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dc.contributor.authorAhmadkhani, L
dc.contributor.authorAkbarzadeh, A
dc.contributor.authorAbbasian, M
dc.date.accessioned2018-08-26T07:12:41Z
dc.date.available2018-08-26T07:12:41Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44778
dc.description.abstractA drug delivery system based on dual responsive units was developed. An appealing pH-and thermo-responsive triblock terpolymer as the drug carrier was synthesized by RAFT polymerization of N-isopropyl acrylamide and methacrylic acid monomers using PEG-RAFT agent. The Fe3O4 magnetic nanoparticles were synthesized by co-precipitation of Fe salts. Synthesized samples were characterized by FT-IR, XRD, GPC, SEM and TEM. The dual responsive behaviour and self-assembly of the triblock terpolymers in aqueous solution were investigated using UV-vis transmittance and DLS. Based on the results of DLS and TEM, the average size of micelles was 170, 125 and 30 nm. The triblock terpolymer was used as a chemotherapy drug carrier and doxorubicin as a model drug. The release rate of the drug at two different temperatures (37 degrees C and 42 degrees C) and pHs (5.8 and 7.4) was studied. The in vitro cytotoxicity assay of free doxorubicin and drug-loaded magnetic nanoparticles was studied. The MTT assay exhibited that these polymers are biocompatible and no toxicity. As well, IC50 of the DOX-loaded triblock terpolymer in MTT test demonstrated that these systems could be suitable for the treatment of cancer.
dc.language.isoEnglish
dc.relation.ispartofARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY
dc.subjectSmart drug delivery system
dc.subjectRAFT polymerization
dc.subjectstimuli-sensitive triblock terpolymer
dc.subjectmagnetic iron oxide nanoparticles
dc.subjectdrug-loading efficiency
dc.titleDevelopment and characterization dual responsive magnetic nanocomposites for targeted drug delivery systems
dc.typeArticle
dc.citation.volume46
dc.citation.issue5
dc.citation.spage1052
dc.citation.epage1063
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1080/21691401.2017.1360323


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