Chen Yu-Ming, Wong Chin-Chean, Weng Pei-Wei, Chiang Chih-Wei, Lin Po-Yen, Lee Po-Wei, Jheng Pei-Ru, Hao Ping-Chien, Chen Yan-Ting, Cho Er-Chen, Chuang Er-Yuan
Graduate Institute of Biomedical Materials and Tissue Engineering, International Ph.D. Program in Biomedical Engineering, Graduate Institute of Nanomedicine and Medical Engineering, College of Biomedical Engineering, Taipei Medical University, Taipei 11031, Taiwan.
Department of Orthopedics, Shuang Ho Hospital, Taipei Medical University, New Taipei City 23561, Taiwan; Department of Orthopedics, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan; Research Center of Biomedical Devices, Taipei Medical University, Taipei 11031, Taiwan; International Ph.D. Program for Cell Therapy and Regenerative Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan.
Int J Biol Macromol. 2023 Oct 1;250:126105. doi: 10.1016/j.ijbiomac.2023.126105. Epub 2023 Aug 5.
Long-standing administration of disease-modifying antirheumatic drugs confirms their clinical value for managing rheumatoid arthritis (RA). Nevertheless, there are emergent worries over unwanted adverse risks of systemic drug administration. Hence, a novel strategy that can be used in a drug-free manner while diminishing side effects is immediately needed, but challenges persist in the therapy for RA. To this end, herein we conjugated tyramine (TYR) with alginate (ALG) to form ALG-TYR and then treated it for 5 min with oxygen plasma (ALG-TYR + P/5 min). It was shown that the ALG-TYR + P/5 min hydrogel exhibited favorable viscoelastic, morphological, mechanical, biocompatible, and cellular heat-shock protein amplification behaviors. A thorough physical and structural analysis was conducted on the ALG-TYR + P/5 min hydrogel, revealing favorable physical characteristics and uniform porous structural features within the hydrogel. Moreover, ALG-TYR + P/5 min not only effectively inhibited inflammation of RA but also potentially regulated lesion immunity. Once ALG-TYR + P/5 min was intra-articularly administered to joints of rats with zymosan-induced arthritis, we observed that ALG-TYR + P/5 min could ameliorate syndromes of RA joint. This bioinspired and self-restorable ALG-TYR + P/5 min hydrogel can thus serve as a promising system to provide prospective outcomes to potentiate RA therapy.
长期使用改善病情抗风湿药物证实了它们在治疗类风湿性关节炎(RA)方面的临床价值。然而,人们开始担心全身给药带来的不良风险。因此,迫切需要一种能够以无药物方式使用同时减少副作用的新策略,但RA治疗仍面临挑战。为此,我们在此将酪胺(TYR)与藻酸盐(ALG)共轭形成ALG-TYR,然后用氧等离子体处理5分钟(ALG-TYR + P/5分钟)。结果表明,ALG-TYR + P/5分钟水凝胶表现出良好的粘弹性、形态、力学、生物相容性和细胞热休克蛋白扩增行为。对ALG-TYR + P/5分钟水凝胶进行了全面的物理和结构分析,揭示了其良好的物理特性和水凝胶内均匀的多孔结构特征。此外,ALG-TYR + P/5分钟不仅有效抑制了RA的炎症,还潜在地调节了损伤免疫。一旦将ALG-TYR + P/5分钟关节内注射到酵母聚糖诱导的关节炎大鼠的关节中,我们观察到ALG-TYR + P/5分钟可以改善RA关节的症状。因此,这种受生物启发且可自我修复的ALG-TYR + P/5分钟水凝胶可以作为一个有前景的系统,为增强RA治疗提供预期结果。