Li Jianan, Li Lang, Wu Tingkui, Shi Kun, Bei Zhongwu, Wang Meng, Chu Bingyang, Xu Keqi, Pan Meng, Li Yicong, Hu Xulin, Zhang Linghong, Qu Ying, Qian Zhiyong
Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China.
Department of Pediatric Surgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Small Methods. 2024 Jan;8(1):e2300843. doi: 10.1002/smtd.202300843. Epub 2023 Oct 6.
Bone defects in osteoporosis usually present excessive reactive oxygen species (ROS), abnormal inflammation levels, irregular shapes and impaired bone regeneration ability; therefore, osteoporotic bone defects are difficult to repair. In this study, an injectable thermosensitive hydrogel poly (D, L-lactide)-poly (ethylene glycol)- poly (D, L-lactide) (PLEL) system containing resveratrol (Res) and dexamethasone (DEX) is designed to create a microenvironment conducive to osteogenesis in osteoporotic bone defects. This PLEL hydrogel is injected and filled irregular defect areas and achieving a rapid sol-gel transition in situ. Res has a strong anti-inflammatory effects that can effectively remove excess free radicals at the damaged site, guide macrophage polarization to the M2 phenotype, and regulate immune responses. Additionally, DEX can promote osteogenic differentiation. In vitro experiments showed that the hydrogel effectively promoted osteogenic differentiation of mesenchymal stem cells, removed excess intracellular ROS, and regulated macrophage polarization to reduce inflammatory responses. In vivo experiments showed that the hydrogel promoted osteoporotic bone defect regeneration and modulated immune responses. Overall, this study confirmed that the hydrogel can treat osteoporotic bone defects by synergistically modulating bone damage microenvironment, alleviating inflammatory responses, and promoting osteogenesis; thus, it represents a promising drug delivery strategy to repair osteoporotic bone defects.
骨质疏松症中的骨缺损通常表现为活性氧(ROS)过量、炎症水平异常、形状不规则以及骨再生能力受损;因此,骨质疏松性骨缺损难以修复。在本研究中,设计了一种含有白藜芦醇(Res)和地塞米松(DEX)的可注射热敏水凝胶聚(D,L-丙交酯)-聚(乙二醇)-聚(D,L-丙交酯)(PLEL)系统,以在骨质疏松性骨缺损中营造有利于成骨的微环境。这种PLEL水凝胶被注射并填充到不规则的缺损区域,并在原位实现快速的溶胶-凝胶转变。Res具有强大的抗炎作用,可有效清除受损部位的过量自由基,引导巨噬细胞极化为M2表型,并调节免疫反应。此外,DEX可促进成骨分化。体外实验表明,该水凝胶有效促进间充质干细胞的成骨分化,清除细胞内过量的ROS,并调节巨噬细胞极化以减轻炎症反应。体内实验表明,该水凝胶促进骨质疏松性骨缺损的再生并调节免疫反应。总体而言,本研究证实该水凝胶可通过协同调节骨损伤微环境、减轻炎症反应和促进成骨来治疗骨质疏松性骨缺损;因此,它代表了一种修复骨质疏松性骨缺损的有前景的药物递送策略。