1.Antibacterial and Pharmacological Evaluation of Fluoroquinolones: A Chemoinformatics Approach.
Damini SOOD ; Neeraj KUMAR ; Aarushi SINGH ; Meena Kishore SAKHARKAR ; Vartika TOMAR ; Ramesh CHANDRA
Genomics & Informatics 2018;16(3):44-51
Fluoroquinolone (FQ) antibiotics are an important class of synthetic antibacterial agents. These are the most extensively used drugs for treating bacterial infections in the field of both human and veterinary medicine. Herein, the antibacterial and pharmacological properties of four fluoroquinolones: lomefloxacin, norfloxacin, ciprofloxacin, and ofloxacin have been studied. The objective of this study was to analyze the antibacterial characteristics of the different fluoroquinolones. Also, the pharmacological properties of the compounds including the Lipinski rule of five, absorption, distribution, metabolism, and excretion, LD50, drug likeliness, and toxicity were evaluated. We found that among all four FQ molecules, ofloxacin showed the highest antibacterial activity through in silico assays with a strong interaction (−38.52 kJ/mol) with the antibacterial target protein (topoisomerase-II DNA gyrase enzyme). The pharmacological and pharmacokinetic analysis also showed that the compounds ciprofloxacin, ofloxacin, lomefloxacin and norfloxacin have good pharmacological properties. Notably, ofloxacin was found to possess an IGC50 (concentration needed to inhibit 50% growth) value of 0.286 μg/L against the Tetrahymena pyriformis protozoa. It also tested negative for the Ames toxicity test, showing its non-carcinogenic character.
Absorption
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Anti-Bacterial Agents
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Bacterial Infections
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Ciprofloxacin
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Computer Simulation
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DNA Gyrase
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Fluoroquinolones*
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Humans
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Lethal Dose 50
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Metabolism
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Norfloxacin
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Ofloxacin
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Tetrahymena pyriformis
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Toxicity Tests
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Veterinary Medicine
2.In vitro toxicity of melamine against Tetrahymena pyriformis cells.
Zhengfang WANG ; Liben CHEN ; Rashad AL-KASIR ; Bo HAN
Journal of Veterinary Science 2011;12(1):27-34
This study assessed the toxicity of melamine against the unicellular eukaryotic system of Tetrahymena (T.) pyriformis exposed to 0, 0.05, 0.25, 0.5, 2.5, and 5 mg/mL of melamine. Cell growth curves of different cultures, the half maximum inhibition concentration (IC50) value of melamine, and morphological changes in cells were obtained via optical and transmission electron microscopic observation. The effects of eleven melamine concentrations, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5 and 5 mg/mL, on protein expression levels of T. pyriformis were examined using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). The results showed an obvious inhibitory effect of melamine on the growth of eukaryotic cells. Cell growth dynamics indicated that the IC50 value of melamine on T. pyriformis was 0.82 mg/mL. The cellular morphology was also affected in a concentration-dependent manner, with characteristics of atrophy or cell damage developing in the presence of melamine. The relative contents of the top four main proteins corresponding to peak mass-to-charge ratios (m/z) of 4466, m/z 6455, m/z 6514, and m/z 7772 in the MALDI-TOF-MS spectra were all found to be closely correlated with the melamine concentrations. In conclusion, exposure of eukaryotic cells to melamine could inhibit cell growth, cause changes in cytomorphology and even disturb the expression of proteins in a concentration-dependent manner. The described method of examining four sensitive proteins affected by melamine was also proposed to be used in a preliminary study to identify protein biomarkers in T. pyriformis.
Animal Feed/analysis/toxicity
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Biological Markers/analysis
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Food Additives/analysis/toxicity
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Inhibitory Concentration 50
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Microscopy, Electron, Transmission
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Protozoan Proteins/analysis
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Spectrometry, Mass, Matrix-Assisted Laser De
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Tetrahymena pyriformis/cytology/*drug effects
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Triazines/*toxicity