Xing Zhe, Liang Jingwen, Sun Yang, Dai Jing, Cai Jiazheng, Fujio Masahito, Xu Yiwen, An Xiaoli, Xue Ying
School/Hospital of Stomatology, Lanzhou University, Lanzhou 730000, China.
Key Laboratory of Dental Maxillofacial Reconstruction and Biological Intelligence Manufacturing, Lanzhou University, Lanzhou 730000, China.
Pharmaceutics. 2025 May 13;17(5):643. doi: 10.3390/pharmaceutics17050643.
Constant inflammation can be a detrimental response in bone regeneration. To regulate of the inflammatory response and synchronically promote rapid tissue regeneration is a vital clinical challenge. The urinary bladder matrix (UBM) and small intestinal submucosa (SIS) composite are commonly used extracellular matrix (ECM) materials. We designed a novel drug-loaded membrane by integrating the biological matrix (BM) composed of UBM and SIS composites with Resolvin D1 (RvD1), an endogenous pro-resolving lipid mediator, using the lyophilization process. This membrane is referred to as BRL, an acronym for BM-RvD1-Lyophilization. : In this study, the physicochemical properties of the membranes were characterized. Fluorescence staining and the CCK8 assay kit were utilized to assess biocompatibility. To evaluate the inflammatory resolution properties and osteogenic ability of osteoblasts, real-time quantitative PCR and ELISA were conducted. : BRL exhibited a more pronounced three-dimensional pore structure, demonstrating excellent physicochemical properties and enabling the slow release of RvD1. This approach improved the viability of MG63 osteoblast-like cells, reduced LPS-induced inflammation, and upregulated osteogenesis-related genes significantly. : By integrating inflammation control capabilities into tissue regeneration materials, BRL effectively regulates the tissue regeneration microenvironment, thereby enhancing regeneration efficiency and positioning itself as an exceptional candidate for future tissue regeneration membranes.
持续的炎症反应在骨再生过程中可能是一种有害的反应。调节炎症反应并同时促进组织快速再生是一项至关重要的临床挑战。膀胱基质(UBM)和小肠黏膜下层(SIS)复合材料是常用的细胞外基质(ECM)材料。我们通过冻干工艺,将由UBM和SIS复合材料组成的生物基质(BM)与内源性促消退脂质介质Resolvin D1(RvD1)整合,设计出一种新型载药膜。这种膜被称为BRL,是BM - RvD1 - 冻干法的首字母缩写。在本研究中,对该膜的物理化学性质进行了表征。利用荧光染色和CCK8检测试剂盒评估生物相容性。为了评估成骨细胞的炎症消退特性和成骨能力,进行了实时定量PCR和ELISA检测。BRL呈现出更明显的三维孔结构,具有优异的物理化学性质,并能使RvD1缓慢释放。这种方法提高了MG63成骨样细胞的活力,减轻了脂多糖诱导的炎症反应,并显著上调了成骨相关基因。通过将炎症控制能力整合到组织再生材料中,BRL有效地调节了组织再生微环境,从而提高了再生效率,使其成为未来组织再生膜的优秀候选材料。