Controlled silver nanoparticles synthesis in semi-hydrogel networks of poly(acrylamide) and carbohydrates: A rational methodology for antibacterial application

被引:255
作者
Vimala, K. [1 ]
Sivudu, K. Samba [1 ]
Mohan, Y. Murali [1 ]
Sreedhar, B. [2 ]
Raju, K. Mohana [1 ]
机构
[1] Sri Krishnadevaraya Univ, Dept Polymer Sci & Technol, Synthet Polymer Lab, Anantapur 515003, Andhra Pradesh, India
[2] Indian Inst Chem Technol, Hyderabad 500007, Andhra Pradesh, India
关键词
Silver nanoparticles; Carboxymethyl cellulose; Gum Acacia; Starch; Autoreduction; Antibacterial activity; Biomedical application; GREEN SYNTHESIS; CARBOXYMETHYL CELLULOSE; STABILIZED SILVER; HYBRID MICROGELS; METAL; POLYMER; GOLD; REDUCTION; PLATINUM; NANOCOMPOSITES;
D O I
10.1016/j.carbpol.2008.08.009
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In the present study, we report the preparation of semi interpenetrating hydrogel networks (SIHNs) based on cross-linked poly (acrylamide) prepared through an optimized rapid redox-solution polymerization with N,N'-methylenebisacrylamide (MBA) in presence of three different carbohydrate polymers, namely gum acacia (GA), carboxymethylcellulose (CMC) and starch (SR). Highly stable and uniformly distributed silver nanoparticles have been obtained with hydrogel networks as nanoreactors via in situ reduction of silver nitrate (AgNO3) using sodium borohydride (NaBH4) as reducing agent. The formation of silver nanoparticles has been confirmed with ultraviolet visible (UV-vis) spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD) analyses. Thermogravimetric analysis (TGA) provides the amounts of silver nanoparticles exist in the hydrogel networks. Transmission electron microscopy (TEM) results demonstrate that acacia employed hydrogels have regulated the silver nanoparticles size to 2-5 run where as CIVIC and starch composed hydrogel networks result in a heterogeneous size front 2 to 20 nm. The preliminary antibacterial activity performed to these hydrogel-silver nanocomposites. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:463 / 471
页数:9
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