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Tailoring copper(II) complexes with pyridine-4,5-dicarboxylate esters for anti-Candida activity
ID Andrejević, Tina P. (Avtor), ID Aleksić, Ivana (Avtor), ID Počkaj, Marta (Avtor), ID Kljun, Jakob (Avtor), ID Milivojević, Dušan (Avtor), ID Stevanović, Nevena Lj. (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
Five novel copper(II) complexes with pyridine-4,5-dicarboxylate esters as ligands, [Cu(NO$_3$)(py-2tz)(H$_2$O)$_3$]NO$_3$ (1), [Cu(NO$_3$)$_2$(py-2metz)(H$_2$O)] (2), [Cu(NO$_3$)$_2$(py-2py)(H$_2$O)]·H$_2$O (3), [CuCl$_2$(py-2tz)]$_2$ (4) and [CuCl$_2$(py-2metz)]$_n$ (5) (py-2tz is dimethyl 2-(thiazol-2-yl)pyridine-4,5-dicarboxylate, py-2metz is dimethyl 2-(4-methylthiazol-2-yl)pyridine-4,5-dicarboxylate and py-2py is dimethyl 2,2’-bipyridine-4,5-dicarboxylate), were synthesized and structurally characterized by different spectroscopic and electrochemical methods. The structure of these complexes was determined by single-crystal X-ray diffraction analysis, confirming the bidentate coordination mode of the corresponding pyridine-4,5-dicarboxylate ester to the Cu(II) ion through the nitrogen atoms. The antimicrobial potential of copper(II) complexes 1–5 was assessed against two bacterial and two Candida species. These complexes showed better growth inhibiting activity against Candida spp. with respect to the tested bacterial species, also being moderately toxic towards normal human lung fibroblast cells (MRC-5). Complexes 1 and 4 showed the greatest ability to inhibit the filamentation of C. albicans, which is an important process during fungal infection, and these two complexes efficiently inhibited the biofilm formation of C. albicans at subinhibitory concentrations. Complex 4 also successfully prevented the adhesion of C. albicans in an in vitro epithelial cell model. The mechanism of the antifungal activity of copper(II) complexes 1–5 was studied through their interaction with ct-DNA, as one of the possible target biomolecules, by fluorescence spectroscopy and gel electrophoresis. Finally, the ability of these complexes to bind to bovine serum albumin (BSA) was studied by fluorescence emission spectroscopy.

Jezik:Angleški jezik
Ključne besede:copper(II) complexes, pyridine-4, 5-dicarboxylates, antimicrobial activity, Candida albicans, filamentation, DNA/BSA interaction
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:Str. 2627-2638
Številčenje:Vol. 50, iss. 7
PID:20.500.12556/RUL-141863 Povezava se odpre v novem oknu
UDK:546.562:547.82
ISSN pri članku:1477-9234
DOI:10.1039/D0DT04061D Povezava se odpre v novem oknu
COBISS.SI-ID:50313731 Povezava se odpre v novem oknu
Datum objave v RUL:10.10.2022
Število ogledov:407
Število prenosov:83
Metapodatki:XML RDF-CHPDL 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 3.0, Creative Commons Priznanje avtorstva 3.0 Nedoločena
Povezava:https://creativecommons.org/licenses/by/3.0/deed.sl
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Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:bakrovi(II) kompleksi, piridin-4, 5-dikarboksilati, protimikrobna aktivnost, Candida albicans, filamentacija, DNA/BSA interakcija

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, 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

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