izpis_h1_title_alt

Clinically used antifungal azoles as ligands for gold(III) complexes : the influence of the Au(III) ion on the antimicrobial activity of the complex
ID Stevanović, Nevena Lj. (Avtor), ID Kljun, Jakob (Avtor), ID Aleksić, Ivana (Avtor), ID Skaro-Bogojevic, Sanja (Avtor), ID Milivojević, Dušan (Avtor), ID Veselinovic, Aleksandar (Avtor), ID Turel, Iztok (Avtor), ID Djuran, Miloš I. (Avtor), ID Nikodinović-Runić, Jasmina (Avtor), ID Glišić, Biljana Đ. (Avtor)

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Izvleček
In a search for novel antimicrobial metal-based therapeutic agents, mononuclear gold(III) complexes 1–7 of the general formula [AuCl$_3$(azole)], where azole stands for imidazole (im, 1), 1-isopropylimidazole (ipim, 2), 1-phenylimidazole (phim, 3), clotrimazole (ctz, 4), econazole (ecz, 5), tioconazole (tcz, 6) and voriconazole (vcz, 7) were synthesized, characterized and biologically evaluated. In all complexes, the corresponding azole ligand is monodentately coordinated to the Au(III) via the imidazole or triazole nitrogen atom, while the remaining coordination sites are occupied by chloride anions leading to the square-planar arrangement. In vitro antimicrobial assays showed that the complexation of inactive azoles, imidazole, 1-isopropylimidazole and 1-phenylimidazole, to the Au(III) ion led to complexes 1–3, respectively, with moderate activity against the investigated strains and low cytotoxicity on the human normal lung fibroblast cell line (MRC-5). Moreover, gold(III) complexes 4–7 with clinically used antifungal agents clotrimazole, econazole, tioconazole and voriconazole, respectively, have, in most cases, enhanced antimicrobial effectiveness relative to the corresponding azoles, with the best improvement achieved after complexation of tioconazole (6) and voriconazole (7). The complexes 4–7 and the corresponding antifungal azoles inhibited the growth of dermatophyte Microsporum canis at 50 and 25 μg mL$^{−1}$. Gold(III) complexes 1–3 significantly reduced the amount of ergosterol in the cell membrane of Candida albicans at the subinhibitory concentration of 0.5 × MIC (minimal inhibitory concentration), while the corresponding imidazole ligands did not significantly affect the ergosterol content, indicating that the mechanism of action of the gold(III)–azole complexes is associated with inhibition of ergosterol biosynthesis. Finally, complexes 5 and 6 significantly reduced the production of pyocyanin, a virulence factor in Pseudomonas aeruginosa controlled by quorum sensing, and increased cell survival after exposure to this bacterium. These findings could be of importance for the development of novel gold(III)-based antivirulence therapeutic agents that attenuate virulence without pronounced effect on the growth of the pathogens, offering a lower risk for resistance development.

Jezik:Angleški jezik
Vrsta gradiva:Članek v reviji
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:FKKT - Fakulteta za kemijo in kemijsko tehnologijo
Status publikacije:Objavljeno
Različica publikacije:Objavljena publikacija
Leto izida:2022
Št. strani:Str. 5322-5334
Številčenje:Vol. 51, iss. 13
PID:20.500.12556/RUL-141872 Povezava se odpre v novem oknu
UDK:546.593:547.78
ISSN pri članku:1477-9234
DOI:10.1039/D2DT00411A Povezava se odpre v novem oknu
COBISS.SI-ID:102922499 Povezava se odpre v novem oknu
Datum objave v RUL:10.10.2022
Število ogledov:594
Število prenosov:89
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Dalton transactions
Skrajšan naslov:Dalton trans
Založnik:Royal Society of Chemistry
ISSN:1477-9234
COBISS.SI-ID:519833113 Povezava se odpre v novem oknu

Licence

Licenca:CC BY-NC 3.0, Creative Commons Priznanje avtorstva-Nekomercialno 3.0 Nedoločena
Povezava:https://creativecommons.org/licenses/by-nc/3.0/deed.sl
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Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:organokovinski kompleksi, zlato, azoli, protimikrobno delovanje

Projekti

Financer:MESTD - Ministry of Education, Science and Technological Development of Republic of Serbia
Številka projekta:451-03-68/2022-14/200042

Financer:MESTD - Ministry of Education, Science and Technological Development of Republic of Serbia
Številka projekta:451-03-68/2022-14/200122

Financer:ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:P1-0175
Naslov:Napredna anorganska kemija

Financer:Drugi - Drug financer ali več financerjev
Program financ.:Serbian Academy of Sciences and Arts, Strategic projects programme
Številka projekta:01-2019-F65

Financer:Drugi - Drug financer ali več financerjev
Program financ.:Serbian Academy of Sciences and Arts
Številka projekta:F128

Financer:Drugi - Drug financer ali več financerjev
Program financ.:Republic of Slovenia, Ministry of Education, Science and Sport, CMEPIUS, Mobility Grant

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