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Nanobased Antibacterial Drug Discovery to Treat Skin Infections O Using -Assisted Zinc Oxide Nanoparticle and Molecular Simulation Study

Overview
Journal Biomed Res Int
Publisher Wiley
Date 2022 Feb 21
PMID 35187170
Authors
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Abstract

In addition to the physical barrier, the epidermis acts as a natural barrier against microbial proliferation. It is prone to bacterial infections on the skin and in the nose, such as Staphylococcus aureus, as well as a variety of other skin illnesses. Green nanomaterial production, which eliminates the use of harmful chemicals while simultaneously reducing time, is gaining popularity in the nanotechnology area. Using the leaf extract of the pharmacologically valuable plant Moringa oleifera, we described a green synthesis of ZnO NPs (zinc oxide nanoparticles). ZnO NPs had a particle size of 201.6 nm and a zeta potential of -56.80 mV, respectively. A novel aminoketone antibacterial medication was synthesized and tested for antibacterial activity using ZnO NPs as a phytocatalyst in this work. This method produces high yields while maintaining efficient and gentle reaction conditions. Moringa oleifera extract can reduce ZnO to ZnO NPs in a straightforward manner. FT-IR, H-NMR, C-NMR, mass spectra, elemental analysis, and morphological analysis were used to synthesize and describe the antibacterial medicines (1a-1g) and (2a-2g). In addition, antibacterial activity was evaluated against bacteria such as and and compound 1c (63 g/mL, ) and compound 2e (0.12 g/mL, ) were found to be very active when compared to other medications. mupirocin is used as a reference. In addition, studies of in silico molecular docking for the bacterial DsbA protein were conducted. The strong molecules 1c (-4.3 kcal/mol) and 2e (-5.1 kcal/mol) exhibit a high binding affinity through hydrogen bonding, according to docking tests.

Citing Articles

Retracted: Nanobased Antibacterial Drug Discovery to Treat Skin Infections of Using -Assisted Zinc Oxide Nanoparticle and Molecular Simulation Study.

International B Biomed Res Int. 2024; 2024:9894601.

PMID: 38230154 PMC: 10791312. DOI: 10.1155/2024/9894601.

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