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Copper(II) and zinc(II) complexes with the clinically used fluconazole : comparison of antifungal activity and therapeutic potential
ID Stevanović, Nevena Lj. (Avtor), ID Aleksić, Ivana (Avtor), ID Kljun, Jakob (Avtor), ID Skaro-Bogojevic, Sanja (Avtor), ID Veselinovic, Aleksandar (Avtor), ID Nikodinović-Runić, Jasmina (Avtor), ID Turel, Iztok (Avtor), ID Djuran, Miloš I. (Avtor), ID Glišić, Biljana Đ. (Avtor)

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Izvleček
Copper(II) and zinc(II) complexes with clinically used antifungal drug fluconazole (fcz), {[CuCl$_2$(fcz)$_2$]·5H$_2$O}$_n$, 1, and {[ZnCl$_2$(fcz)$_2$]·2C$_2$H$_5$OH}$_n$, 2, were prepared and characterized by spectroscopic and crystallographic methods. The polymeric structure of the complexes comprises four fluconazole molecules monodentately coordinated via the triazole nitrogen and two chlorido ligands. With respect to fluconazole, complex 2 showed significantly higher antifungal activity against Candida krusei and Candida parapsilosis. All tested compounds reduced the total amount of ergosterol at subinhibitory concentrations, indicating that the mode of activity of fluconazole was retained within the complexes, which was corroborated via molecular docking with cytochrome P450 sterol 14α-demethylase (CYP51) as a target. Electrostatic, steric and internal energy interactions between the complexes and enzyme showed that 2 has higher binding potency to this target. Both complexes showed strong inhibition of C. albicans filamentation and biofilm formation at subinhibitory concentrations, with 2 being able to reduce the adherence of C. albicans to A549 cells in vitro. Complex 2 was able to reduce pyocyanin production in Pseudomonas aeruginosa between 10% and 25% and to inhibit its biofilm formation by 20% in comparison to the untreated control. These results suggest that complex 2 may be further examined in the mixed Candida-P. aeruginosa infections.

Jezik:Angleški jezik
Ključne besede:copper(II) complex, zinc(II) complex, fluconazole, antifungal agents, anti-biofilm activity
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:2021
Št. strani:20 str.
Številčenje:Vol. 14, iss. 1, art. 24
PID:20.500.12556/RUL-134922 Povezava se odpre v novem oknu
UDK:546.47:546.562
ISSN pri članku:1424-8247
DOI:10.3390/ph14010024 Povezava se odpre v novem oknu
COBISS.SI-ID:45141251 Povezava se odpre v novem oknu
Datum objave v RUL:11.02.2022
Število ogledov:941
Število prenosov:130
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Pharmaceuticals
Skrajšan naslov:Pharmaceuticals
Založnik:MDPI
ISSN:1424-8247
COBISS.SI-ID:517582617 Povezava se odpre v novem oknu

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Začetek licenciranja:01.01.2021

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:baker, cink, kovinski kompleksi

Projekti

Financer:MESTD - Ministry of Education, Science and Technological Development of Republic of Serbia
Številka projekta:451-03-68/2020-14/200042

Financer:MESTD - Ministry of Education, Science and Technological Development of Republic of Serbia
Številka projekta:451-03-68/2020-14/200122

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
Številka projekta:01-2019-F65

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

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