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dc.contributor.authorTebaldi, Marli Luizapt_BR
dc.contributor.authorLeal, Débora Abrantespt_BR
dc.contributor.authorMontoro, Sérgio Robertopt_BR
dc.contributor.authorPetzhold, Cesar Liberatopt_BR
dc.date.accessioned2014-12-13T02:18:59Zpt_BR
dc.date.issued2014pt_BR
dc.identifier.issn1516-1439pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/108271pt_BR
dc.description.abstractPoly(2-(dimethylamino)ethylmethacrylate-b-methymethacrylate) (PDMAEMA-b-PMMA) poly(2- (dimethylamino)ethylmethacrylate-b-vinylcaprolactam-b-(2-(dimethylamino)ethyl methacrylate) (PDMAEMA-b-PVCL-b-PDMAEMA) and poly(vinylcaprolactam-b-(2-(dimethylamino) ethylmethacrylate-b-vinylcaprolactam) (PVCL-b-PDMAEMA-b-PVCL) block copolymers were obtained by reversible addition-fragmentation chain transfer (RAFT) polymerization, and the effect of the solution pH on the particle size was investigated. In the case of PDMAEMA-b-PMMA, PDMAEMA was first synthesized using 2-cyanoprop-2-yl dithiobenzoate (CPDB) as a chain transfer agent (CTA), which was subsequently used for the RAFT polymerization of MMA. The triblock copolymers were obtained using PDMAEMA or PVCL as macro-CTAs prepared using dibenzyl trithiocarbonate (DBTTC) as a bifunctional RAFT agent. The structure and formation of the copolymers was confirmed through 1H NMR and SEC analysis. The particle size varied considerably depending on the pH of the aqueous solutions of copolymers indicating that these materials could be potential candidates for biomedical applications.en
dc.format.mimetypeapplication/pdf
dc.language.isoengpt_BR
dc.relation.ispartofMaterials research : ibero-american journal of materials. São Carlos. Vol. 17, supl. 1 (2014), p. 191-196pt_BR
dc.rightsOpen Accessen
dc.subjectpoly(dimethylaminoethyl methacrylate)en
dc.subjectCopolímeros em blocopt_BR
dc.subjectReversible additionen
dc.subjectPolimerizaçãopt_BR
dc.subjectfragmentation chain transfer (RAFT) polymerizationen
dc.subjectpoly(methylmethacrylate)en
dc.subjectpoly(vinylcaprolactam)en
dc.titleSynthesis of stimuli-sensitive copolymers by RAFT polymerization : potential candidates as drug delivery systemspt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000947390pt_BR
dc.type.originNacionalpt_BR


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