Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, 55905, USA; Department of Orthopedic Surgery, Mayo Clinic, Rochester, MN, 55905, USA.
Department of Cardiovascular Diseases and Center for Regenerative Medicine, Mayo Clinic, Rochester, MN, 55905, USA.
Biomaterials. 2021 Sep;276:121014. doi: 10.1016/j.biomaterials.2021.121014. Epub 2021 Jul 6.
Injectable polymers have attracted intensive attention in tissue engineering and drug delivery applications. Current injectable polymer systems often require free-radical or heavy-metal initiators and catalysts for the crosslinking process, which may be extremely toxic to the human body. Here, we report a novel polyhedral oligomeric silsesquioxane (POSS) based strain-promoted alkyne-azide cycloaddition (SPAAC) "click" organic-inorganic nanohybrids (click-ON) system that can be click-crosslinked without any toxic initiators or catalysts. The click-ON scaffolds supported excellent adhesion, proliferation, and osteogenesis of stem cells. In vivo evaluation using a rat cranial defect model showed outstanding bone formation with minimum cytotoxicity. Essential osteogenic alkaline phosphatase (ALP) and vascular CD31 marker expression were detected on the defect site, indicating excellent support of in vivo osteogenesis and vascularization. Using salt leaching techniques, an injectable porous click-ON cement was developed to create porous structures and support better in vivo bone regeneration. Beyond defect filling, the click-ON cement also showed promising application for spinal fusion using rabbits as a model. Compared to the current clinically used poly (methyl methacrylate) (PMMA) cement, this click-ON cement showed great advantages of low heat generation, better biocompatibility and biodegradability, and thus has great potential for bone and related tissue engineering applications.
可注射聚合物在组织工程和药物输送应用中引起了广泛关注。目前的可注射聚合物系统通常需要自由基或重金属引发剂和催化剂来进行交联过程,这可能对人体极其有害。在这里,我们报告了一种新型的基于多面体低聚倍半硅氧烷(POSS)的应变促进炔基-叠氮化物环加成(SPAAC)“点击”有机-无机纳米杂化(click-ON)系统,无需任何有毒引发剂或催化剂即可进行点击交联。click-ON 支架支持干细胞的出色粘附、增殖和成骨作用。使用大鼠颅缺损模型的体内评估显示,具有最小细胞毒性的出色骨形成。在缺陷部位检测到必需的成骨碱性磷酸酶(ALP)和血管 CD31 标志物表达,表明对体内成骨和血管生成的出色支持。通过盐浸出技术,开发了一种可注射多孔 click-ON 水泥,以形成多孔结构并支持更好的体内骨再生。除了缺陷填充外,click-ON 水泥在兔作为模型的脊柱融合中也显示出了有前途的应用。与目前临床使用的聚甲基丙烯酸甲酯(PMMA)水泥相比,这种 click-ON 水泥具有低热生成、更好的生物相容性和生物降解性等优点,因此在骨和相关组织工程应用中具有很大的潜力。