Antibacterial and Anticandidal Activity of the Nanostructural Composite of a Spirothiazolidine-Derivative Assembled on Silver Nanoparticles

Our aims in this work are the preparation of an ionic liquid based on heterocyclic compounds with Ag nanoparticles and the investigation of its application as an antibacterial and anticandidal agent. These goals were achieved through the fabrication of an ionic liquid based on Ag nanoparticles with...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2024-03, Vol.29 (5), p.1139
Hauptverfasser: Alshammari, Odeh A O, Azzam, Eid M S, Alhar, Munirah S, Alanazi, Kaseb D, Aljuhani, Sara A A, Elsofany, Walaa I
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Sprache:eng
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Zusammenfassung:Our aims in this work are the preparation of an ionic liquid based on heterocyclic compounds with Ag nanoparticles and the investigation of its application as an antibacterial and anticandidal agent. These goals were achieved through the fabrication of an ionic liquid based on Ag nanoparticles with 5-Amino-3-(4-fluorophenyl)-N-hexadecyl-7-(4-methylphenyl)-2-H spiro[cyclohexane1,2'-[1,3]thiazolo [4,5-b]pyridine]-6-carbonitrile ( ). The nanostructure of the prepared ionic liquid was characterized using techniques such as FTIR, HNMR, CNMR, UV, SEM, and TEM. The biological activity of the prepared compound ( ) and its nanocomposites with Ag nanoparticles was tested using five clinical bacteria ( 249; 141; cloacae 235; BC 161, and methicillin-resistant 217), and three Candida species ( ATCC 9255; ATCC 1362, and ATCC 20402). The FTIR, HNMR, and CNMR results confirmed the chemical structure of the synthesized compound. The nanostructure of the prepared ionic liquid was determined based on data obtained from the UV, SEM, and TEM tests. The antibacterial and anticandidal results showed that the biological activity of the compound ( ) was enhanced after the formation of nanocomposite structures with Ag nanoparticles. Moreover, the biological activity of the compound itself ( ) and that of its nanocomposite structure with Ag nanoparticles was higher than that of ampicillin and amphotericin B, which were used as control drugs in this work.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules29051139