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Cited by 191

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

High Antibacterial Activity of Functionalized Chemically Exfoliated MoS2

Pandit, Subhendu, Karunakaran, Subbaraj, Boda, Sunil Kumar, Basu, Bikramjit, De, Mrinmoy·2016·ACS Applied Materials & Interfaces

Abstract

In view of the implications of inherent resistance of pathogenic bacteria, especially ESKAPE pathogens toward most of the commercially available antibiotics and the importance of these bacteria-induced biofilm formation leading to chronic infection, it is important to develop new-generation synthetic materials with greater efficacy toward antibacterial property. In addressing this issue, this paper reports a proof-of-principle study to evaluate the potential of functionalized two-dimensional chemically exfoliated MoS 2 (ce-MoS 2 ) toward inhibitory and bactericidal property against two representative ESKAPE pathogenic strain—a Gram-positive Staphylococcus aureus (MRSA) and a Gram-negative Pseudomonas aeruginosa . More significantly, the mechanistic study establishes a different extent of oxidative stress together with rapid membrane depolarization in contact with ce-MoS 2 having ligands of varied charge and hydrophobicity. The implication of our results is discussed in the light of the lack of survivability of planktonic bacteria and biofilm destruction in vitro. A comparison with widely used small molecules and other nanomaterial-based therapeutics conclusively establishes a better efficacy of 2D ce-MoS 2 as a new class of antibiotics.

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Crossref · 10.1021/acsami.6b10916

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Metadata

Authors
Pandit, S., Karunakaran, S., Boda, S. K., Basu, B., & De, M.
Venue
ACS Applied Materials & Interfaces
Published
2016-11-08
Volume
8
Issue
46
Pages
31567-31573
ISSN
  • 1944-8244 (ISSN-L)
  • 1944-8252
OpenAlex
W2539567878
Cited by
191
References
2
FWCI
6.98
Type
journal article
Language
en
Open access
closed

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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