Yuan Zuoying, Wan Zhuo, Wei Pengfei, Lu Xin, Mao Jianping, Cai Qing, Zhang Xu, Yang Xiaoping
State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.
Beijing Laboratory of Biomedical Materials, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.
Adv Healthc Mater. 2020 Jun;9(11):e2000211. doi: 10.1002/adhm.202000211. Epub 2020 Apr 27.
Current scaffolds applied for bone tissue engineering are still lacking sufficient osteogenic capacity to induce efficient bone regeneration. Biodegradable microsphere-type scaffolds are designed to achieve the dual-controlled release of a Chinese medicine (i.e., icariin, ICA) and a bioactive ion (i.e., Mg ), in order to achieve their synergistic effect on inducing osteogenesis. The hydrophobic icariin is preloaded onto MgO/MgCO (1:1 in weight ratio) particles at different amounts and then the particles are encapsulated into biodegradable poly(lactide-co-glycolide) (PLGA) microspheres (PMI) at a fixed fraction (20 wt%). Continuous releases of Mg ion and icariin from the microspheres are detected, showing dependence on icariin amounts. At an optimized moderate loading amount, the resulting PMI-M microspheres display the strongest activation effect on cell biological behaviors among all the designs. By implanting the PMI-M microspheres into rat calvarial defects for 16 weeks, it is found that they can effectively enhance new bone formation, presenting significantly higher capacity in inducing osteogenesis than PMg (containing MgO/MgCO but without icariin) and blank PLGA microspheres. Clearly, the released Mg ions are beneficial to osteogenesis, and the coincorporation of icariin exerts supplemental effects in inducing new bone formation, which suggest a promising strategy to regenerate severe bone injuries by designing a dual-release system.
目前应用于骨组织工程的支架仍缺乏足够的成骨能力来诱导有效的骨再生。可生物降解的微球型支架被设计用于实现一种中药(即淫羊藿苷,ICA)和一种生物活性离子(即Mg)的双重控释,以实现它们在诱导成骨方面的协同作用。将疏水性的淫羊藿苷以不同量预先负载到MgO/MgCO(重量比为1:1)颗粒上,然后将这些颗粒以固定比例(20 wt%)封装到可生物降解的聚(丙交酯-共-乙交酯)(PLGA)微球(PMI)中。检测到微球中Mg离子和淫羊藿苷的持续释放,显示出对淫羊藿苷量的依赖性。在优化的适度负载量下,所得的PMI-M微球在所有设计中对细胞生物学行为表现出最强的激活作用。通过将PMI-M微球植入大鼠颅骨缺损处16周,发现它们可以有效地促进新骨形成,在诱导成骨方面表现出比PMg(含有MgO/MgCO但不含淫羊藿苷)和空白PLGA微球显著更高的能力。显然,释放的Mg离子有利于成骨,淫羊藿苷的共同掺入在诱导新骨形成方面发挥补充作用,这表明通过设计双重释放系统来再生严重骨损伤是一种有前景的策略。