Covalent assembly of metal nanoparticles on cellulose fabric and its antimicrobial activity

Authors
Park, Sung YongChung, Jae WooPriestley, Rodney D.Kwak, Seung-Yeop
Issue Date
2012-12
Publisher
SPRINGER
Citation
CELLULOSE, v.19, no.6, pp.2141 - 2151
Abstract
We develop an antimicrobial active robust metal-cellulose nanohybrid by covalent assembly of metal nanoparticles on cellulose fabric using a simple impregnation of thiol-modified cellulose fabric in colloidal silver (Ag) or palladium (Pd) nanoparticle solutions. The combined results of high resolution transmission electron microscopy (HR-TEM), field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDXS) and inductively coupled plasma atomic emission spectrometry (ICP-AES) reveal that the nanoparticles are highly loaded and dispersed in the thiol-modified cellulose fabric, and X-ray photoelectron spectroscopy (XPS) analysis reveals that the nanoparticles are immobilized in the fabric by a strong and stable covalent bond with thiol functional group. This robust covalent linkage between the nanoparticles and the fabric leads to a remarkable suppression of the release of metal nanoparticles from the fabric. In addition, the metal-cellulose nanohybrids show high antimicrobial activity in excess of 99.9 % growth inhibition of the microorganism. Thus, we anticipate that our metal-cellulose nanohybrid may not only protect cell damage caused by penetration and fixation of metal nanoparticles into the human body but also act as a sustainable biomedical textile.
Keywords
IN-SITU SYNTHESIS; SILVER NANOPARTICLES; SOFT ACIDS; ORGANIC-CHEMISTRY; SURFACES; FIBERS; BASES; HARD; PRINCIPLE; CATALYSIS; IN-SITU SYNTHESIS; SILVER NANOPARTICLES; SOFT ACIDS; ORGANIC-CHEMISTRY; SURFACES; FIBERS; BASES; HARD; PRINCIPLE; CATALYSIS; Antimicrobial activity; Covalent bonding; Metal-cellulose nanohybrids; Silver nanoparticles; Palladium nanoparticles
ISSN
0969-0239
URI
https://pubs.kist.re.kr/handle/201004/128612
DOI
10.1007/s10570-012-9773-6
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KIST Article > 2012
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