膜
纳米团簇
壳聚糖
药物输送
生物相容性
微型多孔材料
聚乙二醇
PEG比率
化学
材料科学
化学工程
核化学
纳米技术
有机化学
生物化学
经济
工程类
财务
作者
Saket Mishra,Subina Raveendran,J.M.F. Ferreira,S. Kannan
出处
期刊:Langmuir
[American Chemical Society]
日期:2016-09-29
卷期号:32 (40): 10305-10316
被引量:43
标识
DOI:10.1021/acs.langmuir.6b02844
摘要
An in situ synthesis method for preparing silver nanoclusters (AgNCs) embedded in chitosan-polyethylene glycol (CS-PEG) membranes is disclosed. The aim is to develop implantable multifunctional devices for biofilm inhibition and drug release to reduce percutaneous device related complications (PDRCs). A multiple array of characterization techniques confirmed the formation of fluorescent AgNCs with sizes of ∼3 nm uniformly distributed in CS-PEG matrix and their active role in determining the fraction and interconnectivity of the microporous membranes. The presence and increasing contents of AgNCs enhanced the mechanical stability of membranes and decreased their susceptibility to degradation in the presence of lysozyme and H2O2. Moreover, the presence and increasing concentrations of AgNCs hindered biofilm formation against Escherichia coli (Gram negative) and Staphylococcus aureus (Gram positive) and enabled a sustainable release of an anti-inflammatory drug naproxen in vitro until 24 h. The overall results gathered and reported in this work make the AgNCs impregnated CS-PEG membranes highly promising multifunctional devices combining efficient antibacterial activity and biocompatibility with active local drug delivery.
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