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Multimodal imaging-guided, dual-targeted photothermal therapy for cancer.

Abstract
The ability to selectively destroy cancer cells while sparing normal tissue is highly desirable during cancer therapy. Herein, dual-targeted photothermal therapy was achieved by the integration of upconversion nanoparticles, Fe3O4 nanoparticles (IONPs), Prussian blue nanoparticles (PBNPs) and hyaluronic acid (HA). PBNPs converted near-infrared (NIR) light into heat and HA/Fe3O4 NPs served as dual-targeting moieties. The as-obtained nanocomposites could also be applied as a multimodal probe for upconversion luminescence (UCL) imaging, enhanced T2-weighted magnetic resonance (MR) imaging and photoacoustic tomography (PAT) imaging. This multifunctional nanoparticle (MFNP) system prepared by a layer-by-layer (LBL) assembly method exhibited excellent dispersivity and low toxicity in vitro and in vivo. Furthermore, the research provided effective results for dual-targeted photothermal ablation of cancer with ∼4 fold higher tumor accumulation than that in the absence of HA/magnetic field. The photothermal therapeutic efficacy has been greatly improved in the S180 tumor model. We present a strategy for multimodal imaging-guided, dual-targeted physical cancer therapy and highlight the promise of using multifunctional nanostructures for cancer theranostics.
AuthorsBin Du , Xiaohui Cao , Feifei Zhao , Xiangjie Su , Yuhui Wang , Xiaosa Yan , Shaona Jia , Jie Zhou , Hanchun Yao
JournalJournal of materials chemistry. B (J Mater Chem B) Vol. 4 Issue 11 Pg. 2038-2050 (Mar 21 2016) ISSN: 2050-7518 [Electronic] England
PMID32263081 (Publication Type: Journal Article)

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