The aim of this study was to determine the total phenolic content, evaluate antioxidant propertie and antimicrobial potential, and identify phenolic compounds in alcoholic and aqueous extracts of the wild cherry (Prunus avium L.) stems collected in Bosnia and Herzegovina. Alcoholic extracts had higher contents of phenolic and flavonoid components, as well as the antioxidant and ferric reducing antioxidant capacity in comparison to aqueous extracts. All extracts were characterized by HPLC analysis. Furthermore, for the first time, the antimicrobial properties of wild cherry stem extracts were evaluated. Quercetin and (+)-catechin were the main compounds identified in the alcoholic extract, followed by chlorogenic acid and rutin. Quercetin was also the major component detected in aqueous extracts. Besides, alcoholic extract showed better antibacterial properties against Staphylococcus aureus as a representative gram-positive bacteria than infusion, whereas none of the samples showed antibacterial activity against Escherichia coli and fungus Candida albicans.
In this work, four silver(I) complexes with Schiff bases derived from ninhydrin and selected amino acids (methionine, histidine, cysteine, and phenylalanine) were synthesized. The aim of this study is to determine the potential biological activity of these complexes. FTIR and UV/VIS spectroscopy were used for structural characterization of the products. Antioxidant activity was examined in vitro using DPPH method. Antimicrobial screening was performed by diffusion technique on reference bacterial strains from the ATCC collection. Interaction with bovine serum albumin (BSA) was examined using UV/VIS spectroscopy. Based on the obtained spectral data, it is assumed that all Schiff bases coordinate the Ag(I) ion as a tridentate ONO donor ligand. The antioxidant activity of the synthesized compounds is extremely high, with a range of IC50 values of 0.023-0.06 mg/mL. Antimicrobial screening determined the inhibitory ability of almost all complexes for concentrations of 1 and 2 mg/mL, with zones of inhibition in the range of 9-19 mm. Examination of the interaction of BSA with Ag(I) complexes revealed the same change in the absorption maximum (hyperchromic shift) in the region of about 205 nm, which indicates that the interaction of BSA and the complex results in conformational changes of BSA.
Ciprofloxacin, CFL is a drug that belongs to the second generation of fluoroquinolone antibiotics with a wide range of effects on Gram-positive and Gram-negative bacteria. The aim of this work was to investigate the interaction of CFL as ligand with divalent biological cations (Mn2+, Ni2+ and Co2+) in approximate physiological conditions. Synthesized complexes were characterized using FTIR and stereo-microscopy. Antimicrobial screening was performed on bacterial strains of Escherichia coli, Salmonella Enteritidis, Enterococcus faecalis and Staphylococcus aureus. The results of FTIR spectroscopy showed that the M(II) complexes with CFL were formed through the oxygen donors of the carboxyl and carbonyl group of the ligand. Stereo-microscopic characterization revealed the difference in color and size of crystals of the ligand and metal complexes. Antimicrobial screening has shown that CFL and complexes have almost similar antimicrobial activity against investigated bacterial strains.
Schiff bases are organic compounds formed by the reaction of the primary aminewith carbonyl compounds (aldehydes or ketones). These are mainly bi- or tridentateligands capable of forming very stable complexes with transitional metals. They areused as catalysts in oxygenation, hydrolysis, electro-reduction and decompositionreactions. Many Shiff bases show significant anti-tumor, antimicrobial and antifungalactivity, which are the subject of research by many scientists in the world.In this paper Schiff base from benzidine and 1,3-diphenyl-1,3-propanedione wassynthesized. To characterize the product, FTIR spectroscopy and stereo-microscopywere used. In order to determine biological activity, antibacterial, antifungal andantioxidant activity of the product was tested.The results showed that the interaction of benzidine and 1,3-diphenylpropanedioneresults in a Schiff base showing antibacterial, antifungal and antioxidant activity.
Deep eutectic solvents (DESs), as an alternative to ionic liquids, have greener credentials than ionic liquids and have attracted increasing attention in many applications. Choline chloride-based DESs in combination with different hydrogen bond donors (organic acid, sugars and urea), showed a high extraction efficiency. The aim of this study was to examine the possible effects of choline chloride-based eutectic solvents on the antioxidant and antimicrobial activity of lemon and mandarin orange seed extracts. Lactic acid, glucose, urea and water were used to prepare choline chloride-based Natural Deep Eutectic Solvents (NADESs). Ferric-Reducing Antioxidant Power (FRAP) Assay and 2,2-diphenyl-1-picryl-hydrazyl (DPPH) method were used to determine antioxidant activity. Antibacterial activity was investigated by diffusion method on reference bacterial strains E. coli, E. faecalis, S. aureus, B. subtilis and L. monocytogenes. The analysis revealed a significant reduction potential of the eutectic solvent based on lactic acid as well as significant antioxidant activity of lemon and mandarin seed extracts. In general, mandarin extracts showed better antioxidant capacity. In vitro antibacterial activity assays showed a complete absence of bacterial growth inhibition of the extracts. However, eutectic solvents with lactic acid have shown a significant antimicrobial effect.
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