Faculty of Engineering, University of Nottingham, Nottingham, UK.
Wolfson STEM Centre, School of Medicine, University of Nottingham, Nottingham, UK.
J Tissue Eng Regen Med. 2019 Mar;13(3):396-405. doi: 10.1002/term.2796. Epub 2019 Feb 17.
Phosphate-based glasses (PBGs) are ideal materials for regenerative medicine strategies because their composition, degradation rates, and ion release profiles can easily be controlled. Strontium has previously been found to simultaneously affect bone resorption and deposition. Therefore, by combining the inherent properties of resorbable PBG and therapeutic activity of strontium, these glasses could be used as a delivery device of therapeutic factors for the treatment of orthopaedic diseases such as osteoporosis. This study shows the cytocompatibility and osteogenic potential of PBGs where CaO is gradually replaced by SrO in the near invert glass system 40P O ·(16-x)CaO·20Na O·24MgO·xSrO (x = 0, 4, 8, 12, and 16 mol%). Direct seeding of MG63 cells onto glass discs showed no significant difference in cell metabolic activity and DNA amount measurement across the different formulations studied. Cell attachment and spreading was confirmed via scanning electron microscopy (SEM) imaging at Days 3 and 14. Alkaline phosphatase (ALP) activity was similarly maintained across the glass compositions. Follow-on studies explored the effect of each glass composition in microsphere conformation (size: 63-125 μm) on human mesenchymal stem cells (hMSCs) in 3D cultures, and analysis of cell metabolic activity and ALP activity showed no significant differences at Day 14 over the compositional range investigated, in line with the observations from MG63 cell culture studies. Environmental SEM and live cell imaging at Day 14 of hMSCs seeded on the microspheres showed cell attachment and colonisation of the microsphere surfaces, confirming these formulations as promising candidates for regenerative medicine strategies addressing compromised musculoskeletal/orthopaedic diseases.
基于磷酸盐的玻璃(PBGs)是再生医学策略的理想材料,因为它们的组成、降解速率和离子释放曲线可以很容易地得到控制。此前已经发现锶同时影响骨吸收和沉积。因此,通过结合可吸收 PBG 的固有特性和锶的治疗活性,这些玻璃可以用作治疗因子的输送装置,用于治疗骨质疏松症等骨科疾病。本研究展示了 PBG 的细胞相容性和成骨潜力,在近反转玻璃系统 40P O·(16-x)CaO·20Na O·24MgO·xSrO(x=0、4、8、12 和 16 mol%)中,CaO 逐渐被 SrO 取代。将 MG63 细胞直接接种到玻璃片上,在不同配方的研究中,细胞代谢活性和 DNA 量的测量没有明显差异。通过扫描电子显微镜(SEM)成像在第 3 天和第 14 天确认细胞附着和铺展。碱性磷酸酶(ALP)活性在玻璃组成物中也得到了维持。后续研究探索了每种玻璃成分在微球形态(大小:63-125 μm)对 3D 培养中的人间充质干细胞(hMSCs)的影响,在研究的组成范围内,细胞代谢活性和 ALP 活性的分析在第 14 天没有显示出显著差异,与 MG63 细胞培养研究的观察结果一致。在接种微球的 hMSCs 上进行环境 SEM 和活细胞成像的第 14 天显示细胞附着和微球表面的定植,证实这些配方是治疗受损的肌肉骨骼/骨科疾病的再生医学策略的有前途的候选物。