| Literature DB >> 29266514 |
Jung-Tak Jang1, Jooyoung Lee2, Jiyun Seon1, Eric Ju1, Minkyu Kim2, Young Il Kim3, Min Gyu Kim4, Yasushi Takemura5, Ali Syed Arbab6, Keon Wook Kang7, Ki Ho Park8, Sun Ha Paek2, Seongtae Bae1.
Abstract
Magnetic fluid hyperthermia has been recently considered as a Renaissance of cancer treatment modality due to its remarkably low side effects and high treatment efficacy compared to conventional chemotheraphy or radiotheraphy. However, insufficient AC induction heating power at a biological safe range of AC magnetic field (Happl ·fappl < 3.0-5.0 × 109 A m-1 s-1 ), and highly required biocompatibility of superparamagnetic nanoparticle (SPNP) hyperthermia agents are still remained as critical challenges for successful clinical hyperthermia applications. Here, newly developed highly biocompatible magnesium shallow doped γ-Fe2 O3 (Mg0.13 -γFe2 O3 ) SPNPs with exceptionally high intrinsic loss power (ILP) in a range of 14 nH m2 kg-1 , which is an ≈100 times higher than that of commercial Fe3 O4 (Feridex, ILP = 0.15 nH m2 kg-1 ) at Happl ·fappl = 1.23 × 109 A m-1 s-1 are reported. The significantly enhanced heat induction characteristics of Mg0.13 -γFe2 O3 are primarily due to the dramatically enhanced out-of-phase magnetic susceptibility and magnetically tailored AC/DC magnetic softness resulted from the systematically controlled Mg2+ cations distribution and concentrations in octahedral site Fe vacancies of γ-Fe2 O3 instead of well-known Fe3 O4 SPNPs. In vitro and in vivo magnetic hyperthermia studies using Mg0.13 -γFe2 O3 nanofluids are conducted to estimate bioavailability and biofeasibility. Mg0.13 -γFe2 O3 nanofluids show promising hyperthermia effects to completely kill the tumors.Entities:
Keywords: Mg-doped γ-Fe2O3 nanoparticles; cancer treatment; giant magnetic heat induction; intrinsic loss power; magnetic fluid hyperthermia
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Year: 2017 PMID: 29266514 DOI: 10.1002/adma.201704362
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849