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Cited 11 time in webofscience Cited 15 time in scopus
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dc.contributor.authorPatil, SP-
dc.contributor.authorKim, SH-
dc.contributor.authorJadhav, JR-
dc.contributor.authorLee, JH-
dc.contributor.authorJeon, EM-
dc.contributor.authorKim, KT-
dc.contributor.authorKim, BH-
dc.date.accessioned2016-04-01T07:38:19Z-
dc.date.available2016-04-01T07:38:19Z-
dc.date.created2015-02-04-
dc.date.issued2014-08-
dc.identifier.issn1043-1802-
dc.identifier.other2014-OAK-0000031193-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/26718-
dc.description.abstractThis paper describes the synthesis, characterization, and in vitro and in vivo siRNA transfection ability of B vitamin-based cationic clickable bolaamphiphiles (VBs). Our VBs derived from vitamins B-2, B-3, B-5, B-6, and B-7 formed nanoassembled low-molecular-weight hydrogelators (LMWGs, vitagels). The vitagels VB2, VB6, and VB7 (derived from vitamins B-2, B-6, and B-7, respectively) facilitated delivery of small interfering RNAs (siRNA), efficiently silencing gene expression specifically into cancer cell lines; in addition, the LMWGs derived from vitamins B-3, B-5, and B-6 were biocompatible. An ex vivo study in a mouse model revealed that the siRNA delivered by the vitagel VB7 was located primarily at the site of the tumor. The gene silencing efficiency of vascular endothelial growth factor siRNA delivered by vitagels was dependent on the nature of the vitamin headgroup, the N/P ratio, and, interestingly, the hydrogelation properties of the VBs.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.relation.isPartOfBIOCONJUGATE CHEMISTRY-
dc.titleCancer-Specific Gene Silencing through Therapeutic siRNA Delivery with B Vitamin-Based Nanoassembled Low-Molecular-Weight Hydrogelators-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1021/BC500249G-
dc.author.googlePatil, SP-
dc.author.googleKim, SH-
dc.author.googleJadhav, JR-
dc.author.googleLee, JH-
dc.author.googleJeon, EM-
dc.author.googleKim, KT-
dc.author.googleKim, BH-
dc.relation.volume25-
dc.relation.issue8-
dc.relation.startpage1517-
dc.relation.lastpage1525-
dc.contributor.id10142056-
dc.relation.journalBIOCONJUGATE CHEMISTRY-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOCONJUGATE CHEMISTRY, v.25, no.8, pp.1517 - 1525-
dc.identifier.wosid000340735900019-
dc.date.tcdate2019-02-01-
dc.citation.endPage1525-
dc.citation.number8-
dc.citation.startPage1517-
dc.citation.titleBIOCONJUGATE CHEMISTRY-
dc.citation.volume25-
dc.contributor.affiliatedAuthorKim, KT-
dc.contributor.affiliatedAuthorKim, BH-
dc.identifier.scopusid2-s2.0-84906334255-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc7-
dc.description.scptc8*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusAMINO-ACID-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusRNA-
dc.subject.keywordPlusEFFICIENCY-
dc.subject.keywordPlusPOLYMERS-
dc.subject.keywordPlusGELATION-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-

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김경태KIM, KYONG TAI
Dept of Life Sciences
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