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A new and facile method to prepare uniform hollow MnO/functionalized mSiO₂ core/shell nanocomposites. | LitMetric

AI Article Synopsis

  • A new type of nanoparticle has been created, featuring a manganese core and a silica shell, designed for improved MRI and photodynamic therapy applications.
  • The etching process used to form hollow versions of these nanoparticles enhances their T(1) signal and allows for better water flow and oxygen diffusion, increasing both imaging capabilities and therapeutic effectiveness.
  • The resulting nanocomposite not only excels in magnetic resonance imaging but also offers optical imaging and promotes cell death, showcasing its multifunctional potential.

Article Abstract

Trifunctional uniform nanoparticles comprising a manganese nanocrystal core and a functionalized mesoporous silica shell (MnO@mSiO(2)(Ir)@PEG, where Ir is an emissive iridium complex and PEG is polyethylene glycol) have been strategically designed and synthesized. The T(1) signal can be optimized by forming hollow core (H-MnO@mSiO(2)(Ir)@PEG) via a novel and facile etching process, for which the mechanism has been discussed in detail. Systematic investigation on correlation for longitudinal relaxation (T(1)) versus core shapes and shell silica porosity of the nanocomposites (MnO, H-MnO, MnO@SiO(2), MnO@mSiO(2), H-MnO@mSiO(2)) has been carried out. The results show that the worm-like nanochannels in the mesoporous silica shell not only increase water permeability to the interior hollow manganese oxide core for T(1) signal but also enhance photodynamic therapy (PDT) efficacy by enabling the free diffusion of oxygen. Notably, the H-MnO@mSiO(2)(Ir)@PEG nanocomposite with promising r(1) relaxivity demonstrates its versatility, in which the magnetic core provides the capability for magnetic resonance imaging, while the simultaneous red phosphorescence and singlet oxygen generation from the Ir complex are capable of providing optical imaging and inducing apoptosis, respectively.

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Source
http://dx.doi.org/10.1021/nn200928rDOI Listing

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