2 research outputs found

    Trifunctional Fe<sub>3</sub>O<sub>4</sub>/CaP/Alginate Core–Shell–Corona Nanoparticles for Magnetically Guided, pH-Responsive, and Chemically Targeted Chemotherapy

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    Chemotherapy of bladder cancer has limited efficacy because of the short retention time of drugs in the bladder during therapy. In this research, nanoparticles (NPs) with a new core/shell/corona nanostructure have been synthesized, consisting of iron oxide (Fe<sub>3</sub>O<sub>4</sub>) as the core to providing magnetic properties, drug (doxorubicin) loaded calcium phosphate (CaP) as the shell for pH-responsive release, and arginylglycylaspartic acid (RGD)-containing peptide functionalized alginate as the corona for cell targeting (with the composite denoted as RGD-Fe<sub>3</sub>O<sub>4</sub>/CaP/Alg NPs). We have optimized the reaction conditions to obtain RGD-Fe<sub>3</sub>O<sub>4</sub>/CaP/Alg NPs with high biocompatibility and suitable particle size, surface functionality, and drug loading/release behavior. The results indicate that the RGD-Fe<sub>3</sub>O<sub>4</sub>/CaP/Alg NPs exhibit enhanced chemotherapy efficacy toward T24 bladder cancer cells, owing to successful magnetic guidance, pH-responsive release, and improved cellular uptake, which give these NPs great potential as therapeutic agents for future in vivo drug delivery systems

    Mesoporous TiO<sub>2</sub> Embedded with a Uniform Distribution of CuO Exhibit Enhanced Charge Separation and Photocatalytic Efficiency

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    Mixed metal oxide nanoparticles have interesting physical and chemical properties, but synthesizing them with colloidal methods is still challenging and often results in very heterogeneous structures. Here, we describe a simple method to synthesize mesoporous titania nanoparticles implanted with a uniform distribution of copper oxide nanocrystals (CuO@MTs). By calcining a titanium-based metal–organic framework (MIL-125) in the presence of Cu ions, we can trap the Cu in the TiO<sub>2</sub> matrix. Removal of the organic ligand creates mesoporosity and limits phase separation so that tiny CuO nanocrystals form in the interstices of the TiO<sub>2</sub>. The CuO@MTs exhibits superior performance for photocatalytic hydrogen evolution (4760 μmol h<sup>–1</sup>) that is >90 times larger than pristine titania
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