Zhou Xiaojun, Qian Yuhan, Chen Liang, Li Tao, Sun Xin, Ma Xiaojun, Wang Jinwu, He Chuanglong
State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Shanghai Engineering Research Center of Nano-Biomaterials and Regenerative Medicine, College of Biological Science and Medical Engineering, Donghua University, Shanghai 201620, China.
Department of Joint Surgery, Zhongshan Hospital of Traditional Chinese Medicine Affiliated to Guangzhou University of Traditional Chinese Medicine, Zhongshan 528400, China.
ACS Nano. 2023 Mar 14;17(5):5140-5156. doi: 10.1021/acsnano.3c00598. Epub 2023 Feb 21.
The favorable microstructure and bioactivity of tissue-engineered bone scaffolds are closely associated with the regenerative efficacy of bone defects. For the treatment of large bone defects, however, most of them fail to meet requirements such as adequate mechanical strength, highly porous structure, and excellent angiogenic and osteogenic activities. Herein, inspired by the characteristics of a "flowerbed", we construct a short nanofiber aggregates-enriched dual-factor delivery scaffold 3D printing and electrospinning techniques for guiding vascularized bone regeneration. By the assembly of short nanofibers containing dimethyloxalylglycine (DMOG)-loaded mesoporous silica nanoparticles with a 3D printed strontium-contained hydroxyapatite/polycaprolactone (SrHA@PCL) scaffold, an adjustable porous structure can be easily realized by changing the density of nanofibers, while strong compressive strength will be acquired due to the framework role of SrHA@PCL. Owing to the different degradation performance between electrospun nanofibers and 3D printed microfilaments, a sequential release behavior of DMOG and Sr ions is achieved. Both and results demonstrate that the dual-factor delivery scaffold has excellent biocompatibility, significantly promotes angiogenesis and osteogenesis by stimulating endothelial cells and osteoblasts, and effectively accelerates tissue ingrowth and vascularized bone regeneration through activating the hypoxia inducible factor-1α pathway and immunoregulatory effect. Overall, this study has provided a promising strategy for constructing a bone microenvironment-matched biomimetic scaffold for bone regeneration.
组织工程骨支架良好的微观结构和生物活性与骨缺损的再生效果密切相关。然而,对于大骨缺损的治疗,大多数支架未能满足诸如足够的机械强度、高度多孔结构以及优异的血管生成和成骨活性等要求。在此,受“花坛”特征的启发,我们采用3D打印和静电纺丝技术构建了一种富含短纳米纤维聚集体的双因子递送支架,用于引导血管化骨再生。通过将负载二甲基草酰甘氨酸(DMOG)的介孔二氧化硅纳米颗粒的短纳米纤维与3D打印的含锶羟基磷灰石/聚己内酯(SrHA@PCL)支架组装在一起,通过改变纳米纤维的密度可以轻松实现可调节的多孔结构,同时由于SrHA@PCL的骨架作用将获得较强的抗压强度。由于静电纺纳米纤维和3D打印微丝之间不同的降解性能,实现了DMOG和锶离子的顺序释放行为。体外和体内结果均表明,双因子递送支架具有优异的生物相容性,通过刺激内皮细胞和成骨细胞显著促进血管生成和成骨,并通过激活缺氧诱导因子-1α途径和免疫调节作用有效加速组织长入和血管化骨再生。总体而言,本研究为构建与骨微环境匹配的用于骨再生的仿生支架提供了一种有前景的策略。