Yadav Akhilesh Kumar, Kumar Satish, Rajput Sanjna, Das Nilesh Kumar, Goswami Chandan, Rath Chandana
School of Materials Science and Technology, Indian Institute of Technology (Banaras Hindu University), Varanasi 221005, India.
School of Biological Sciences, National Institute of Science Education and Research, HBNI, Jatni 752050, Odisha, India.
Int J Biol Macromol. 2025 Sep;321(Pt 1):146283. doi: 10.1016/j.ijbiomac.2025.146283. Epub 2025 Jul 23.
Current bio-medical situation necessitates the development of natural and/or synthetic biomaterials that can enhance biomineralization both in-vitro and in-vivo. Towards that aim, we synthesized nanofibrous scaffolds of 81S(81SiO₂-12CaO-2P₂O₅-1Na₂O-4MgO) and 85S(85SiO₂-10CaO-5P₂O₅ mol%) bio-glass of varying concentrations with gelatin using electrospinning. XRD and FTIR confirm scaffold formation, while SEM-EDS analysis reveals fibrous structure with homogenous distribution of nBG inside the fibre. All scaffolds are found to be hydrophilic. MTT assay reveals non-cytotoxicity towards Saos-2 cells for all the scaffolds. Further, biocompatibility studies using DAPI, Phalloidin, and Vinculin show enhanced adhesion and proliferation of osteogenic cells using 85S_5 scaffolds. Cellular ROS levels (via HDCFDA) remain unchanged, though mitochondrial ROS (via MitoSOX) increases in 85S_5 and decreases in 85S_10. Both 85S_5 and 85S_10 scaffolds exhibit increased mitochondrial membrane potential (∆Ψm) measured by TMRM. These scaffolds enhance the metabolic status of mitochondria, which is critical for osteogenesis. Besides, no significant change in cardiolipin levels is observed. ALP assay confirms early osteogenic differentiation, and mineralization assay shows significant calcium-based nodule deposition for both scaffolds. The study suggests that the synthesized 85S_5 scaffold is non-toxic and non-detrimental towards the osteogenic cells, supports adhesion, proliferation and differentiation, thus can serve as suitable scaffold for repair/regeneration of bone tissue.
当前的生物医学状况需要开发能够在体外和体内增强生物矿化的天然和/或合成生物材料。为了实现这一目标,我们使用静电纺丝技术,将不同浓度的81S(81SiO₂-12CaO-2P₂O₅-1Na₂O-4MgO)和85S(85SiO₂-10CaO-5P₂O₅摩尔%)生物玻璃与明胶合成了纳米纤维支架。XRD和FTIR证实了支架的形成,而SEM-EDS分析揭示了纤维结构以及nBG在纤维内的均匀分布。所有支架均具有亲水性。MTT试验表明所有支架对Saos-2细胞均无细胞毒性。此外,使用DAPI、鬼笔环肽和纽蛋白进行的生物相容性研究表明,85S_5支架可增强成骨细胞的粘附和增殖。细胞ROS水平(通过HDCFDA检测)保持不变,尽管85S_5中通过MitoSOX检测的线粒体ROS增加,而85S_10中则减少。85S_5和85S_10支架均表现出通过TMRM测量的线粒体膜电位(∆Ψm)增加。这些支架增强了线粒体的代谢状态,这对骨生成至关重要。此外,未观察到心磷脂水平有显著变化。ALP试验证实了早期成骨分化,矿化试验表明两种支架均有显著的钙基结节沉积。该研究表明,合成的85S_5支架对成骨细胞无毒且无害,支持粘附、增殖和分化,因此可作为骨组织修复/再生的合适支架。