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      Synthesis of Ferromagnetic Fe0.6Mn0.4O Nanoflowers as a New Class of Magnetic Theranostic Platform for In Vivo T1-T2Dual-Mode Magnetic Resonance Imaging and Magnetic Hyperthermia Therapy

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          Abstract

          Uniform wüstite Fe0.6 Mn0.4 O nanoflowers have been successfully developed as an innovative theranostic agent with T1 -T2 dual-mode magnetic resonance imaging (MRI), for diagnostic applications and therapeutic interventions via magnetic hyperthermia. Unlike their antiferromagnetic bulk counterpart, the obtained Fe0.6 Mn0.4 O nanoflowers show unique room-temperature ferromagnetic behavior, probably due to the presence of an exchange coupling effect. Combined with the flower-like morphology, ferromagnetic Fe0.6 Mn0.4 O nanoflowers are demonstrated to possess dual-modal MRI sensitivity, with longitudinal relaxivity r1 and transverse relaxivity r2 as high as 4.9 and 61.2 mm(-1) s(-1) [Fe]+[Mn], respectively. Further in vivo MRI carried out on the mouse orthotopic glioma model revealed gliomas are clearly delineated in both T1 - and T2 -weighted MR images, after administration of the Fe0.6 Mn0.4 O nanoflowers. In addition, the Fe0.6 Mn0.4 O nanoflowers also exhibit excellent magnetic induction heating effects. Both in vitro and in vivo magnetic hyperthermia experimentation has demonstrated that magnetic hyperthermia by using the innovative Fe0.6 Mn0.4 O nanoflowers can induce MCF-7 breast cancer cell apoptosis and a complete tumor regression without appreciable side effects. The results have demonstrated that the innovative Fe0.6 Mn0.4 O nanoflowers can be a new magnetic theranostic platform for in vivo T1 -T2 dual-mode MRI and magnetic thermotherapy, thereby achieving a one-stop diagnosis cum effective therapeutic modality in cancer management.

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            Magnetic nanomaterials for hyperthermia-based therapy and controlled drug delivery.

            Previous attempts to review the literature on magnetic nanomaterials for hyperthermia-based therapy focused primarily on magnetic fluid hyperthermia (MFH) using mono metallic/metal oxide nanoparticles. The term "hyperthermia" in the literature was also confined only to include use of heat for therapeutic applications. Recently, there have been a number of publications demonstrating magnetic nanoparticle-based hyperthermia to generate local heat resulting in the release of drugs either bound to the magnetic nanoparticle or encapsulated within polymeric matrices. In this review article, we present a case for broadening the meaning of the term "hyperthermia" by including thermotherapy as well as magnetically modulated controlled drug delivery. We provide a classification for controlled drug delivery using hyperthermia: Hyperthermia-based controlled drug delivery through bond breaking (DBB) and hyperthermia-based controlled drug delivery through enhanced permeability (DEP). The review also covers, for the first time, core-shell type magnetic nanomaterials, especially nanoshells prepared using layer-by-layer self-assembly, for the application of hyperthermia-based therapy and controlled drug delivery. The highlight of the review article is to portray potential opportunities for the combination of hyperthermia-based therapy and controlled drug release paradigms--towards successful application in personalized medicine. Copyright © 2011 Elsevier B.V. All rights reserved.
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              Exchange-coupled magnetic nanoparticles for efficient heat induction.

              The conversion of electromagnetic energy into heat by nanoparticles has the potential to be a powerful, non-invasive technique for biotechnology applications such as drug release, disease treatment and remote control of single cell functions, but poor conversion efficiencies have hindered practical applications so far. In this Letter, we demonstrate a significant increase in the efficiency of magnetic thermal induction by nanoparticles. We take advantage of the exchange coupling between a magnetically hard core and magnetically soft shell to tune the magnetic properties of the nanoparticle and maximize the specific loss power, which is a gauge of the conversion efficiency. The optimized core-shell magnetic nanoparticles have specific loss power values that are an order of magnitude larger than conventional iron-oxide nanoparticles. We also perform an antitumour study in mice, and find that the therapeutic efficacy of these nanoparticles is superior to that of a common anticancer drug.
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                Author and article information

                Journal
                Advanced Healthcare Materials
                Adv. Healthcare Mater.
                Wiley
                21922640
                August 2016
                August 2016
                June 14 2016
                : 5
                : 16
                : 2092-2104
                Affiliations
                [1 ]Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education; College of Chemistry and Materials Science; Northwest University; Xi'an 710069 China
                [2 ]Department of Materials Science and Engineering; Faculty of Engineering; National University of Singapore; 7 Engineering Drive 1 117574 Singapore
                [3 ]Department of Anatomy; Yong Loo Lin School of Medicine; National University of Singapore 4 Medical Drive; MD10 117597 Singapore
                [4 ]Magnetic Resonance Imaging Group; Singapore Bioimaging Consortium; Agency for Science Technology and Research (A*STAR); 11 Biopolis Way, #02-02 Helios 138667 Singapore
                [5 ]State Key Laboratory of Magnetism and Beijing National Laboratory for Condensed Matter Physics; Chinese Academy of Sciences; Beijing 100190 China
                [6 ]Key Laboratory of Advanced Materials; Ministry of Education; School of Material Science and Engineering; Tsinghua University; Beijing 100084 China
                [7 ]NUS Graduate School for Integrative Sciences and Engineering; National University of Singapore; 28 Medical Drive 117456 Singapore
                [8 ]School of Materials Science and Engineering; University of New South Wales; Kensington NSW 2052 Australia
                Article
                10.1002/adhm.201600357
                27297640
                a1749094-7c2c-497d-bdf9-7a81553b779d
                © 2016

                http://doi.wiley.com/10.1002/tdm_license_1.1

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