Please use this identifier to cite or link to this item: https://doi.org/10.1002/bit.22363
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dc.titleAntioxidant and antibacterial activities of eugenol and carvacrol-grafted chitosan nanoparticles
dc.contributor.authorChen, F.
dc.contributor.authorShi, Z.
dc.contributor.authorNeoh, K.G.
dc.contributor.authorKang, E.T.
dc.date.accessioned2014-06-17T07:36:07Z
dc.date.available2014-06-17T07:36:07Z
dc.date.issued2009-09-01
dc.identifier.citationChen, F., Shi, Z., Neoh, K.G., Kang, E.T. (2009-09-01). Antioxidant and antibacterial activities of eugenol and carvacrol-grafted chitosan nanoparticles. Biotechnology and Bioengineering 104 (1) : 30-39. ScholarBank@NUS Repository. https://doi.org/10.1002/bit.22363
dc.identifier.issn00063592
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/63493
dc.description.abstractEssential oils are known to possess antimicrobial and antioxidant activity while chitosan is a biocompatible polymer with antibacterial activity against a broad spectrum of bacteria. In this work, nanoparticles with both antioxidant and antibacterial properties were prepared by grafting eugenol and carvacrol (two components of essential oils) on chitosan nanoparticles. Aldehyde groups were first introduced in eugenol and carvacrol, and the grafting of these oils to chitosan nanoparticles was carried out via the Schiff base reaction. The surface concentration of the grafted essential oil components was determined by X-ray photoelectron spectroscopy (XPS). The antioxidant activities of the carvacrol-grafted chitosan nanoparticles (CHCA NPs) and the eugenolgrafted chitosan nanoparticles (CHEU NPs) were assayed with diphenylpicrylhydrazyl (DPPH). Antibacterial assays were carried out with a representative gram-negative bacterium, Escherichia coli (E. coli) and a gram-positive bacterium, Staphylococcus aureus (S. aureus). The grafted eugenol and carvacrol conferred antioxidant activity to the chitosan nanoparticles, and the essential oil componentgrafted chitosan nanoparticles achieved an antibacterial activity equivalent to or better than that of the unmodified chitosan nanoparticles. Cytotoxicity assays using 3T3 mouse fibroblast showed that the cytotoxicity of CHEU NPs and CHCA NPs were significant lower than those of the pure essential oils. © 2009 Wiley Periodicals, Inc.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/bit.22363
dc.sourceScopus
dc.subjectAntibacterial
dc.subjectAntioxidant
dc.subjectCarvacrol
dc.subjectChitosan nanoparticles
dc.subjectEugenol
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1002/bit.22363
dc.description.sourcetitleBiotechnology and Bioengineering
dc.description.volume104
dc.description.issue1
dc.description.page30-39
dc.description.codenBIBIA
dc.identifier.isiut000269096800005
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