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1.
Molecules ; 22(11)2017 Nov 07.
Article in English | MEDLINE | ID: mdl-29112179

ABSTRACT

A series of specific task ionic liquids (ILs) based on a pyridiniumhydrazone scaffold in combination with hexafluorophosphate (PF6-), tetrafluoroboron (BF4-) and/or trifluoroacetate (CF3COO-) counter anion, were designed and characterized by IR, NMR and mass spectrometry. The reactions were conducted under both conventional and green ultrasound procedures. The antifungal potential of the synthesized compounds 2-25 was investigated against 40 strains of Candida (four standard and 36 clinical isolates). Minimum inhibitory concentrations (MIC90) of the synthesized compounds were in the range of 62.5-2000 µg/mL for both standard and oral Candida isolates. MIC90 results showed that the synthesized 1-(2-(4-chlorophenyl)-2-oxoethyl)-4-(2-(4-fluorobenzylidene)hydrazinecarbonyl)-pyridin-1-ium hexafluorophosphate (11) was found to be most effective, followed by 4-(2-(4-fluorobenzylidene)hydrazinecarbonyl)-1-(2-(4-nitrophenyl)-2-oxoethyl)-pyridin-1-ium hexafluorophosphate (14) and 1-(2-ethoxy-2-oxoethyl)-4-(2-(4-fluorobenzylidene)hydrazinecarbonyl)pyridin-1-ium hexafluorophosphate (8). All the Candida isolates showed marked sensitivity towards the synthesized compounds. Ergosterol content was drastically reduced by more active synthesized compounds, and agreed well with MIC90 values. Confocal scanning laser microscopy (CLSM) results showed that the red colored fluorescent dye enters the test agent treated cells, which confirms cell wall and cell membrane damage. The microscopy results obtained suggested membrane-located targets for the action of these synthesized compounds. It appears that the test compounds might be interacting with ergosterol in the fungal cell membranes, decreasing the membrane ergosterol content and ultimately leading to membrane disruption as visible in confocal results. The present study indicates that these synthesized compounds show significant antifungal activity against Candida which forms the basis to carry out further in vivo experiments before their clinical use.


Subject(s)
Antifungal Agents/chemical synthesis , Green Chemistry Technology/methods , Hydrazones/chemical synthesis , Pyridinium Compounds/chemical synthesis , Antifungal Agents/chemistry , Antifungal Agents/pharmacology , Candida/drug effects , Hydrazones/chemistry , Hydrazones/pharmacology , Ionic Liquids/chemical synthesis , Ionic Liquids/chemistry , Ionic Liquids/pharmacology , Microbial Sensitivity Tests , Molecular Structure , Pyridinium Compounds/chemistry , Pyridinium Compounds/pharmacology
2.
Bioorg Med Chem ; 23(15): 4172-4180, 2015 Aug 01.
Article in English | MEDLINE | ID: mdl-26164624

ABSTRACT

A series of compounds in which 2-(4-ethyl-2-pyridyl)-1H-imidazole was clubbed with substituted 1,3,4-oxadiazole was synthesized and subjected to antifungal activity evaluation. In vitro assays indicated that several clubbed derivatives had excellent antifungal activity against different strains of laboratory and clinically isolated Candida species. Structural Activity Relationship (SAR) studies revealed that the presence and position of substituents on the phenyl ring of the 1,3,4-oxadiazole unit, guides the antifungal potential of the compounds, where compound 4b, 4c and 4g were found to be active against all the tested fungal strains. Impairment of ergosterol biosynthesis upon the concomitant treatment of 4b, 4c and 4g, revealed the possible mechanisms of antifungal action of these compounds. Inhibitors snugly fitting the active site of the target enzyme, as revealed by molecular docking studies, may well explain their excellent inhibitory activity.


Subject(s)
Antifungal Agents/chemistry , Antifungal Agents/pharmacology , Imidazoles/chemistry , Oxadiazoles/chemistry , Structure-Activity Relationship , Candida/drug effects , Candida/metabolism , Drug Evaluation, Preclinical/methods , Microbial Sensitivity Tests , Molecular Docking Simulation , Molecular Structure , Sterols/metabolism
3.
J Environ Sci (China) ; 31: 104-23, 2015 May 01.
Article in English | MEDLINE | ID: mdl-25968265

ABSTRACT

The direct determination of toxic metal ions, in environmental samples, is difficult because of the latter's presence in trace concentration in association with complex matrices, thereby leading to insufficient sensitivity and selectivity of the methods used. The simultaneous removal of the matrix and preconcentration of the metal ions, through solid phase extraction, serves as the promising solution. The mechanism involved in solid phase extraction (SPE) depends on the nature of the sorbent and analyte. Thus, SPE is carried out by means of adsorption, ion exchange, chelation, ion pair formation, and so forth. As polymeric supports, the commercially available Amberlite resins have been found very promising for designing chelating matrices due to its good physical and chemical properties such as porosity, high surface area, durability and purity. This review presents an overview of the various works done on the modification of Amberlite XAD resins with the objective of making it an efficient sorbent. The methods of modifications which are generally based on simple impregnation, sorption as chelates and chemical bonding have been discussed. The reported results, including the preconcentration limit, the detection limit, sorption capacity, preconcentration factors etc., have been reproduced.


Subject(s)
Metals/chemistry , Polystyrenes/chemistry , Polyvinyls/chemistry , Water Pollutants, Chemical/chemistry , Adsorption , Polymers/chemistry
5.
ScientificWorldJournal ; 2014: 404617, 2014.
Article in English | MEDLINE | ID: mdl-24772018

ABSTRACT

2-Phenyl-N,N'-bis(pyridin-4-ylcarbonyl)butanediamide ligand with a series of transition metal complexes has been synthesized via two routes: microwave irradiation and conventional heating method. Microwave irritation method happened to be the efficient and versatile route for the synthesis of these metal complexes. These complexes were found to have the general composition M(L)Cl2/M(L)(CH3COO)2 (where M = Cu(II), Co(II), Ni(II), and L = ligand). Different physical and spectroscopic techniques were used to investigate the structural features of the synthesized compounds, which supported an octahedral geometry for these complexes. In vitro antifungal activity of the ligand and its metal complexes revealed that the metal complexes are highly active compared to the standard drug. Metal complexes showed enhanced activity compared to the ligand, which is an important step towards the designing of antifungal drug candidates.


Subject(s)
Antifungal Agents/chemistry , Antifungal Agents/pharmacology , Coordination Complexes/chemistry , Coordination Complexes/pharmacology , Metals, Heavy/chemistry , Microwaves , Candida albicans/drug effects , Ligands , Microbial Sensitivity Tests , Molecular Structure
6.
Int J Nanomedicine ; 8: 3355-64, 2013.
Article in English | MEDLINE | ID: mdl-24039419

ABSTRACT

Nanotechnology is gaining momentum due to its ability to transform metals into nanoparticles. The synthesis, characterization, and applications of biologically synthesized nanomaterials have become an important branch of nanotechnology. Plant extracts are a cost-effective, ecologically friendly, and efficient alternative for the large-scale synthesis of nanoparticles. In this study, silver nanoparticles (AgNps) were synthesized using Rhinacanthus nasutus leaf extract. After exposing the silver ions to the leaf extract, the rapid reduction of silver ions led to the formation of AgNps in solution. The synthesis was confirmed by ultraviolet-visible spectroscopy, Fourier transform infrared spectroscopy, and transmission electron microscopy. The in vitro antimicrobial activity of the AgNps synthesized using R. nasutus leaf extract was investigated against Bacillus subtilis, Staphylococcus aureus, Pseudomonas aeruginosa, Klebsiella pneumonia, Escherichia coli, Aspergillus niger, and Aspergillus flavus using a disc diffusion method. The AgNps showed potential activity against all of the bacterial strains and fungal colonies, indicating that R. nasutus has the potential to be used in the development of value-added products in the biomedical and nanotechnology-based industries.


Subject(s)
Bacterial Physiological Phenomena/drug effects , Metal Nanoparticles/administration & dosage , Metal Nanoparticles/chemistry , Plant Extracts/chemistry , Plant Leaves/chemistry , Silver/chemistry , Acanthaceae , Anti-Infective Agents/chemical synthesis , Anti-Infective Agents/pharmacology , Apoptosis/drug effects , Biological Products/chemical synthesis , Biological Products/pharmacology , Cell Survival/drug effects , Materials Testing , Metal Nanoparticles/ultrastructure
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