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https://hdl.handle.net/11499/46364
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Sahin, Cigdem | - |
dc.contributor.author | Mutlu, Dogukan | - |
dc.contributor.author | Nasirli, Farid | - |
dc.contributor.author | Mahmoudi, Ghodrat | - |
dc.contributor.author | Zubkov, Fedor I. | - |
dc.contributor.author | Arslan, Sevki | - |
dc.contributor.author | Dogan, Nazime Mercan | - |
dc.date.accessioned | 2023-01-09T21:11:02Z | - |
dc.date.available | 2023-01-09T21:11:02Z | - |
dc.date.issued | 2021 | - |
dc.identifier.issn | 0966-0844 | - |
dc.identifier.issn | 1572-8773 | - |
dc.identifier.uri | https://doi.org/10.1007/s10534-021-00307-y | - |
dc.identifier.uri | https://hdl.handle.net/11499/46364 | - |
dc.description.abstract | This study represents synthesis, characterization, screening of antibiofilm efficacy, and cytotoxicity of iridium bis-terpyridine complexes. The complexes were characterized by NMR, MS, FTIR, UV/Visible, and fluorescence spectroscopies. The efficacy of biofilm inhibition and eradication of iridium complexes was evaluated using a crystal violet assay test and verified by fluorescence microscopy. Cytotoxicity and apoptosis analysis of iridium complexes were determined in this study. The results of our study revealed that three iridium complexes had the potential to inhibit biofilm formation and moderate the ability to destroy pre-formed biofilm of S. aureus ATCC 29,213. 250 mu M concentration of synthesized complexes showed the highest antibiofilm activity (75% for Ir1, 90% for Ir2, and 71% for Ir3). The significant inhibition obtained at 6.25 mu M concentration of Ir2 and Ir3 revealed the potential of our samples. Also, Ir1 and Ir2 complexes had a good capacity to destroy pre-formed biofilm. The results clearly showed that iridium complexes have cytotoxic activity towards colon cancer (Caco-2) and liver cancer (HepG2) cell lines without affecting non-cancerous cells (HEK293) at applied doses. Moreover, tested compounds induced apoptosis in these cancer cells. All of these results showed that iridium complexes had possessed the ability to inhibit or destroy pre-formed biofilm and could be developed as an effective agent against bacterial biofilms. Moreover, these pure substances may have valuable anti-cancer activity and it should be confirmed with further studies for therapeutic effects. | en_US |
dc.description.sponsorship | RUDN University Strategic Academic Leadership Program [PAU-BAP-2018-KRM-011, PAU-BAP-2020KRM005-016, PAU-BAP-2020KRM005-020] | en_US |
dc.description.sponsorship | S. A., C. S. and N. M. D. thank to Pamukkale University (PAU-BAP-2018-KRM-011 for the cytotoxicity and apoptosis studies, PAU-BAP-2020KRM005-016 for synthesis of iridium complexes, and PAU-BAP-2020KRM005-020 for antibiofilm studies). The synthesis of terpyridines ligands part of this paper has been supported by the RUDN University Strategic Academic Leadership Program. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Springer | en_US |
dc.relation.ispartof | Biometals | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Iridium complexes | en_US |
dc.subject | Terpyridine | en_US |
dc.subject | Antibiofilm | en_US |
dc.subject | Anticancer activity | en_US |
dc.subject | Photophysical Properties | en_US |
dc.subject | Cytotoxicity | en_US |
dc.subject | Resistance | en_US |
dc.subject | Tolerance | en_US |
dc.subject | Discovery | en_US |
dc.subject | Family | en_US |
dc.title | New iridium bis-terpyridine complexes: synthesis, characterization, antibiofilm and anticancer potentials | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 34 | en_US |
dc.identifier.issue | 3 | en_US |
dc.identifier.startpage | 701 | en_US |
dc.identifier.endpage | 713 | en_US |
dc.authorid | Mutlu, Dogukan/0000-0003-3259-5822 | - |
dc.authorid | Zubkov, Fedor I./0000-0002-0289-0831 | - |
dc.authorid | Mahmoudi, Ghodrat/0000-0002-4846-5283 | - |
dc.identifier.doi | 10.1007/s10534-021-00307-y | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.authorscopusid | 57202998424 | - |
dc.authorscopusid | 57212511655 | - |
dc.authorscopusid | 57223453976 | - |
dc.authorscopusid | 15765751200 | - |
dc.authorscopusid | 6603592191 | - |
dc.authorscopusid | 8684142100 | - |
dc.authorscopusid | 36117534100 | - |
dc.authorwosid | mahmoudi, ghodrat/AAB-6892-2022 | - |
dc.authorwosid | Mutlu, Dogukan/AAL-4976-2021 | - |
dc.authorwosid | Zubkov, Fedor I./A-6020-2012 | - |
dc.identifier.pmid | 33900533 | en_US |
dc.identifier.scopus | 2-s2.0-85105905543 | en_US |
dc.identifier.wos | WOS:000644277300003 | en_US |
dc.identifier.scopusquality | Q1 | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairetype | Article | - |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | 14.01. Surgical Medicine | - |
crisitem.author.dept | 17.02. Biology | - |
crisitem.author.dept | 17.02. Biology | - |
Appears in Collections: | Fen-Edebiyat Fakültesi Koleksiyonu PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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