Department of Ceramic Engineering, Indian Institute of Technology (BHU), Varanasi, Uttar Pradesh, India.
Cellular Immunology Laboratory, Department of Zoology, University of Burdwan, Purba Bardhaman, West Bengal, India.
J Biomed Mater Res B Appl Biomater. 2023 May;111(5):1059-1073. doi: 10.1002/jbm.b.35214. Epub 2022 Dec 30.
We developed ZnO-assisted 1393 bioactive glass-based scaffold with suitable mechanical properties through foam replica technique and observed to be suitable for bone tissue engineering application. However, the developed scaffolds' ability to facilitate cellular infiltration and integration was further assessed through in vivo studies in suitable animal model. Herein, the pure 1393 bioactive glass (BG) and ZnO-assisted 1393 bioactive glass- (ZnBGs; 1, 2, 4 mol% ZnO substitution for SiO in pure BG is named as Z1BG, Z2BG, Z3BG, respectively) based scaffolds were prepared through sol-gel route, followed by foam replica techniques and characterized by a series of in vitro and some in vivo tests. Different cell lines like normal mouse embryonic cells (NIH/3T3), mouse bone marrow stromal cells (mBMSc), peripheral blood mononuclear cells, that is, lymphocytes and monocytes (PBMC) and U2OS (carcinogenic human osteosarcoma cells) were used in determination and comparative analysis of the biological compatibility of the BG and ZnBGs. Also, the alkaline phosphatase (ALP) activity, and osteogenic gene expression by primer-specific osteopontin (OPN), osteocalcin (OCN), and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) genes were performed to study osteogenic differentiability of the stromal cells in different BGs. Moreover, radiological and histopathological tests were performed in bone defect model of Wister rats to evaluate the in vivo bone regeneration and healing. Interestingly, these studies demonstrate augmented biological compatibility, and superior osteogenic differentiation in ZnBGs, in particular Z3BG than the pure BG in most cases.
我们通过泡沫复制技术开发了具有合适机械性能的 ZnO 辅助 1393 生物活性玻璃基支架,并观察到其适合骨组织工程应用。然而,通过在合适的动物模型中的体内研究进一步评估了开发的支架促进细胞渗透和整合的能力。在此,通过溶胶-凝胶法制备了纯 1393 生物活性玻璃(BG)和 ZnO 辅助 1393 生物活性玻璃(ZnBG;SiO 中 1、2、4 mol% 的 ZnO 取代分别命名为 Z1BG、Z2BG、Z3BG)基支架,然后通过泡沫复制技术进行了一系列的体外和一些体内测试。不同的细胞系,如正常小鼠胚胎细胞(NIH/3T3)、小鼠骨髓基质细胞(mBMSc)、外周血单核细胞,即淋巴细胞和单核细胞(PBMC)和 U2OS(致癌性人骨肉瘤细胞)用于确定和比较 BG 和 ZnBGs 的生物相容性。此外,通过碱性磷酸酶(ALP)活性和引物特异性骨桥蛋白(OPN)、骨钙素(OCN)和甘油醛-3-磷酸脱氢酶(GAPDH)基因的表达来研究基质细胞在不同 BGs 中的成骨分化能力。此外,在 Wister 大鼠骨缺损模型中进行了放射学和组织病理学测试,以评估体内骨再生和愈合情况。有趣的是,这些研究表明,在大多数情况下,与纯 BG 相比,ZnBGs,特别是 Z3BG 具有增强的生物相容性和更好的成骨分化能力。