Chitosan coating of copper nanoparticles reduces in vitro toxicity and increases inflammation in the lung.

Chitosan coating of copper nanoparticles reduces in vitro toxicity and increases inflammation in the lung.
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DOI:
10.1088/0957-4484/24/39/395101
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发表时间:
2013-10-04
期刊:
影响因子:
3.5
通讯作者:
Salem AK
Salem AK
中科院分区:
材料科学3区
文献类型:
--
作者:
Worthington KL;Adamcakova-Dodd A;Wongrakpanich A;Mudunkotuwa IA;Mapuskar KA;Joshi VB;Allan Guymon C;Spitz DR;Grassian VH;Thorne PS;Salem AK

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Despite their potential for a variety of applications, copper nanoparticles induce very strong inflammatory responses and cellular toxicity following aerosolized delivery. Coating metallic nanoparticles with polysaccharides, such as biocompatible and antimicrobial chitosan, has the potential to reduce this toxicity. In this study, copper nanoparticles were coated with chitosan using a newly developed and facile method. The presence of coating was confirmed using x-ray photoelectron spectroscopy (XPS), rhodamine tagging of chitosan followed by confocal fluorescence imaging of coated particles, observed increases in particle size and zeta potential. Further physical and chemical characteristics were evaluated using dissolution and x-ray diffraction (XRD) studies. The chitosan coating was shown to significantly reduce the toxicity of copper nanoparticles after 24 and 52 hours and the generation of reactive oxygen species as assayed by DHE oxidation after 24 hours in vitro. Conversely, inflammatory response, measured using the number of white blood cells, total protein, and cytokines/chemokines in the broncheoalveolar fluid of mice exposed to chitosan coated versus uncoated copper nanoparticles, was shown to increase, as was the concentration of copper ions. These results suggest that coating metal nanoparticles with mucoadhesive polysaccharides (e.g. chitosan) could increase their potential for use in controlled release of copper ions to cells, but will result in a higher inflammatory response if administered via the lung.
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