Modelling ecological risks of antiretroviral drugs in the environment

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dc.contributor.author Ngwenya, Phephile
dc.contributor.author Musee, Ndeke
dc.date.accessioned 2024-05-28T06:00:19Z
dc.date.available 2024-05-28T06:00:19Z
dc.date.issued 2023
dc.description APPENDIX A. SUPPLEMENTARY DATA : Supplementary data to this article can be found online at https://DOI.org/10.1016/j.enceco.2023.06.001. en_US
dc.description.abstract The success of the antiretroviral therapy (ART) programme to manage HIV/AIDS in Sub-Saharan Africa (SSA) has inadvertently led to the release of antiretroviral (ARVs) into the environment. Consequently, ARVs have been detected in different countries across the globe, with the highest measured environmental concentrations in the SSA countries. Herein, we quantified ecological risks of ten regimen ARVs (six and four in first and second regimes, respectively) into environmental matrices in four spatial regions in Eswatini, namely: Manzini, Hhohho, Lubombo, and Shiselweni. Ecological risks (expressed as risk quotient (RQ)) were determined for different geographical regions by comparing the predicted environmental concentrations (PECs) to the predicted no effect concentrations (PNECs). PNECs were derived from ecotoxicological data generated using the Ecological Structure Activity Relationships (ECOSAR) model. PECs of ARVs in surfacewater in the Lubombo and Shiselweni regions were three-fold higher compared to those of the Manzini and Hhohho regions with RQs of three ARVs exceeding 10 (RQ > 10) to three taxa (fish, daphnia, and algae). ARVs of concern to the three taxa were ranked in descending order based on both acute and chronic toxicity based on RQ values as efavirenz (EFV) > lopinavir (LPV) > ritonavir (RTV) (all with RQs > 10). Two second regime ARV drugs (RTV and LPV) posed the highest risks to aquatic taxa though they had the least PECs, but were highly toxic with PNECs <1 μg/L. Due to dearth of toxicity data for ARVs on bacteria, their risks in wastewater (with the exception of TDF) could not be established. Results of this study are the first to quantify risks of ARVs in the environment using a modelling approach. The developed model can therefore serve as a first-tier screening tool. In addition, the results raise the need to examine the likelihood of antiviral resistance of ARVs linked to their high environmental concentrations. en_US
dc.description.department Chemical Engineering en_US
dc.description.librarian am2024 en_US
dc.description.sdg SDG-03:Good heatlh and well-being en_US
dc.description.sdg SDG-11:Sustainable cities and communities en_US
dc.description.sponsorship The Water Research Commission (South Africa). en_US
dc.description.uri http://www.keaipublishing.com/en/journals/environmental-chemistry-and-ecotoxicology/ en_US
dc.identifier.citation Ngwenya, P. & Musee, N. 2023, 'Modelling ecological risks of antiretroviral drugs in the environment', Environmental Chemistry and Ecotoxicology, vol. 5, pp. 145-154. http://dx.DOI.org/10.1016/j.enceco.2023.06.001. en_US
dc.identifier.issn 2141-226X
dc.identifier.other 10.1016/j.enceco.2023.06.001
dc.identifier.uri http://hdl.handle.net/2263/96256
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.rights © 2023 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. This is an open access article under the CCBY-NC-ND license. en_US
dc.subject Risk quotient en_US
dc.subject Aquatic organisms en_US
dc.subject Risk ranking en_US
dc.subject Eswatini en_US
dc.subject Antiretroviral therapy (ART) en_US
dc.subject Antiretroviral (ARV) en_US
dc.subject Sub-Saharan Africa (SSA) en_US
dc.subject Human immunodeficiency virus (HIV) en_US
dc.subject Acquired immune deficiency syndrome (AIDS) en_US
dc.subject Predicted no effect concentrations (PNECs) en_US
dc.subject Predicted environmental concentrations (PECs) en_US
dc.subject SDG-03: Good health and well-being en_US
dc.subject SDG-11: Sustainable cities and communities en_US
dc.title Modelling ecological risks of antiretroviral drugs in the environment en_US
dc.type Article en_US


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