Antimicrobial Activity of Water-Soluble Silver Complexes Bearing C-Scorpionate Ligands

The novel hydrosoluble silver coordination polymer [Ag(NO<sub>3</sub>)(μ-1κ<i>N</i>;2<i>κN</i>',<i>N</i>"-TPM<sup>OH</sup>)]<sub>n</sub> (<b>1</b>) (TPM<sup>OH</sup> = tris(1<i>H</i>...

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Main Authors: Abdallah G. Mahmoud (Author), Sílvia A. Sousa (Author), M. Fátima C. Guedes da Silva (Author), Luísa M. D. R. S. Martins (Author), Jorge H. Leitão (Author)
פורמט: ספר
יצא לאור: MDPI AG, 2024-07-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Abdallah G. Mahmoud  |e author 
700 1 0 |a Sílvia A. Sousa  |e author 
700 1 0 |a M. Fátima C. Guedes da Silva  |e author 
700 1 0 |a Luísa M. D. R. S. Martins  |e author 
700 1 0 |a Jorge H. Leitão  |e author 
245 0 0 |a Antimicrobial Activity of Water-Soluble Silver Complexes Bearing C-Scorpionate Ligands 
260 |b MDPI AG,   |c 2024-07-01T00:00:00Z. 
500 |a 10.3390/antibiotics13070647 
500 |a 2079-6382 
520 |a The novel hydrosoluble silver coordination polymer [Ag(NO<sub>3</sub>)(μ-1κ<i>N</i>;2<i>κN</i>',<i>N</i>"-TPM<sup>OH</sup>)]<sub>n</sub> (<b>1</b>) (TPM<sup>OH</sup> = tris(1<i>H</i>-pyrazol-1-yl)ethanol) was obtained and characterized. While single crystal X-ray diffraction analysis of compound <b>1</b> disclosed an infinite 1D helical chain structure in the solid state, NMR analysis in polar solvents confirmed the mononuclear nature of compound <b>1</b> in solution. Compound <b>1</b> and the analogue [Ag(μ-1κ<i>N</i>;2<i>κN</i>',<i>N</i>"-TPMS)]<sub>n</sub> (<b>2</b>) (TPMS = tris(1<i>H</i>-pyrazol-1-yl)methane sulfonate) were evaluated with regard to their antimicrobial activities towards the Gram-negative <i>Escherichia coli</i>, <i>Pseudomonas aeruginosa</i>, and <i>Burkholderia contaminans</i>, the Gram-positive <i>Staphylococcus aureus</i>, and the fungal species <i>Candida albicans</i> and <i>Candida glabrata</i>. Compound <b>1</b> exhibited minimal inhibitory concentration (MIC) values ranging from 2 to 7.7 µg/mL towards the tested Gram-negative bacteria, 18 µg/mL towards the Gram-positive <i>S. aureus</i>, and 15 and 31 µg/mL towards <i>C. albicans</i> and <i>C. glabrata</i>, respectively. Compound <b>2</b> was less effective towards the tested bacteria, with MIC values ranging from 15 to 19.6 µg/mL towards the Gram-negative bacteria and 51 µg/mL towards <i>S. aureus</i>; however, it was more effective against <i>C. albicans</i> and <i>C. glabrata</i>, with MIC values of about 6 µg/mL towards these fungal species. The toxicity of compounds <b>1</b> and <b>2</b> was assessed by evaluating the survival of the <i>Caenorhabditis elegans</i> model organism to concentrations of up to 100 µg/mL. The value of 50% lethality (LD<sub>50</sub>) could only be estimated as 73.2 µg/mL for compound <b>1</b> at 72 h, otherwise LD<sub>50</sub> was >100 µg/mL for both compounds <b>1</b> and <b>2</b>. These results indicate compounds <b>1</b> and <b>2</b> as novel silver complexes with interesting antimicrobial properties towards bacterial and fungal pathogens. 
546 |a EN 
690 |a silver 
690 |a complex 
690 |a water-soluble 
690 |a C-scorpionate 
690 |a antimicrobial 
690 |a antifungal 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antibiotics, Vol 13, Iss 7, p 647 (2024) 
787 0 |n https://www.mdpi.com/2079-6382/13/7/647 
787 0 |n https://doaj.org/toc/2079-6382 
856 4 1 |u https://doaj.org/article/3c674300161a47f9ad5de8ff67f01d2c  |z Connect to this object online.