AI Article Synopsis

  • Recent advancements in bone cancer treatments have been driven by new biomaterials, particularly in managing small and accessible tumors through surgical removal and scaffolding.
  • A novel heterostructured nanobiomaterial has been developed, featuring a bioactive glass shell and a superparamagnetic iron oxide core, aiming to enhance bone repair and target cancer cells with magnetic hyperthermia.
  • Initial tests show that these core-shell nanoparticles have good heating capacity, rapid mineralization, and cytocompatibility with human stem cells, indicating their potential for effectively repairing bone defects after tumor resections while also aiding in cancer treatment.

Article Abstract

The past few decades have seen the development of new bone cancer therapies, triggered by the discovery of new biomaterials. When the tumoral area is small and accessible, the common clinical treatment implies the tumor mass removal followed by bone reconstruction or consolidation with a bioceramic or a metallic scaffold. Even though the treatment also involves chemotherapy or radiotherapy, resurgence of cancer cells remains possible. We have thus designed a new kind of heterostructured nanobiomaterial, composed of SiO-CaO bioactive glass as the shell and superparamagnetic γ-FeO iron oxide as the core in order to combine the benefits of bone repair thanks to the glass bioactivity and cancer cell destruction through magnetic hyperthermia. These multifunctional core-shell nanoparticles (NPs) have been obtained using a two-stage procedure, involving the coprecipitation of 11 nm sized iron oxide NPs followed by their encapsulation inside a bioactive glass shell by sol-gel chemistry. The as-produced spherical multicore-shell NPs show a narrow size distribution of 73 ± 7 nm. Magnetothermal loss measurements by calorimetry under an alternating magnetic field and in vitro bioactivity assessment performed in simulated body fluid showed that these heterostructures exhibit a good heating capacity and a fast mineralization process (hydroxyapatite forming ability). In addition, their in vitro cytocompatibility, evaluated in the presence of human mesenchymal stem cells during 3 and 7 days, has been demonstrated. These first findings suggest that γ-FeO@SiO-CaO heterostructures are a promising biomaterial to fill bone defects resulting from bone tumor resection, as they have the ability to both repair bone tissue and act as thermoseeds for cancer therapy.

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Source
http://dx.doi.org/10.1021/acsami.0c12769DOI Listing

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