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dc.contributor.authorToomari, Y
dc.contributor.authorNamazi, H
dc.contributor.authorAkbar, EA
dc.date.accessioned2018-08-26T05:42:37Z
dc.date.available2018-08-26T05:42:37Z
dc.date.issued2015
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/40646
dc.description.abstractThe objective of this study was the syntheses of well-defined glycodendrimer with entrapment efficiency by click reactions, with ?-cyclodextrins (?-CDs) moiety to keep the biocompatibility properties, besides especially increase their capacity to load numerous appropriate sized guests. The original dendrimer containing ?-CD in both periphery and central was synthesized using click reaction. The entrapment property of the ?-CD-dendrimer was studied by methotrexate (MTX) drug. The chemical structure of ?-CD-dendrimer was characterized by (1)H NMR, (13)C NMR and FTIR and its inclusion complex structure were investigated by SEM, DLS, DSC and FTIR techniques. The cytotoxic effect of obtained compound and its inclusion complex with MTX was analyzed using MTT test. The MTT test exhibited that the synthesized compound was not cytotoxic to the cell line considered. The in vitro drug release study turned out that the obtained ?-CD dendrimer could be a suitable controlled drug delivery system for cancer treatment.
dc.language.isoEnglish
dc.relation.ispartofCarbohydrate polymers
dc.subjectAntimetabolites, Antineoplastic
dc.subjectCell Line, Tumor
dc.subjectClick Chemistry
dc.subjectDelayed-Action Preparations
dc.subjectDendrimers
dc.subjectHumans
dc.subjectMethotrexate
dc.subjectNeoplasms
dc.subjectbeta-Cyclodextrins
dc.titleSynthesis of the dendritic type ?-cyclodextrin on primary face via click reaction applicable as drug nanocarrier.
dc.typearticle
dc.citation.volume132
dc.citation.spage205
dc.citation.epage13
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1016/j.carbpol.2015.05.087


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