Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/51152
Full metadata record
DC FieldValueLanguage
dc.contributor.authorRungsinee Phongpradisten_US
dc.contributor.authorChuda Chittasuphoen_US
dc.contributor.authorSiriporn Okonogien_US
dc.contributor.authorTeruna Siahaanen_US
dc.contributor.authorSongyot Anuchapreedaen_US
dc.contributor.authorChadarat Ampasavateen_US
dc.contributor.authorCory Berklanden_US
dc.date.accessioned2018-09-04T04:52:34Z-
dc.date.available2018-09-04T04:52:34Z-
dc.date.issued2010-08-20en_US
dc.identifier.issn13816128en_US
dc.identifier.other2-s2.0-77955646154en_US
dc.identifier.other10.2174/138161210791920450en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77955646154&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/51152-
dc.description.abstractLeukemia 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.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleLFA-1 on leukemic cells as a target for therapy or drug deliveryen_US
dc.typeJournalen_US
article.title.sourcetitleCurrent Pharmaceutical Designen_US
article.volume16en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of Kansas Lawrenceen_US
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.