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Resistance Modulation Action, Time-Kill Kinetics Assay, and Inhibition of Biofilm Formation Effects of Plumbagin from Plumbago zeylanica Linn

机译:抗性调制作用,时间杀死动力学测定,抑制脂素Zeylanica Linn的肠球菌的抑制作用

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Antimicrobial resistance (AMR) is a threat to the prevention and treatment of the increasing range of infectious diseases. There is therefore the need for renewed efforts into antimicrobial discovery and development to combat the menace. The antimicrobial activity of plumbagin isolated from roots of Plumbago zeylanica against selected organisms was evaluated for resistance modulation antimicrobial assay, time-kill kinetics assay, and inhibition of biofilm formation. The minimum inhibitory concentrations (MICs) of plumbagin and standard drugs were determined via the broth microdilution method to be 0.5 to 8?μg/mL and 0.25–128?μg/mL, respectively. In the resistance modulation study, MICs of the standard drugs were redetermined in the presence of subinhibitory concentration of plumbagin (4?μg/mL), and plumbagin was found to either potentiate or reduce the activities of these standard drugs with the highest potentiation recorded up to 12-folds for ketoconazole against Candida albicans. Plumbagin was found to be bacteriostatic and fungistatic from the time-kill kinetics study. Plumbagin demonstrated strong inhibition of biofilm formation activity at concentrations of 128, 64, and 32?μg/mL against the test microorganisms compared with ciprofloxacin. Plumbagin has been proved through this study to be a suitable lead compound in antimicrobial resistance drug development.
机译:抗微生物耐药性(AMR)是对预防和治疗越来越多的传染病的威胁。因此,需要再次努力进行抗菌发现和发展,以打击威胁。评价从朱米达Zeylanica的根系与所选生物的抗菌活性进行抗菌活性,用于抗性调制抗菌测定,时间杀死动力学测定和生物膜形成的抑制作用。通过肉汤微量稀释方法测定肠球菌和标准药物的最小抑制浓度(MIC),分别测定为0.5至8Ω×mL和0.25-128Ω×mL。在抗性调制研究中,标准药物的麦克风在存在子宫内浓度(4ΩΩm1)的存在下,并发现肠果素与录制的最高潜力有关或减少这些标准药物的活性。对酮康唑对抗念珠菌蛋白糖苷的12倍。从时间杀死动力学研究中发现朱敏素是抑菌和真菌。与环丙沙星相比,肠果在128,64和32μg/ ml的浓度下表现出强烈的128,64和32μg/ ml的抑制。通过该研究证明了朱敏素是抗菌药物发育中合适的铅化合物。

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