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dc.contributor.author윤채옥-
dc.date.accessioned2017-06-13T02:47:20Z-
dc.date.available2017-06-13T02:47:20Z-
dc.date.issued2015-09-
dc.identifier.citationCOLLOIDS AND SURFACES B-BIOINTERFACES, v. 133, Page. 254-262en_US
dc.identifier.issn0927-7765-
dc.identifier.issn1873-4367-
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S0927776515003914-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/27767-
dc.description.abstractIn this study, we report the development of a novel, redox-sensitive chitosan-based targeted drug delivery system, containing two drugs. We determined whether the synthesized polymeric micelles (HPTOC-DOX) were suitable as a drug carrier. The formation of HPTOC-DOX micelles was confirmed by H-1 NMR. HPTOC-DOX formed micelles of approximately 151.9 similar to 311.2 nm in size in aqueous solution. Analysis of the drug release profile of HPTOC-DOX in different pH conditions (pH 5.2, 6.2, and 7.4) indicated that DOX was released from HPTOC-DOX micelles at acidic pH (5.2 or 6.2), while almost no DOX was released at pH 7.4. In vitro cell cytotoxicity and hemolysis assays indicated that HPTOC-DOX micelles safely deliver anti-cancer drugs and decrease the cytotoxicity of DOX. In vitro anti-cancer activity assays, confocal laser scanning microscopy analysis of SK-BR-3 cells, and in vivo anti-tumor activity in SK-BR-3-derived tumor-bearing mice were used to evaluate synergistic drug effects and the effect of the targeting peptide (anti-human epidermal growth factor receptor 2 [HER2] target peptide, epitope form; LTVSPWY) on receptor-mediated endocytosis. (C) 2015 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipThis work was supported by the National Research Foundation of Korea (NRF) grant funded by the Ministry of Science, ICT & Future Planning (NRF-2014R1A2A1A10053027).en_US
dc.language.isoenen_US
dc.publisherELSEVIER SCIENCE BVen_US
dc.subjectChitosanen_US
dc.subjectDoxorubicinen_US
dc.subjectpH-sensitiveen_US
dc.subjectTargeted deliveryen_US
dc.titleTargeting delivery of tocopherol and doxorubicin grafted-chitosan polymeric micelles for cancer therapy: In vitro and in vivo evaluationen_US
dc.typeArticleen_US
dc.relation.volume133-
dc.identifier.doi10.1016/j.colsurfb.2015.06.018-
dc.relation.page254-262-
dc.relation.journalCOLLOIDS AND SURFACES B-BIOINTERFACES-
dc.contributor.googleauthorNam, Joung-Pyo-
dc.contributor.googleauthorLee, Kyeong-Jae-
dc.contributor.googleauthorChoi, Joung-Woo-
dc.contributor.googleauthorYun, Chae-Ok-
dc.contributor.googleauthorNah, Jae-Woon-
dc.relation.code2015001660-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDEPARTMENT OF BIOENGINEERING-
dc.identifier.pidchaeok-
dc.identifier.researcherIDP-3698-2015-
dc.identifier.orcidhttp://orcid.org/0000-0002-9466-4531-
Appears in Collections:
COLLEGE OF ENGINEERING[S](공과대학) > BIOENGINEERING(생명공학과) > Articles
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