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dc.contributor.authorMotaali, S
dc.contributor.authorPashaeiasl, M
dc.contributor.authorAkbarzadeh, A
dc.contributor.authorDavaran, S
dc.date.accessioned2018-08-26T05:37:54Z
dc.date.available2018-08-26T05:37:54Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/39960
dc.description.abstractIn the present study, magnetic and thermo/pH-sensitive (multiresponsive) nanocomposites based on N-isopropylacrylamide (NIPAAM) were synthesized and characterized. Nanocomposites were synthesized by free radical emulsion polymerization of NIPAAM as thermosensitive monomer and N,N-dimethyl-aminoethyl methacrylate (DMAEMA) as pH-sensitive monomer in the presence of methylene-bis-acrylamide as cross-linking agent. Doxorubicin, an anti-cancer drug, was loaded into these nanocomposites via equilibrium swelling method. Thermo/pH-sensitive cross-linked poly (NIPAAM-DMAEMA)-Fe3O4 nanocomposites were characterized by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and vibrating sample magnetometer (VSM). The volume of the loaded drug and drug release amount was determined by UV measurements. The results showed that this thermo/pH-sensitive magnetic nanocomposite has a high drug-loading efficiency. Doxorubicin was released at 40?آ°C and pH 5.8 more than the 37?آ°C and pH 7.4.
dc.language.isoEnglish
dc.relation.ispartofArtificial cells, nanomedicine, and biotechnology
dc.subjectAcrylamides
dc.subjectAntineoplastic Agents
dc.subjectCross-Linking Reagents
dc.subjectDoxorubicin
dc.subjectDrug Carriers
dc.subjectDrug Compounding
dc.subjectDrug Liberation
dc.subjectFerrosoferric Oxide
dc.subjectHydrogen-Ion Concentration
dc.subjectKinetics
dc.subjectMagnets
dc.subjectMethacrylates
dc.subjectNanocomposites
dc.subjectParticle Size
dc.subjectPolymerization
dc.subjectTemperature
dc.titleSynthesis and characterization of smart N-isopropylacrylamide-based magnetic nanocomposites containing doxorubicin anti-cancer drug.
dc.typearticle
dc.citation.volume45
dc.citation.issue3
dc.citation.spage560
dc.citation.epage567
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.3109/21691401.2016.1161640


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