dc.contributor.author | Ahmadkhani, L | |
dc.contributor.author | Akbarzadeh, A | |
dc.contributor.author | Abbasian, M | |
dc.date.accessioned | 2018-08-26T07:12:41Z | |
dc.date.available | 2018-08-26T07:12:41Z | |
dc.date.issued | 2018 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44778 | |
dc.description.abstract | A 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.iso | English | |
dc.relation.ispartof | ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY | |
dc.subject | Smart drug delivery system | |
dc.subject | RAFT polymerization | |
dc.subject | stimuli-sensitive triblock terpolymer | |
dc.subject | magnetic iron oxide nanoparticles | |
dc.subject | drug-loading efficiency | |
dc.title | Development and characterization dual responsive magnetic nanocomposites for targeted drug delivery systems | |
dc.type | Article | |
dc.citation.volume | 46 | |
dc.citation.issue | 5 | |
dc.citation.spage | 1052 | |
dc.citation.epage | 1063 | |
dc.citation.index | Web of science | |
dc.identifier.DOI | https://doi.org/10.1080/21691401.2017.1360323 | |