CNRS, SIGMA Clermont, ICCF, Université Clermont Auvergne, Clermont-Ferrand F-63000, France.
Institut de Physique et Chimie des Matériaux de Strasbourg (IPCMS), UMR-7504 CNRS-Université de Strasbourg, 23 rue du Lœss, BP 34, Strasbourg 67034 Cedex 2, France.
ACS Appl Mater Interfaces. 2020 Oct 21;12(42):47820-47830. doi: 10.1021/acsami.0c12769. Epub 2020 Oct 8.
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.
在过去的几十年中,由于新型生物材料的发现,新的骨癌疗法不断发展。当肿瘤区域较小时且易于接近,常见的临床治疗方法包括肿瘤切除,然后用生物陶瓷或金属支架进行骨重建或加固。即使治疗还包括化疗或放疗,癌细胞仍有可能复发。因此,我们设计了一种新型的异质结构纳米生物材料,由 SiO-CaO 生物活性玻璃作为外壳和超顺磁 γ-FeO 氧化铁作为核心组成,以结合玻璃生物活性的优势来修复骨骼,并通过磁热疗破坏癌细胞。这些多功能核壳纳米粒子(NPs)是通过两步法获得的,涉及 11nm 大小的氧化铁 NPs 的共沉淀,然后通过溶胶-凝胶化学将其封装在生物活性玻璃壳内。所制备的球形多核壳 NPs 具有 73±7nm 的窄粒径分布。在交变磁场下通过量热法进行的磁热损耗测量和在模拟体液中的体外生物活性评估表明,这些异质结构具有良好的加热能力和快速的矿化过程(形成羟基磷灰石的能力)。此外,还在人骨髓间充质干细胞存在的情况下进行了 3 天和 7 天的体外细胞相容性评估。这些初步发现表明,γ-FeO@SiO-CaO 异质结构是一种有前途的生物材料,可以填充骨肿瘤切除后产生的骨缺损,因为它们既有修复骨组织的能力,又有作为癌症治疗热种子的能力。