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Photo-crosslinked HAMA hydrogel with cordycepin encapsulated chitosan microspheres for osteoarthritis treatment

机译:光交联的HAMA水凝胶与虫草素封装的壳聚糖微球用于骨关节炎的治疗

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摘要

Autophagy is a protective mechanism in normal cartilage. The present study aimed to investigate the synergistic therapeutic effect of promotion of chondrocyte autophagy via exposure to cordycepin encapsulated by chitosan microspheres (CM-cordycepin) and photo-crosslinked hyaluronic acid methacrylate (HAMA) hydrogel, with the goal of evaluating CM-cordycepin as a treatment for patients with osteoarthritis. First, we developed and evaluated the characteristics of HAMA hydrogels and chitosan microspheres. Next, we measured the effect of cordycepin on cartilage matrix degradation induced by IL1-β in chondrocytes and an ex vivo model. Cordycepin protects cartilage from degradation partly by activation of autophagy. Moreover, we surgically induced osteoarthritis in mice, which were injected intra-articularly with CM-cordycepin and HAMA. The combination of CM-cordycepin and HAMA hydrogel retarded the progression of surgically induced OA. Cordycepin ameliorated cartilage matrix degradation at least partially by inducing autophagy in vivo. Our results demonstrate that the combination of cordycepin encapsulated by CMs and photo-crosslinked HAMA hydrogel could be a promising strategy for treating patients with osteoarthritis.
机译:自噬是正常软骨的一种保护机制。本研究旨在探讨通过暴露于壳聚糖微球(CM-cordycepin)封装的虫草素和光交联的透明质酸甲基丙烯酸透明质酸(HAMA)水凝胶促进软骨细胞自噬的协同治疗作用,以评估CM-cordycepin为骨关节炎患者的治疗。首先,我们开发并评估了HAMA水凝胶和壳聚糖微球的特性。接下来,我们测量了虫草素对软骨细胞和离体模型中IL1-β诱导的软骨基质降解的影响。虫草素部分地通过激活自噬来保护软骨免于降解。此外,我们通过外科手术在小鼠中诱发了骨关节炎,并在关节内注射CM-cordycepin和HAMA。 CM-cordycepin和HAMA水凝胶的组合可延缓手术诱发的OA的进展。虫草素通过在体内诱导自噬至少部分地改善了软骨基质的降解。我们的结果表明,由CMs封装的虫草素和光交联的HAMA水凝胶的组合可能是治疗骨关节炎患者的有前途的策略。

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