Díaz Esperanza, Blanca Valle M Lt Sup Gt A Lt/Sup Gt, Ribeiro Sylvie, Lanceros-Mendez Senentxu, Barandiarán José Manuel
Escuela de Ingeniería de Bilbao, Departamento de Ingeniería Minera, Metalúrgica y Ciencia de Materiales, Universidad del País Vasco (UPV/EHU), 48920 Portugalete, Spain.
BCMaterials, Basque Centre for Materials, Applications and Nanostructures, UPV/EHU Science Park, 48940 Leioa, Spain.
Materials (Basel). 2019 Nov 21;12(23):3843. doi: 10.3390/ma12233843.
A study of Magnetite (FeO) as a suitable matrix for the improved adhesion and proliferation of MC3T3-E1 pre-osteoblast cells in bone regeneration is presented. Biodegradable and magnetic polycaprolactone (PCL)/magnetite (FeO) scaffolds, which were fabricated by Thermally Induced Phase Separation, are likewise analyzed. Various techniques are used to investigate in vitro degradation at 37 °C, over 104 weeks, in a phosphate buffered saline (PBS) solution. Magnetic measurements that were performed at physiological temperature (310 K) indicated that degradation neither modified the nature nor the distribution of the magnetite nanoparticles. The coercive field strength of the porous matrices demonstrated ferromagnetic behavior and the probable presence of particle interactions. The added nanoparticles facilitated the absorption of PBS, with no considerable increase in matrix degradation rates, as shown by the Gel Permeation Chromatography (GPC) results for Mw, Mn, and I. There was no collapse of the scaffold structures that maintained their structural integrity. Their suitability for bone regeneration was also supported by the absence of matrix cytotoxicity in assays, even after additions of up to 20% magnetite.
本文介绍了一项关于磁铁矿(FeO)作为改善MC3T3-E1前成骨细胞在骨再生中黏附与增殖的合适基质的研究。同时也分析了通过热致相分离法制备的可生物降解磁性聚己内酯(PCL)/磁铁矿(FeO)支架。采用多种技术研究了在37℃下于磷酸盐缓冲盐水(PBS)溶液中长达104周的体外降解情况。在生理温度(310K)下进行的磁性测量表明,降解既未改变磁铁矿纳米颗粒的性质,也未改变其分布。多孔基质的矫顽场强度表现出铁磁行为以及可能存在的颗粒相互作用。如凝胶渗透色谱(GPC)对Mw、Mn和I的结果所示,添加的纳米颗粒促进了PBS的吸收,而基质降解速率没有显著增加。支架结构没有坍塌,保持了其结构完整性。即使添加高达20%的磁铁矿,在试验中也未出现基质细胞毒性,这也支持了它们适用于骨再生。
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