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Development of a theranostic prodrug for colon cancer therapy by combining ligand-targeted delivery and enzyme-stimulated activation

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dc.contributor.authorSharma, Amit-
dc.contributor.authorKim, Eun-Joong-
dc.contributor.authorShi, Hu-
dc.contributor.authorLee, Jin Yong-
dc.contributor.authorChung, Bong Geun-
dc.contributor.authorKim, Jong Seung-
dc.date.accessioned2021-09-02T15:56:35Z-
dc.date.available2021-09-02T15:56:35Z-
dc.date.created2021-06-16-
dc.date.issued2018-02-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/77881-
dc.description.abstractThe high incidence of colorectal cancer worldwide is currently a major health concern. Although conventional chemotherapy and surgery are effective to some extent, there is always a risk of relapse due to associated side effects, including post-surgical complications and non-discrimination between cancer and normal cells. In this study, we developed a small molecule-based theranostic system, Gal-Dox, which is preferentially taken up by colon cancer cells through receptor-mediated endocytosis. After cancer specific activation, the active drug Dox (doxorubicin) is released with a fluorescence turn-on response, allowing both drug localization and site of action to be monitored. The therapeutic potency of Gal-Dox was also evaluated, both in vivo and ex vivo, thus illustrating the potential of Gal-Dox as a colorectal cancer theranostic with great specificity. (C) 2017 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCI LTD-
dc.subjectASIALOGLYCOPROTEIN RECEPTOR-
dc.subjectSOLID TUMORS-
dc.subjectHEPATOCELLULAR-CARCINOMA-
dc.subjectCOLORECTAL-CANCER-
dc.subjectDRUG-DELIVERY-
dc.subjectIN-VIVO-
dc.subjectSYSTEMS-
dc.subjectENDOCYTOSIS-
dc.subjectCONJUGATE-
dc.subjectPROBE-
dc.titleDevelopment of a theranostic prodrug for colon cancer therapy by combining ligand-targeted delivery and enzyme-stimulated activation-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jong Seung-
dc.identifier.doi10.1016/j.biomaterials.2017.11.019-
dc.identifier.scopusid2-s2.0-85034853580-
dc.identifier.wosid000419539000013-
dc.identifier.bibliographicCitationBIOMATERIALS, v.155, pp.145 - 151-
dc.relation.isPartOfBIOMATERIALS-
dc.citation.titleBIOMATERIALS-
dc.citation.volume155-
dc.citation.startPage145-
dc.citation.endPage151-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Biomaterials-
dc.subject.keywordPlusASIALOGLYCOPROTEIN RECEPTOR-
dc.subject.keywordPlusSOLID TUMORS-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA-
dc.subject.keywordPlusCOLORECTAL-CANCER-
dc.subject.keywordPlusDRUG-DELIVERY-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusSYSTEMS-
dc.subject.keywordPlusENDOCYTOSIS-
dc.subject.keywordPlusCONJUGATE-
dc.subject.keywordPlusPROBE-
dc.subject.keywordAuthorTargeted drug delivery-
dc.subject.keywordAuthorColon cancer-
dc.subject.keywordAuthorTheranostic-
dc.subject.keywordAuthorbeta-Galactosidase-
dc.subject.keywordAuthorDoxorubicin-
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