Comparative Evaluation of the Inhibitory Potential of Synthetic N-Heterocycles, Cu/Fe3O4@SiO2 Nanocomposites and Some Natural Products against Non-Resistant and Antibiotic-Resistant Acinetobacter baumannii
Some thiazole derivatives were used to treat cancer, AIDS, blood lipids and hypertension diseases.19 Some synthesized thiazoles showed anti-inflammatory and antioxidant activities as well as blocking properties on anopheles mosquitoes or trypanosomes and fungi Candida albicans.20 Antimicrobial effec...
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Published in | Pharmaceutical Sciences Vol. 26; no. 2; pp. 184 - 192 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Tabriz
Tabriz University of Medical Sciences
01.06.2020
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Subjects | |
Online Access | Get full text |
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Summary: | Some thiazole derivatives were used to treat cancer, AIDS, blood lipids and hypertension diseases.19 Some synthesized thiazoles showed anti-inflammatory and antioxidant activities as well as blocking properties on anopheles mosquitoes or trypanosomes and fungi Candida albicans.20 Antimicrobial effects of thiazole derivatives were evaluated against a broad spectrum of bacterial pathogens such as Pseudomonas aeruginosa, Staphylococcus epidermidis and Bacillus subtilis.21 Imidazolidine ring is present in midazolam, phenytoin and ketoconazole that applied as anesthetic, anti-seizure and antifungal medicines.22-31 In addition, antibacterial effect of synthetic imidazolidines were assessed on S. aureus, Pseudomonas aeruginosa and E. coli.32,33 Antifungal, antimalarial, anticancer and anti-inflammatory activities were observed with compounds containing tetrahydropyrimidine core.34-38 Tetrahydropyrimidine derivatives could efficiently confront Pseudomonas aeruginosa and Klebsiella pneumoniae.39 To expand and discover new antimicrobial agents, inhibitory potentials of synthetic thiazole, imidazole and tetrahydropyrimidine derivatives, Cu/Fe3O4@ SiO2 nanocomposites, glycine, poly-L-lysine, nisin and hydroalcoholic extract of Trachyspermum ammi, Curcuma longa and green tea catechins were studied against nonresistant and antibiotic-resistant strains of A. baumannii. Extract was dissolved in 10% DMSO at initial concentrations of 10240 pg ml-1, and sterilized by 0.22 pm syringe filter.40 Preparation of Cu/Fe3O@SiO2 nanocomposites The Fe3O4 nanoparticles were prepared using electrochemical system as previously reported.41 A solution containing 0.90 g of copper chloride in 50 ml of aqueous ethanol 50% was added to a stirred mixture in an electrochemical cell including 0.27 g of Fe3O4@SiO2 in 50 ml of aqueous ethanol 50%. [...]the particles were separated using a magnet, washed with distillated water and calcined at 180 °C for 13 h to give Cu/Fe3O4@SiO2 nanocomposites.41 Synthesis of thiazoles 3a-f A mixture including 1 mmol of thioamide 1 (0.23 g,), 1-bromocarbonyl compounds 2a-f and sodium bicarbonate (0.08 g) in 1 ml DMF was stirred at ambient temperature (Figure 1). [...]the 0.5 McFarland turbidity standard of each bacterial strain was prepared in Mueller-Hinton broth (MHB) medium.44 Inhibition zone diameter (IZD) measurement 100 pl of bacterial suspension was spread on a plate 10 cm containing Mueller-Hinton agar (MHA). |
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ISSN: | 1735-403X 2383-2886 |
DOI: | 10.34172/PS.2020.12 |