kth.sePublications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Oxidative, Genotoxic and Cytotoxic Damage Potential of Novel Borenium and Borinium Compounds
Department of Medical Services and Techniques, Vocational School of Health Services, University of Gaziantep, Gaziantep, 27410, Turkey.
Department of Medical Biology, Faculty of Medicine, Atatürk University, Erzurum 25040, Turkey;.
Department of Chemistry, Arts and Science Faculty, Düzce University, Düzce, 81620, Turkey.
Department of Otorhinolaryngology Diseases, Faculty of Medicine, Atatürk University, Erzurum 25040, Turkey;.
Show others and affiliations
2023 (English)In: Inorganics, E-ISSN 2304-6740, Vol. 11, no 8, article id 324Article in journal (Refereed) Published
Abstract [en]

In this study, the biological properties of novel borenium and borinium compounds in terms of their oxidative, genotoxic, and cytotoxic effects were assessed on cultured human peripheral blood cells, as well as several types of cancer cells. Our results revealed that the borinium compounds yielded the best results in terms of supporting total antioxidant capacity (TAC). In fact, borenium 1, borenium 2, borenium 3, borinium 4, and borinium 5 compounds elevated TAC levels of cultured human blood cells at rates of 42.8%, 101.5%, 69.8%, 33.3%, and 49.2%, respectively. There were no statistically significant differences (p > 0.05) between the negative control and the groups treated with all borinium and borenium concentrations from the micronucleus (MN) and chromosome aberration (CA) assays, demonstrating the non-genotoxic effects. Moreover, borenium 1 (60.7% and 50.7%), borenium 2 (70.4% and 57.2%), borenium 3 (53.1% and 45.2%), borinium 4 (55.1% and 48.1%), and borinium 5 (51.0% and 36.1%) minimized the mitomycin C(MMC)-induced genotoxic damages at different rates as determined using CA and MN assays, respectively. Again, it was found that the borinium compounds exhibited higher cytotoxic activity on cancer cells when compared to borenium compounds. Consequently, in light of our in vitro findings, it was suggested that the novel borinium and borenium compounds could be used safely in pharmacology, cosmetics, and various medical fields due to their antioxidant and non-genotoxic features, as well as their cytotoxicity potential on cancer cells.

Place, publisher, year, edition, pages
MDPI AG , 2023. Vol. 11, no 8, article id 324
Keywords [en]
antigenotoxicity, antioxidant, borenium, borinium, boron compounds, cancer cells, cytotoxicity, genotoxicity, human blood cells
National Category
Pharmacology and Toxicology
Identifiers
URN: urn:nbn:se:kth:diva-336566DOI: 10.3390/inorganics11080324ISI: 001056218200001Scopus ID: 2-s2.0-85169054736OAI: oai:DiVA.org:kth-336566DiVA, id: diva2:1798012
Note

QC 20230918

Available from: 2023-09-18 Created: 2023-09-18 Last updated: 2023-09-22Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textScopus

Authority records

Mardinoglu, Adil

Search in DiVA

By author/editor
Mardinoglu, Adil
By organisation
Science for Life Laboratory, SciLifeLabSystems Biology
Pharmacology and Toxicology

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 35 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf