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DC Field | Value | Language |
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dc.contributor.author | Rungsinee Phongpradist | en_US |
dc.contributor.author | Chuda Chittasupho | en_US |
dc.contributor.author | Siriporn Okonogi | en_US |
dc.contributor.author | Teruna Siahaan | en_US |
dc.contributor.author | Songyot Anuchapreeda | en_US |
dc.contributor.author | Chadarat Ampasavate | en_US |
dc.contributor.author | Cory Berkland | en_US |
dc.date.accessioned | 2018-09-04T04:52:34Z | - |
dc.date.available | 2018-09-04T04:52:34Z | - |
dc.date.issued | 2010-08-20 | en_US |
dc.identifier.issn | 13816128 | en_US |
dc.identifier.other | 2-s2.0-77955646154 | en_US |
dc.identifier.other | 10.2174/138161210791920450 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77955646154&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/51152 | - |
dc.description.abstract | Leukemia therapeutics are aiming for improved efficacy by targeting molecular markers differentially expressed on cancerous cells. Lymphocyte function-associated antigen-1 (LFA-1) expression on various types of leukemia has been well studied. Here, the role and expression of LFA-1 on leukemic cells and the possibility of using this integrin as a target for drug delivery is reviewed. To support this rationale, experimental results were also included where cIBR, a cyclic peptide derived from a binding site of LFA-1, was conjugated to the surface of polymeric nanoparticles and used as a targeting ligand. These studies revealed a correlation of LFA-1 expression level on leukemic cell lines and binding and internalization of cIBR-NPs suggesting a differential binding and internalization of cIBR-NPs to leukemic cells overexpressing LFA-1. Nanoparticles conjugated with a cyclic peptide against an accessible molecular marker of disease hold promise as a selective drug delivery system for leukemia treatment. © 2010 Bentham Science Publishers Ltd. | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | LFA-1 on leukemic cells as a target for therapy or drug delivery | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Current Pharmaceutical Design | en_US |
article.volume | 16 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | University of Kansas Lawrence | en_US |
Appears in Collections: | CMUL: Journal Articles |
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