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dc.contributor.authorNosrati, H
dc.contributor.authorSalehiabar, M
dc.contributor.authorKheiri Manjili, H
dc.contributor.authorDavaran, S
dc.contributor.authorDanafar, H
dc.date.accessioned2018-08-26T09:42:16Z
dc.date.available2018-08-26T09:42:16Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/58533
dc.description.abstractIn this work, we reported the synthesis of curcumin (CUR)-loaded hydrophilic and hydrophobic natural amino acids (AAs)-modified iron oxide magnetic nanoparticles (IONPs). Two types of AAs, l-lysine (Lys) and l-phenylalanine (PhA), were selected to study their effects on loading capacity, release profile of CUR, biocompatibility, and anticancer activity. CUR-loaded AAs-modified IONPs (F@AAs@CUR NPs) were characterized by X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), vibrating sample magnetometer (VSM), and transmission electron microscopy (TEM) techniques. Next, the various kinetic equations were fitted to the release data of CUR from F@Lys@CUR NPs and F@PhA@CUR NPs. Additionally, hemolysis test and MTT assays on HFF-2 and HEK-293 cell lines were performed for determination of biocompatibility of AAs-coated IONPs. Finally, the anticancer activity of F@AAs@CUR NPs examined on MCF-7 breast cancer cell line. The results indicate that these nanocarriers are nontoxic and biocompatible and also F@AAs@CUR NPs are suitable carriers for delivery of curcumin and even other hydrophobic drugs. Also, the MRI training established the effectiveness of IONPs as contrast agent for the revealing of tumor as evidenced from the phantom images as well as higher T2 relaxivity. © 2018 Informa UK Limited, trading as Taylor & Francis Group
dc.language.isoEnglish
dc.relation.ispartofDrug Development and Industrial Pharmacy
dc.titleTheranostic nanoparticles based on magnetic nanoparticles: design, preparation, characterization, and evaluation as novel anticancer drug carrier and MRI contrast agent
dc.typeArticle
dc.citation.spage1
dc.citation.epage11
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1080/03639045.2018.1483398


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