Source:http://linkedlifedata.com/resource/pubmed/id/15032738
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
Pt 2
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pubmed:dateCreated |
2004-3-22
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pubmed:abstractText |
Silica nanoparticles were prepared in a microemulsion system, using polyoxyethylene nonylphenyl ether/cyclohexane/ammonium hydroxide. The surface charge of the particle was modified with PLL [poly(L-lysine)]. PAGE demonstrated the ability of PMS-NP (PLL-modified silica nanoparticles) to bind and protect antisense ODNs (oligonucleotides). The intracellular localization of FITC-labelled ODN was investigated by fluorescence microscopy. The results demonstrated that ODN could be delivered to cytoplasm. Flow-cytometry analysis showed a 20-fold enhancement of ODN delivered by PMS-NP compared with free ODN for a serum-free medium. Blocking efficacy of c- myc antisense ODN, delivered by PMS-NP, was examined in HNE1 and HeLa cell lines. Significant down-regulation of c- myc mRNA levels was observed in both the cell lines. However, the cellular uptake efficiency and antisense effects on target gene decreased in the presence of serum-containing medium. The analysis of the filtration assay showed that PMS-NP interacted with serum proteins. These results indicated that PMS-NP was a suitable delivery vector for antisense ODN, although its delivery efficiency decreased in the presence of a serum-containing medium.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Coated Materials, Biocompatible,
http://linkedlifedata.com/resource/pubmed/chemical/Drug Carriers,
http://linkedlifedata.com/resource/pubmed/chemical/Oligoribonucleotides, Antisense,
http://linkedlifedata.com/resource/pubmed/chemical/Polylysine,
http://linkedlifedata.com/resource/pubmed/chemical/Silicon Dioxide
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0885-4513
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pubmed:author |
pubmed-author:LiGui-YuanGY,
pubmed-author:LiXiao-LingXL,
pubmed-author:LuHong-BinHB,
pubmed-author:NieXin-MinXM,
pubmed-author:ShenShou-RongSR,
pubmed-author:TangKeK,
pubmed-author:XiangJuan-JuanJJ,
pubmed-author:XiongWeiW,
pubmed-author:ZhangBi-ChengBC,
pubmed-author:ZhouJieJ,
pubmed-author:ZhouMingM,
pubmed-author:ZhuShi-GuoSG
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pubmed:issnType |
Print
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pubmed:volume |
39
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
179-87
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pubmed:dateRevised |
2007-3-21
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pubmed:meshHeading |
pubmed-meshheading:15032738-Carcinoma,
pubmed-meshheading:15032738-Cell Line, Tumor,
pubmed-meshheading:15032738-Coated Materials, Biocompatible,
pubmed-meshheading:15032738-Drug Carriers,
pubmed-meshheading:15032738-Gene Transfer Techniques,
pubmed-meshheading:15032738-HeLa Cells,
pubmed-meshheading:15032738-Humans,
pubmed-meshheading:15032738-Materials Testing,
pubmed-meshheading:15032738-Nanotubes,
pubmed-meshheading:15032738-Oligoribonucleotides, Antisense,
pubmed-meshheading:15032738-Particle Size,
pubmed-meshheading:15032738-Polylysine,
pubmed-meshheading:15032738-Silicon Dioxide,
pubmed-meshheading:15032738-Surface Properties,
pubmed-meshheading:15032738-Tissue Distribution,
pubmed-meshheading:15032738-Transfection
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pubmed:year |
2004
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pubmed:articleTitle |
Poly(L-lysine)-modified silica nanoparticles for the delivery of antisense oligonucleotides.
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pubmed:affiliation |
Cancer Research Institute, XiangYa School of Medicine, Central South University, ChangSha, HuNan 410078, People's Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Evaluation Studies
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