Publications

Detailed Information

Chitosan-graft-polyethylenimine for Akt1 siRNA delivery to lung cancer cells

DC Field Value Language
dc.contributor.authorJere, Dhananjay-
dc.contributor.authorJiang, Hu-Lin-
dc.contributor.authorKim, You-Kyoung-
dc.contributor.authorArote, Rohidas-
dc.contributor.authorChoi, Yun-Jaie-
dc.contributor.authorYun, Cheol-Heui-
dc.contributor.authorCho, Myung-Haing-
dc.contributor.authorCho, Chong-Su-
dc.date.accessioned2021-01-31T08:43:57Z-
dc.date.available2021-01-31T08:43:57Z-
dc.date.created2018-01-22-
dc.date.issued2009-08-
dc.identifier.citationInternational Journal of Pharmaceutics, Vol.378 No.1-2, pp.194-200-
dc.identifier.issn0378-5173-
dc.identifier.other25280-
dc.identifier.urihttps://hdl.handle.net/10371/172403-
dc.description.abstractEfficient delivery of small interfering RNA (siRNA) remains a challenging task in RNA interference (RNAi) studies. In this study, we used chitosan-graft-polyethylenimine (CHI-g-PEI) copolymer composed of chitosan and low molecular weight polyethylenimine (PEI) for the delivery of siRNA. The CHI-g-PEI carrier formed stable complexes with siRNA with compact spherical morphology. CHI-g-PEI delivered EGFP siRNA (siGFP) silenced EGFP expression nearly 2.5 folds higher than PEI25K at 50 pM siGFP concentration. Cell viability was found to be 2 folds high with CHI-g-PEI carrier than PEI25K. Also, our CHI-g-PEI carrier efficiently delivered Akt1 siRNA (siAkt) and thereby silenced onco-protein Akt1. Silencing of this crucial cell survival protein significantly reduced the lung cancer cell survival and proliferation. Additionally, Akt1 protein knock-down decreased A549 cell malignancy and metastasis. These findings suggest that the CHI-g-PEI carrier efficiently and safely delivered siRNA. Moreover, CHI-g-PEI mediated Akt1 siRNA delivery may immerge as a viable approach for lung cancer treatment. (C) 2009 Elsevier B.V. All rights reserved.-
dc.language영어-
dc.publisherElsevier BV-
dc.titleChitosan-graft-polyethylenimine for Akt1 siRNA delivery to lung cancer cells-
dc.typeArticle-
dc.contributor.AlternativeAuthor조명행-
dc.identifier.doi10.1016/j.ijpharm.2009.05.046-
dc.citation.journaltitleInternational Journal of Pharmaceutics-
dc.identifier.wosid000269163600029-
dc.identifier.scopusid2-s2.0-67650608146-
dc.citation.endpage200-
dc.citation.number1-2-
dc.citation.startpage194-
dc.citation.volume378-
dc.identifier.sci000269163600029-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorArote, Rohidas-
dc.contributor.affiliatedAuthorChoi, Yun-Jaie-
dc.contributor.affiliatedAuthorYun, Cheol-Heui-
dc.contributor.affiliatedAuthorCho, Myung-Haing-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusCELLULAR-SURVIVAL-
dc.subject.keywordPlusGENE CARRIER-
dc.subject.keywordPlusADENOCARCINOMA-
dc.subject.keywordPlusVIVO-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordAuthorPolymeric carrier-
dc.subject.keywordAuthorNon-viral vector-
dc.subject.keywordAuthorSiRNA delivery-
dc.subject.keywordAuthorAkt-
dc.subject.keywordAuthorChitosan-
dc.subject.keywordAuthorPolyethylenimine-
dc.subject.keywordAuthorLung cancer-
Appears in Collections:
Files in This Item:
There are no files associated with this item.

Related Researcher

  • College of Veterinary Medicine
  • Department of Veterinary Medicine
Research Area Nanotoxicology, Veterinary Toxicology

Altmetrics

Item View & Download Count

  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Share