Department of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, Guangdong, PR China; Department of Orthopeadics and Traumatology, LKS Faculty of Medicine, the University of Hong Kong, HK SAR, PR China; Department of Orthopeadics and Traumatology, Guangdong Second Provincial General Hospital, Guangzhou 510317, PR China.
Department of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, Guangdong, PR China.
Carbohydr Polym. 2021 Dec 1;273:118532. doi: 10.1016/j.carbpol.2021.118532. Epub 2021 Aug 4.
Bone defects caused by trauma have become increasingly common in aged populations. Clinically, because of the relatively decreased bone healing capacity compared with the youth adults, bone defect repair in the elderly remains challenging. The development of effective biomaterials targeted at bone defects in the elderly is a key component of bone-tissue engineering strategies. However, little attention has been paid to bone regeneration in the elderly. Here, we developed a new scaffold chitosan-Strontium chondroitin sulfate (CH-SrCS) and evaluated its effect on improving bone regeneration. We find that the CH-SrCS scaffold displayed positive effects on downregulation of inflammation and osteoclastogenesis related mRNA expressions while demonstrating a significant increase in the expression level of BMP2. Finally, we show that the bone defects healing effects as assessed using an aged rats' bone defects model. Ultimately, this work also provides insights into the design of effective biomaterials targeted at bone defects in the elderly.
创伤导致的骨缺损在老年人群中越来越常见。临床上,由于老年人的骨愈合能力相对降低,老年人的骨缺损修复仍然具有挑战性。开发针对老年人骨缺损的有效生物材料是骨组织工程策略的关键组成部分。然而,人们对老年人的骨再生关注甚少。在这里,我们开发了一种新型支架壳聚糖-硫酸软骨素锶(CH-SrCS),并评估了其改善骨再生的效果。我们发现 CH-SrCS 支架对下调炎症和破骨细胞生成相关 mRNA 表达有积极作用,同时 BMP2 的表达水平显著增加。最后,我们在老年大鼠骨缺损模型中评估了该支架的骨缺损愈合效果。最终,这项工作还为设计针对老年人骨缺损的有效生物材料提供了思路。