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      Surface functionalized hollow manganese oxide nanoparticles for cancer targeted siRNA delivery and magnetic resonance imaging.

      Biomaterials
      Antibodies, Monoclonal, pharmacology, Antibodies, Monoclonal, Humanized, Cell Line, Tumor, Dihydroxyphenylalanine, Drug Carriers, Electrophoresis, Agar Gel, Gene Silencing, drug effects, Gene Transfer Techniques, Humans, Intracellular Space, metabolism, Magnetic Resonance Imaging, Manganese Compounds, chemistry, Microscopy, Confocal, Nanoparticles, ultrastructure, Neoplasms, pathology, Oxides, Polyethyleneimine, RNA, Small Interfering, Spectroscopy, Fourier Transform Infrared, Surface Properties

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          Abstract

          Multifunctional hollow manganese oxide nanoparticles (HMON) were produced by a bio-inspired surface functionalization approach, using 3,4-dihydroxy-L-phenylalanine (DOPA) as an adhesive moiety, for cancer targeted delivery of therapeutic siRNA and simultaneous diagnosis via magnetic resonance imaging (MRI). Cationic polyethylenimine-DOPA conjugates were stably immobilized onto the surface of HMON due to the strong binding affinity of DOPA to metal oxides, as examined by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. These nanoparticles were subsequently functionalized with a therapeutic monoclonal antibody, Herceptin, to selectively target cancer cells. Confocal microscopy and MR imaging studies revealed that the surface functionalized HMON enabled the targeted detection of cancer cells in T(1)-weighted MRI as well as the efficient intracellular delivery of siRNA for cell-specific gene silencing. These nanomaterials are expected to be widely exploited as multifunctional delivery vehicles for cancer therapy and imaging applications. Copyright © 2010 Elsevier Ltd. All rights reserved.

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