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An inhibitory action of chitosan nanoparticles against pathogenic bacteria and fungi and their potential applications as biocompatible antioxidants.
- Source :
-
Microbial pathogenesis [Microb Pathog] 2018 Jan; Vol. 114, pp. 323-327. Date of Electronic Publication: 2017 Dec 08. - Publication Year :
- 2018
-
Abstract
- Chitosan is the second most abundant polymer obtained from the byproduct of seafood. Chitosan and its derivatives and chitosan loaded drugs are the recent area of interest against microbial pathogenesis. The cationic chitosan nanoparticles (ChNPs) interact with the anionic surfaces of the microbial cell membrane, which promotes antimicrobial activity. Although, ChNPs are potential against pathogenic microbes, selection of adaptable, suitable and cost effective synthesis method is much important. In the present study, ChNPs were synthesized adopting ionic gelation using sodium tripolyphosphate as a cross linking agent and characterized by FTIR, DLS, SEM and TEM analysis. ChNPs were investigated for antimicrobial activity against bacterial (Escherichia coli and Staphylococcus aureus) and fungal (Candida albicans) pathogens. ChNPs showed bactericidal activity at the lower minimum inhibitory concentration of about 40-80 μg mL <superscript>-1</superscript> . Interestingly, ChNPs exhibits biocompatible antioxidant property by inhibiting DPPH free radicals at 76% and also proven to be a potential candidate against the microbial pathogenesis with an inevitable applications in biomedicine.<br /> (Copyright © 2017 Elsevier Ltd. All rights reserved.)
- Subjects :
- Cell Survival drug effects
Chitosan chemistry
HeLa Cells drug effects
Humans
Microbial Sensitivity Tests
Nanotechnology
Particle Size
Anti-Infective Agents pharmacology
Antioxidants pharmacology
Bacteria drug effects
Biocompatible Materials pharmacology
Chitosan antagonists & inhibitors
Fungi drug effects
Nanoparticles chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1096-1208
- Volume :
- 114
- Database :
- MEDLINE
- Journal :
- Microbial pathogenesis
- Publication Type :
- Academic Journal
- Accession number :
- 29229504
- Full Text :
- https://doi.org/10.1016/j.micpath.2017.11.043