Folate receptor mediated intracellular protein delivery using PLL-PEG-FOL conjugate

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dc.contributor.authorKim, SHko
dc.contributor.authorJeong, JHko
dc.contributor.authorJoe, Cheol Oko
dc.contributor.authorPark, TGko
dc.date.accessioned2009-11-23T05:19:09Z-
dc.date.available2009-11-23T05:19:09Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2005-04-
dc.identifier.citationJOURNAL OF CONTROLLED RELEASE, v.103, no.3, pp.625 - 634-
dc.identifier.issn0168-3659-
dc.identifier.urihttp://hdl.handle.net/10203/13111-
dc.description.abstractTo develop a receptor-mediated intracellular delivery system that can transport therapeutic proteins or other bioactive macromolecules into a specific cell, a di-block copolymer conjugate, poly(L-lysine)-polyethylene glycol)-folate (PLL-PEG-FOL), was synthesized. The PLL-PEG-FOL conjugate was physically complexed with fluorescein isothiocyanate conjugated bovine serum albumin (FITC-BSA) in an aqueous phase by ionic interactions. Cellular uptake of PLL-PEG-FOL/FITC-BSA complexes was greatly enhanced against a folate receptor over-expressing cell line (KB cells) compared to a folate receptor deficient cell line (A549 cells). The presence of an excess amount of free folate (1 mM) in the medium inhibited the intracellular delivery of PLL-PEG-FOL/FITC-BSA complexes. This suggests that the enhanced cellular uptake of FITC-BSA by KB cells in a specific manner was attributed to folate receptor-mediated endocytosis of the complexes having folate moieties on the surface. The PLL-PEG-FOL di-block copolymer could be potentially applied for intracellular delivery of a wide range of other biological active agents that have negative charges on the surface. (c) 2005 Elsevier B.V All rights reserved.-
dc.description.sponsorshipNational Cancer Center (02-3-150) and the Ministry of Science and Technology (M10214000117- 02b1500-02110), Republic of Korea.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherElsevier Science Bv-
dc.subjectPOLYION COMPLEX MICELLES-
dc.subjectENTRAPPING ENZYME MOLECULES-
dc.subjectDRUG-DELIVERY-
dc.subjectBLOCK-COPOLYMER-
dc.subjectANTISENSE OLIGONUCLEOTIDE-
dc.subjectGENE DELIVERY-
dc.subjectTARGETED DRUG-
dc.subjectCELLS-
dc.subjectPEPTIDE-
dc.subjectSYSTEM-
dc.titleFolate receptor mediated intracellular protein delivery using PLL-PEG-FOL conjugate-
dc.typeArticle-
dc.identifier.wosid000228715500008-
dc.identifier.scopusid2-s2.0-16344382196-
dc.type.rimsART-
dc.citation.volume103-
dc.citation.issue3-
dc.citation.beginningpage625-
dc.citation.endingpage634-
dc.citation.publicationnameJOURNAL OF CONTROLLED RELEASE-
dc.identifier.doi10.1016/j.jconrel.2004.01.006-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorJoe, Cheol O-
dc.contributor.localauthorPark, TG-
dc.contributor.nonIdAuthorKim, SH-
dc.contributor.nonIdAuthorJeong, JH-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorfolate-
dc.subject.keywordAuthorintracellular protein delivery-
dc.subject.keywordAuthortargeting-
dc.subject.keywordAuthorPLL-PEG-FOL conjugate-
dc.subject.keywordPlusPOLYION COMPLEX MICELLES-
dc.subject.keywordPlusENTRAPPING ENZYME MOLECULES-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusBLOCK-COPOLYMER-
dc.subject.keywordPlusANTISENSE OLIGONUCLEOTIDE-
dc.subject.keywordPlusGENE DELIVERY-
dc.subject.keywordPlusTARGETED DRUG-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusPEPTIDE-
dc.subject.keywordPlusSYSTEM-
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