Source:http://linkedlifedata.com/resource/pubmed/id/18508209
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2008-6-3
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pubmed:abstractText |
A systematic study on the in vitro interactions of 7-20 nm spherical silver nanoparticles (SNP) with HT-1080 and A431 cells was undertaken as a part of an on-going program in our laboratory to develop a topical antimicrobial agent for the treatment of burn wound infections. Upon exposure to SNP (up to 6.25 microg/mL), morphology of both the cell types remained unaltered. However, at higher concentrations (6.25-50 microg/mL) cells became less polyhedral, more fusiform, shrunken and rounded. IC(50) values for HT-1080 and A431 as revealed by XTT assay were 10.6 and 11.6 microg/mL, respectively. When the cells were challenged with approximately 1/2 IC(50) concentration of SNP (6.25 microg/mL), clear signs of oxidative stress, i.e. decreased GSH ( approximately 2.5-folds in HT-1080, approximately 2-folds in A431) and SOD ( approximately 1.6-folds in HT-1080, 3-folds in A431) as well as increased lipid peroxidation ( approximately 2.5-folds in HT-1080, approximately 2-folds in A431) were seen. Changes in the levels of catalase and GPx in A431 cells were statistically insignificant in both cell types. DNA fragmentation in SNP-exposed cells suggested apoptosis. When the apoptotic thresholds of SNP were monitored with caspase-3 assay the concentrations required for the onset of apoptosis were found to be much lower (0.78 microg/mL in HT-1080, 1.56 microg/mL in A431) than the necrotic concentration (12.5 microg/mL in both cell types). These results can be used to define a safe range of SNP for the intended application as a topical antimicrobial agent after appropriate in vivo studies.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0378-4274
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
30
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pubmed:volume |
179
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
93-100
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pubmed:meshHeading |
pubmed-meshheading:18508209-Apoptosis,
pubmed-meshheading:18508209-Catalase,
pubmed-meshheading:18508209-Cell Line, Tumor,
pubmed-meshheading:18508209-Cell Survival,
pubmed-meshheading:18508209-DNA Fragmentation,
pubmed-meshheading:18508209-Glutathione Peroxidase,
pubmed-meshheading:18508209-Humans,
pubmed-meshheading:18508209-Lipid Peroxidation,
pubmed-meshheading:18508209-Metal Nanoparticles,
pubmed-meshheading:18508209-Particle Size,
pubmed-meshheading:18508209-Silver,
pubmed-meshheading:18508209-Superoxide Dismutase
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pubmed:year |
2008
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pubmed:articleTitle |
Cellular responses induced by silver nanoparticles: In vitro studies.
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pubmed:affiliation |
Centre for Nanobioscience, Agharkar Research Institute, G.G. Agarkar Road, Pune 411004, India.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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