Evidence map›Paper›PMID 33900533›Full record

ArticleBiometals : an international journal on the role of metal ions in biology, biochemistry, and medicine2021

New iridium bis-terpyridine complexes: synthesis, characterization, antibiofilm and anticancer potentials.

Cigdem Sahin, Dogukan Mutlu, Farid Nasirli, Ghodrat Mahmoudi, Fedor I Zubkov, Sevki Arslan, Nazime Mercan Dogan

Abstract read
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Article in Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 16 citations in OpenAlex.

  1. Evaluation of the antifungal potential of N, N chelating iridium(III) complexes.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2026
    Article
  2. Article
  3. Inhibition and disruption of bacterial biofilms by a bipyridine-ruthenium complex: a broad-spectrum in vitro study.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2026
    Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 3 countries.

Cigdem SahinDepartment of Chemistry, Art & Science Faculty, Pamukkale University, 20160, Denizli, Turkey. cigdemsahin82@gmail.com.
Dogukan MutluDepartment of Biology, Art & Science Faculty, Pamukkale University, 20160, Denizli, Turkey.
Farid NasirliDepartment of Biology, Art & Science Faculty, Pamukkale University, 20160, Denizli, Turkey.
Ghodrat MahmoudiDepartment of Chemistry, Faculty of Science, University of Maragheh, P.O. Box 55181-83111, Maragheh, Iran. ghodratmahmoudi@gmail.com.
Fedor I ZubkovOrganic Chemistry Department, Faculty of Science, Peoples Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya Street, 117198, Moscow, Russian Federation.
Sevki ArslanDepartment of Biology, Art & Science Faculty, Pamukkale University, 20160, Denizli, Turkey. sevkia@pau.edu.tr.
Nazime Mercan DoganDepartment of Biology, Art & Science Faculty, Pamukkale University, 20160, Denizli, Turkey.
Pamukkale University · TRPeoples' Friendship University of Russia · RUUniversity of Maragheh · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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 µM 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 µM 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.

Indexed as

Anti-Bacterial AgentsAntineoplastic AgentsBiofilmsCell LineCell ProliferationCell SurvivalCoordination ComplexesDose-Response Relationship, DrugDrug Screening Assays, AntitumorHumansIridiumMicrobial Sensitivity TestsMolecular StructurePyridinesStaphylococcus aureusStructure-Activity RelationshipAnti-Bacterial AgentsAntineoplastic AgentsCoordination ComplexesIridiumPyridinesAntibiofilmAnticancer activityIridium complexesTerpyridine

Identifiers

PMID33900533
OpenAlexW3158028351

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.