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dc.contributor.authorPark, Jae Hyung-
dc.contributor.authorSaravanakumar, Gurusamy-
dc.contributor.authorKim, Kwangmeyung-
dc.contributor.authorKwon, Ick Chan-
dc.date.accessioned2024-01-20T20:01:51Z-
dc.date.available2024-01-20T20:01:51Z-
dc.date.created2021-09-02-
dc.date.issued2010-01-31-
dc.identifier.issn0169-409X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/131769-
dc.description.abstractChitosan has prompted the continuous impetus for the development of safe and effective drug delivery systems because of its unique physicochemical and biological characteristics. The primary hydroxyl and amine groups located on the backbone of chitosan allow for chemical modification to control its physical properties. When the hydrophobic moiety is conjugated to a chitosan molecule, the resulting amphiphile may form self-assembled nanoparticles that can encapsulate a quantity of drugs and deliver them to a specific site of action. Chemical attachment of the drug to the chitosan throughout the functional linker may produce useful prodrugs, exhibiting the appropriate biological activity at the target site. Mucoadhesive and absorption enhancement properties of chitosan increase the in vivo residence time of the dosage form in the gastrointestinal tract and improve the bioavailability of various drugs. The main objective of this review is to provide an insight into various target-specific carriers, based on chitosan and its derivatives, towards low molecular weight drug delivery. The first part of the review is concerned with the organ-specific delivery of low molecular drugs using chitosan and its derivatives. The subsequent section considers the recent developments of drug delivery carriers for cancer therapy with special focus on various targeting strategies. (C) 2009 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectSELF-ASSEMBLED NANOPARTICLES-
dc.subjectMODIFIED GLYCOL CHITOSAN-
dc.subjectN-SUCCINYL-CHITOSAN-
dc.subjectCOLON-SPECIFIC DELIVERY-
dc.subjectO-SULFATE CHITOSAN-
dc.subjectPOLYION COMPLEX MICELLES-
dc.subjectTRANS-RETINOIC ACID-
dc.subjectIN-VITRO EVALUATION-
dc.subjectPOLYELECTROLYTE COMPLEXES-
dc.subjectPOLYMERIC MICELLES-
dc.titleTargeted delivery of low molecular drugs using chitosan and its derivatives-
dc.typeArticle-
dc.identifier.doi10.1016/j.addr.2009.10.003-
dc.description.journalClass1-
dc.identifier.bibliographicCitationADVANCED DRUG DELIVERY REVIEWS, v.62, no.1, pp.28 - 41-
dc.citation.titleADVANCED DRUG DELIVERY REVIEWS-
dc.citation.volume62-
dc.citation.number1-
dc.citation.startPage28-
dc.citation.endPage41-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000275134500004-
dc.identifier.scopusid2-s2.0-75149147998-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeReview-
dc.subject.keywordPlusSELF-ASSEMBLED NANOPARTICLES-
dc.subject.keywordPlusMODIFIED GLYCOL CHITOSAN-
dc.subject.keywordPlusN-SUCCINYL-CHITOSAN-
dc.subject.keywordPlusCOLON-SPECIFIC DELIVERY-
dc.subject.keywordPlusO-SULFATE CHITOSAN-
dc.subject.keywordPlusPOLYION COMPLEX MICELLES-
dc.subject.keywordPlusTRANS-RETINOIC ACID-
dc.subject.keywordPlusIN-VITRO EVALUATION-
dc.subject.keywordPlusPOLYELECTROLYTE COMPLEXES-
dc.subject.keywordPlusPOLYMERIC MICELLES-
dc.subject.keywordAuthorChitosan-
dc.subject.keywordAuthorLow molecular drugs-
dc.subject.keywordAuthorTargeted delivery-
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