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Zinc Oxide Nanoparticles Promise Anticancer and Antibacterial Activity in Ovarian Cancer

BACKGROUND: Ovarian cancer is the most lethal cancer in gynaecology. Surgery, chemotherapy, and radiotherapy are the most often used cancer-fighting strategies. Post-surgery infection is fairly prevalent, especially among people with insufficient immunity. Zinc oxide nanoparticles (ZnOnps) have amaz...

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Autores principales: Mousa, Ahmed Bakr, Moawad, Raghda, Abdallah, Yasmine, Abdel-Rasheed, Mazen, Zaher, Azza M. Abdel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072921/
https://www.ncbi.nlm.nih.gov/pubmed/37016170
http://dx.doi.org/10.1007/s11095-023-03505-0
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author Mousa, Ahmed Bakr
Moawad, Raghda
Abdallah, Yasmine
Abdel-Rasheed, Mazen
Zaher, Azza M. Abdel
author_facet Mousa, Ahmed Bakr
Moawad, Raghda
Abdallah, Yasmine
Abdel-Rasheed, Mazen
Zaher, Azza M. Abdel
author_sort Mousa, Ahmed Bakr
collection PubMed
description BACKGROUND: Ovarian cancer is the most lethal cancer in gynaecology. Surgery, chemotherapy, and radiotherapy are the most often used cancer-fighting strategies. Post-surgery infection is fairly prevalent, especially among people with insufficient immunity. Zinc oxide nanoparticles (ZnOnps) have amazing biomedical features as anticancer and antibacterial agents. METHODS: We investigated the behaviour of ZnOnps synthesized by green methods on ovarian cancers using established human ovarian cancer cell lines, besides the antibacterial action toward models of gram + ve and gram -ve bacteria. The cytotoxic effect of ZnOnps was calculated using a Sulforhodamine B (SRB) trial. Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) were tested as models for gram + ve and gram -ve bacteria. The selected bacteria were subjected to concentrations of 20, 40, 80, and 100 μg/ml. RESULTS: The synthesized ZnOnps induced 50% inhibitory concentration (IC50) at a concentration of 27.45 μg/ml. The diameter of inhibition ranged between 20.16 ± 0.16 and 27 ± 0.57 mm for S. aureus and 25.66 ± 0.33 to 31 ± 0.33 mm for E. coli. ZnOnps antagonistic effect statistically differed with neomycin, cefaclor, and cefadroxil. CONCLUSIONS: Green synthesis of ZnOnps is easily prepared, low cost, non-toxic, and eco-friendly. Their cytotoxic action on SKOV3 cells and their antibacterial characteristics pave the way to be an alternative therapy for ovarian cancer and S. aureus and E. coli infection.
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spelling pubmed-100729212023-04-04 Zinc Oxide Nanoparticles Promise Anticancer and Antibacterial Activity in Ovarian Cancer Mousa, Ahmed Bakr Moawad, Raghda Abdallah, Yasmine Abdel-Rasheed, Mazen Zaher, Azza M. Abdel Pharm Res Original Research Article BACKGROUND: Ovarian cancer is the most lethal cancer in gynaecology. Surgery, chemotherapy, and radiotherapy are the most often used cancer-fighting strategies. Post-surgery infection is fairly prevalent, especially among people with insufficient immunity. Zinc oxide nanoparticles (ZnOnps) have amazing biomedical features as anticancer and antibacterial agents. METHODS: We investigated the behaviour of ZnOnps synthesized by green methods on ovarian cancers using established human ovarian cancer cell lines, besides the antibacterial action toward models of gram + ve and gram -ve bacteria. The cytotoxic effect of ZnOnps was calculated using a Sulforhodamine B (SRB) trial. Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) were tested as models for gram + ve and gram -ve bacteria. The selected bacteria were subjected to concentrations of 20, 40, 80, and 100 μg/ml. RESULTS: The synthesized ZnOnps induced 50% inhibitory concentration (IC50) at a concentration of 27.45 μg/ml. The diameter of inhibition ranged between 20.16 ± 0.16 and 27 ± 0.57 mm for S. aureus and 25.66 ± 0.33 to 31 ± 0.33 mm for E. coli. ZnOnps antagonistic effect statistically differed with neomycin, cefaclor, and cefadroxil. CONCLUSIONS: Green synthesis of ZnOnps is easily prepared, low cost, non-toxic, and eco-friendly. Their cytotoxic action on SKOV3 cells and their antibacterial characteristics pave the way to be an alternative therapy for ovarian cancer and S. aureus and E. coli infection. Springer US 2023-04-04 2023 /pmc/articles/PMC10072921/ /pubmed/37016170 http://dx.doi.org/10.1007/s11095-023-03505-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Research Article
Mousa, Ahmed Bakr
Moawad, Raghda
Abdallah, Yasmine
Abdel-Rasheed, Mazen
Zaher, Azza M. Abdel
Zinc Oxide Nanoparticles Promise Anticancer and Antibacterial Activity in Ovarian Cancer
title Zinc Oxide Nanoparticles Promise Anticancer and Antibacterial Activity in Ovarian Cancer
title_full Zinc Oxide Nanoparticles Promise Anticancer and Antibacterial Activity in Ovarian Cancer
title_fullStr Zinc Oxide Nanoparticles Promise Anticancer and Antibacterial Activity in Ovarian Cancer
title_full_unstemmed Zinc Oxide Nanoparticles Promise Anticancer and Antibacterial Activity in Ovarian Cancer
title_short Zinc Oxide Nanoparticles Promise Anticancer and Antibacterial Activity in Ovarian Cancer
title_sort zinc oxide nanoparticles promise anticancer and antibacterial activity in ovarian cancer
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10072921/
https://www.ncbi.nlm.nih.gov/pubmed/37016170
http://dx.doi.org/10.1007/s11095-023-03505-0
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