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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
1984-10-12
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pubmed:abstractText |
Polyalkyl cyanoacrylate nanoparticles were previously developed as a biodegradable, ultrafine, solid drug carrier. Distribution studies in the rat showed an intense and rapid hepatic uptake. This liver accumulation appears to represent, to a certain extent, extracellularly bound nanoparticles. During liver perfusion, 15-20% of the liver-associated nanoparticles were washed out. The cellular distribution of strongly cell-associated nanoparticles was determined. At different intervals after injection of radioactive nanoparticles to rats, the cells were isolated according to a recently developed, low-temperature procedure during which processing of the carrier was inhibited. At all tested times, a relatively intense capture by Kupffer cells in comparison with endothelial and especially parenchymal cells was observed. This distribution pattern was not influenced by the size of the nanoparticles (0.08-0.215-micron diameter). This specific interaction of nanoparticles with Kupffer cells opens possibilities for the treatment of some parasitic diseases involving this cell type.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
|
pubmed:issn |
0022-3549
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
73
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
980-2
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6470966-Animals,
pubmed-meshheading:6470966-Bucrylate,
pubmed-meshheading:6470966-Cyanoacrylates,
pubmed-meshheading:6470966-Endothelium,
pubmed-meshheading:6470966-Kinetics,
pubmed-meshheading:6470966-Kupffer Cells,
pubmed-meshheading:6470966-Liver,
pubmed-meshheading:6470966-Microspheres,
pubmed-meshheading:6470966-Rats,
pubmed-meshheading:6470966-Rats, Inbred Strains
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pubmed:year |
1984
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pubmed:articleTitle |
In vivo uptake of polyisobutyl cyanoacrylate nanoparticles by rat liver Kupffer, endothelial, and parenchymal cells.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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