Biomaterials Research Group, Department of Materials Engineering, Isfahan University of Technology, Isfahan, 84156-83111, Iran.
Department of Cellular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
J Biomed Mater Res A. 2019 Jul;107(7):1358-1365. doi: 10.1002/jbm.a.36649. Epub 2019 Feb 23.
In this study, submicron, monodispersed, spherical bioactive glass (BG) particles with a mean diameter of 720 ± 80 nm were produced through sol-gel process. The prepared BG particles were successfully incorporated into 70/30 (W/W) ratio of polycaprolactone/gelatin (PCL/GT) nanofibrous mats (250 ± 60 nm) through electrospinning to obtain a unique architectural structure for the first time. To enhance biodegradation and stability of the scaffolds, crosslinking using gluteraldehyde was applied. The structure, wettability, hydroxyapatite (HA) formation, cell adhesion, cell viability and osteogenic potential of the fibrous mats were evaluated. A continuous, uniform and hydrophilic structure of PCL/GT/BG was obtained. The fibers were found to be bioactive as they formed HA on their surface after immersion in simulated body fluid. The unique structure significantly reduced HA formation time to 5 days. For in vitro investigations, human dental pulp stem cells (hDPSCs) were cultured on PCL/GT and PCL/GT/BG fibrous mats. Results demonstrated good cell attachment after 4 and 24 h with no significant levels of cytotoxicity during 10 days of culture. Alizarin red staining was applied to quantitatively analyze the potential of PCL/GT/BG in osteogenic differentiation of hDPSCs. © 2019 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2019.
在这项研究中,通过溶胶-凝胶工艺制备了平均直径为 720±80nm 的亚微米、单分散、球形生物活性玻璃(BG)颗粒。通过静电纺丝,成功地将制备的 BG 颗粒掺入到聚己内酯/明胶(PCL/GT)纳米纤维垫中,其质量比为 70/30(W/W)(250±60nm),首次获得了独特的建筑结构。为了提高支架的生物降解性和稳定性,使用戊二醛进行交联。评估了纤维垫的结构、润湿性、羟基磷灰石(HA)形成、细胞黏附、细胞活力和成骨潜力。获得了具有连续、均匀和亲水性结构的 PCL/GT/BG。纤维被发现具有生物活性,因为它们在浸入模拟体液后在其表面形成了 HA。独特的结构将 HA 的形成时间显著缩短至 5 天。在体外研究中,将人牙髓干细胞(hDPSCs)培养在 PCL/GT 和 PCL/GT/BG 纤维垫上。结果表明,培养 4 和 24 小时后细胞附着良好,在 10 天的培养过程中没有明显的细胞毒性。茜素红染色定量分析了 PCL/GT/BG 促进 hDPSCs 成骨分化的潜力。© 2019 约翰威立父子公司。J 生物医学材料研究 A 部分,2019 年。