Wang Dan, Lin Huiming, Jiang Jingjie, Han Xiao, Guo Wei, Wu Xiaodan, Jin Yingxue, Qu Fengyu
State Key Laboratory of Photoelectric Band Gap Materials, College of Chemistry and Chemical Engineering, Harbin Normal University, Harbin, People's Republic of China.
Sci Technol Adv Mater. 2013 Apr 19;14(2):025004. doi: 10.1088/1468-6996/14/2/025004. eCollection 2013 Apr.
Magnetic and macro/mesoporous bioactive glasses were synthesized by a one-pot method via a handy salt leaching technique. It was identified to be an effective and simple synthetic strategy. The non-ionic triblock copolymer, poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol) (P123), was used as the structure directing agent for mesoporous structure but also as the reductant to reduce the iron source into magnetic iron oxide. The prepared materials exhibited excellent super-paramagnetic property with interconnected macroporous (200-300 m) and mesoporous (3.4 nm) structure. Furthermore, their outstanding drug storage/release properties and rapid (5) induction of hydroxyapatite growth ability were investigated after immersing in simulated body fluid solution at 37 °C. Notably, the biocompatibility assessment confirmed that the materials obtained presented good biocompatibility and enhanced adherence of HeLa cells. Herein, the novel materials are expected to have potential application for bone tissue engineering.
通过简便的盐浸技术采用一锅法合成了磁性和大孔/介孔生物活性玻璃。它被确定为一种有效且简单的合成策略。非离子三嵌段共聚物聚(乙二醇)-嵌段-聚(丙二醇)-嵌段-聚(乙二醇)(P123)用作介孔结构的结构导向剂,同时也用作将铁源还原为磁性氧化铁的还原剂。所制备的材料表现出优异的超顺磁性,具有相互连接的大孔(200 - 300μm)和介孔(3.4nm)结构。此外,在37°C下浸泡于模拟体液溶液后,研究了它们出色的药物储存/释放性能和快速(5天)诱导羟基磷灰石生长的能力。值得注意的是,生物相容性评估证实所获得的材料具有良好的生物相容性,并增强了HeLa细胞的黏附。在此,预期这些新型材料在骨组织工程中具有潜在应用。