Events8th International Electronic Conference on Medicinal Chemistry
Published
This submission belongs to the session S8. Pharmaceutical development of the event 8th International Electronic Conference on Medicinal Chemistry
Published date
01 Nov, 2022
Academic Editor
author-avatarMaria Emília Sousa
Citation
Cátia Venâncio, Bruna Monteiro, Rafael Francisco, Márcia Neves, Mara G. Freire, Ana Catarina A. Sousa, Isabel Lopes, Ecotoxicological tools to assess cytostatics effects in freshwater environments: in the aid of drugs prioritization, in Proceedings of 8th International Electronic Conference on Medicinal Chemistry, 1 November–30 November 2022, MDPI: Basel, Switzerland, doi: 10.3390/ECMC2022-13246
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Ecotoxicological tools to assess cytostatics effects in freshwater environments: in the aid of drugs prioritization

Bruna Monteiro 2
Rafael Francisco 3
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1. CESAM-Centre for Environmental and Marine Studies, University of Aveiro, 3810-193 Aveiro, Portugal, Portugal
2. Department of Biology, University of Aveiro, 3810-193 Aveiro, Portugal
3. CICECO, Aveiro Institute of Materials, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal
4. CESAM-Centre for Environmental and Marine Studies, University of Aveiro, 3810-193 Aveiro, Portugal
Abstract

Given the growing number of cancer diseases, new cytostatic drugs are approved daily, often with concomitant development or refinement of some of these drugs aiming at decreasing patient discomfort during administration period (e.g. prodrugs). Classified as highly toxic, they represent a major environmental problem that may potentiate disease occurrences. For newer cytostatics and pro-drugs there are no (or few) reported effects to aquatic organisms, which constraints their prioritization.

In face of the points raised, the IonCytDevice project intended to bridge some of these knowledge gaps and has delivered very important benchmarks. Predictions have been obtained on the environmental impacts of three cytostatics (cyclophosphamide: CYP; 5-fluoroucil: 5-FU; and mycophenolic acid: MPA) and one prodrug (capecitabine: CAP) on freshwater biota, with focus on new species and endpoints likely to be framed in meta-analysis studies as well. The results revealed that, for now, CYP, 5-FU, and CAP (prodrug) pose no risk, whilst MPA was flagged as of high environmental risk.

Keywords
antineoplastics
cancer
zebrafish
hydra
algae
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