorbable on sediment under alkaline and high cation conditions |
title_short | COVID-19 related antiviral drugs are less adsorbable on sediment under alkaline and high cation conditions |
title_sort | covid-19 related antiviral drugs are less adsorbable on sediment under alkaline and high cation conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10140464/ https://www.ncbi.nlm.nih.gov/pubmed/37120016 http://dx.doi.org/10.1016/j.scitotenv.2023.163736 |
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