Wang Fan, Han Xiaoyu, Han Zeyu, Wang Juan, Cai Zhengwei, Chen Gang, Bai Dingqun, Cui Wenguo
Department of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases, Shanghai Institute of Traumatology and Orthopaedics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin 2nd Road, Shanghai, 200025, P. R. China.
Jiaxing Key Laboratory of Basic Research and Clinical Translation on Orthopedic Biomaterials, Department of Orthopaedics, the Second Affiliated Hospital of Jiaxing University, Jiaxing, 314000, P. R. China.
Adv Mater. 2025 Feb;37(7):e2413156. doi: 10.1002/adma.202413156. Epub 2025 Jan 2.
High transductive loss at tissue injury sites impedes repair. The high dissipation characteristics in the electromechanical conversion of piezoelectric biomaterials pose a challenge. Therefore, supramolecular engineering and microfluidic technology is utilized to introduce slide-ring polyrotaxane and conductive polypyrrole to construct stress-electric coupling hydrogel microspheres. The molecular slippage mechanism of slide-ring structure stores and releases mechanical energy, reducing mechanical loss, the piezoelectric barium titanate enables stress-electricity conversion, and conjugated π-electron movement in conductive network improves the internal electron transfer efficiency of microspheres, thereby reducing the loss in stress-electricity conversion for the first time. Compared to traditional piezoelectric hydrogel microspheres, the stress-electric coupling efficiency of low-dissipation microspheres increased by 2.3 times, and the energy dissipation decreased to 43%. At cellular level, electrical signals generated by the microspheres triggered Ca influx into stem cells and upregulated the cAMP signaling pathways, promoting chondrogenic differentiation. Enhanced electrical signals induced macrophage polarization to the M2 phenotype, reshaping inflammation and promoting tissue repair. In vivo, the low-dissipation microspheres restored low-loss transduction between tissues, alleviated cartilage damage, improved behavioral outcomes, and promoted the treatment of osteoarthritis in rats. Therefore, this study proposes a new strategy for restoring low-loss transduction between tissues, particularly in mechanically sensitive tissues.
组织损伤部位的高传导损耗阻碍了修复。压电生物材料在机电转换过程中的高耗散特性带来了挑战。因此,利用超分子工程和微流控技术引入滑环聚轮烷和导电聚吡咯,构建应力 - 电耦合水凝胶微球。滑环结构的分子滑移机制储存和释放机械能,减少机械损耗,压电钛酸钡实现应力 - 电转换,导电网络中的共轭π电子运动提高了微球的内部电子转移效率,从而首次降低了应力 - 电转换中的损耗。与传统压电水凝胶微球相比,低耗散微球的应力 - 电耦合效率提高了2.3倍,能量耗散降至43%。在细胞水平上,微球产生的电信号触发钙离子流入干细胞并上调cAMP信号通路,促进软骨生成分化。增强的电信号诱导巨噬细胞极化为M2表型,重塑炎症并促进组织修复。在体内,低耗散微球恢复了组织间的低损耗传导,减轻了软骨损伤,改善了行为结果,并促进了大鼠骨关节炎的治疗。因此,本研究提出了一种恢复组织间低损耗传导的新策略,特别是在机械敏感组织中。