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DC Field | Value | Language |
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dc.contributor.author | Talreja, Neetu | - |
dc.date.accessioned | 2023-05-22T06:53:12Z | - |
dc.date.available | 2023-05-22T06:53:12Z | - |
dc.date.issued | 2022-12-12 | - |
dc.identifier.uri | DOI https://doi.org/10.1039/D1NJ05931A | - |
dc.identifier.uri | http://gnanaganga.inflibnet.ac.in:8080/jspui/handle/123456789/695 | - |
dc.description.abstract | The emergence of bacterial resistance is increasing continuously due to the misuse of antibiotics that results in difficulty controlling the bacterial infection or the lack of treatment. Therefore, a new class of antibiotic or nano-antibiotic materials must be developed to treat bacterial infectious diseases. In this context, the present study focuses on synthesizing Cu-metal incorporated WS2 nanosheet (Cu–WS2-NS)-based antibiotic materials. The Cu–WS2-NS was synthesized via a liquid exfoliation process, followed by the incorporation of Cu-metal using a microwave process. The as-prepared WS2-NS and Cu–WS2-NS based antibiotics were characterized via SEM, EDS, and FT-IR analysis. The as-prepared WS2-NS and Cu–WS2-NS based antibiotic materials showed high biocompatibility or insignificant toxicity (∼0.78% and 3.7%) against erythrocyte cells, respectively. The as-prepared WS2-NS and Cu–WS2-NS based antibiotic materials effectively inhibited or killed (99.99%) both E. Coli and S. aureus bacterial strains. The antibacterial activity of the Cu–WS2-NS based antibiotic materials was mainly due to the Cu metal that binds with the sulfide group of WS2-NS. Interestingly, the Cu–WS2-NS-based antibiotic materials showed superior or comparable antibiotic ability to that of commercially available Ampicillin antibiotics. Therefore, the as-prepared Cu–WS2-NS based antibiotic materials might be potential emerging materials to treat infectious diseases or control bacterial infections. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.title | Synthesis of Cu-doped 2D-WS2 nanosheet-based nano-antibiotic materials for inhibiting E. Coli and S. aureus bacterial strains | en_US |
dc.type | Article | en_US |
Appears in Collections: | Journal Articles |
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