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首页> 外文期刊>Acta biomaterialia >Guiding mesenchymal stem cell differentiation using mesoporous silica nanoparticle-based films
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Guiding mesenchymal stem cell differentiation using mesoporous silica nanoparticle-based films

机译:使用介孔二氧化硅纳米粒子基薄膜引导间充质干细胞分化

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The development of smart interfaces that can guide tissue formation is of great importance in the field of regenerative medicine. Nanoparticles represent an interesting class of materials that can be used to enhance regenerative treatments by enabling close control over surface properties and directing cellular responses. Moreover, nanoparticles can be used to provide temporally controlled delivery of (multiple) biochemical compounds. Here, we exploited the cargo loading and surface functionalization properties of mesoporous silica nanoparticles (MSNs) to design films that can guide human mesenchymal stem cell (hMSC) differentiation towards the osteogenic lineage. We developed biocompatible MSN-based films that support stem cell adhesion and proliferation and demonstrated that these MSN films simultaneously allowed efficient local delivery of biomolecules without effecting film integrity. Films loaded with the osteogenesis-stimulating drug dexamethasone (Dex) were able to induce osteogenic differentiation of hMSCs in vitro. Dex delivery from the films led to increased alkaline phosphatase levels and matrix mineralization compared to directly supplementing Dex to the medium. Furthermore, we demonstrated that Dex release kinetics can be modulated using surface modifications with supported lipid bilayers. Together, these data demonstrate that MSN films represent an interesting approach to create biomaterial interfaces with controllable biomolecule release and surface properties to improve the bioactivity of biomaterials.
机译:可以引导组织形成的智能界面的发展在再生医学领域具有重要意义。纳米颗粒代表一种有趣的类别,可用于通过能够在表面性质上紧密控制并引导细胞反应来增强再生处理。此外,纳米颗粒可用于提供(多种)生物化学化合物的时间上受控递送。这里,我们利用了介孔二氧化硅纳米粒子(MSN)的货物加载和表面官能化性能,以设计薄膜,该薄膜可以将人间充质干细胞(HMSC)分化朝向骨质发生谱系分化。我们开发了基于生物相容性的MSN薄膜,其支持干细胞粘附和增殖,并证明这些MSN薄膜同时允许有效地递送生物分子,而不会影响薄膜完整性。装载与促骨发生的刺激药物地塞米松(DEX)的薄膜能够在体外诱导HMSCs的成骨分化。与直接补充培养基相比,从薄膜的DEX递送导致碱性磷酸酶水平和基质矿化增加。此外,我们证明了DEX释放动力学可以使用具有支撑的脂质双层的表面改性来调节。这些数据在一起表明MSN薄膜代表了一种有趣的方法,以产生具有可控生物分子释放和表面性质的生物材料界面,以改善生物材料的生物活性。

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