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Intra-articular Injection of Kartogenin-Incorporated Thermogel Enhancing Osteoarthritis Treatment

机译:关节腔内注射结合有Kartogenin的热凝胶可增强骨关节炎的治疗

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摘要

To provide a vehicle for sustained release of cartilage-protective agent for the potential application of osteoarthritis (OA) treatment, we developed a kartogenin (KGN)-incorporated thermogel for intra-articular injection. We fabricated a poly(lactide-co-glycolide)-block-poly(ethylene glycol)-block-poly(lactide-co-glycolide) (PLGA–PEG–PLGA) thermogel as a KGN carrier for IA injection. OA chondrocytes were cultured in thermogel with or with no KGN to investigate the effect of KGN thermogel on cartilage matrix. The in vivo effect of KGN thermogel on OA was examined in a rabbit OA model. The KGN thermogel showed a sustained in vitro release of KGN for 3 weeks. OA chondrocytes proliferated well both in thermogel and KGN thermogel. In addition, OA chondrocytes produced higher amount of [type 2 collagen (COL-2) and glycosaminoglycan (GAG)], as well as lower level of matrix metalloproteinase 13 (MMP-13) in KGN thermogel that those in thermogel with no addition of KGN. The gene analysis supported that KGN thermogel enhanced expression of hyaline-cartilage specific genes Col 2 and AGC, and inhibited the expression of MMP-13. Compared with intra-articular injection of saline or thermogel containing no KGN, KGN thermogel can enhance cartilage regeneration and inhibit joint inflammation of arthritic knees in a rabbit ACLT-induced OA model at 3 weeks after the injection. Therefore, the KGN-incorporated PLGA–PEG–PLGA thermogel may provide a novel treatment modality for OA treatment with IA injection.
机译:为了为软骨保护剂的潜在应用提供一种持续释放软骨保护剂的载体,我们开发了结合了牛黄素(KGN)的热凝胶用于关节内注射。我们制造了聚(丙交酯-共-乙交酯)-嵌段-聚(乙二醇)-嵌段-聚(丙交酯-共-乙交酯)(PLGA-PEG-PLGA)热凝胶,作为用于IA注射的KGN载体。在有或没有KGN的热凝胶中培养OA软骨细胞,以研究KGN热凝胶对软骨基质的影响。在兔OA模型中检查了KGN热凝胶对OA的体内作用。 KGN热凝胶显示KGN在体外持续释放3周。 OA软骨细胞在热凝胶和KGN热凝胶中均增殖良好。另外,OA软骨细胞在KGN热凝胶中产生的[2型胶原(COL-2)和糖胺聚糖(GAG)]量更高,而基质金属蛋白酶13(MMP-13)的水平比在不加入热凝胶的情况下更低。 KGN。基因分析支持KGN热凝胶增强了透明质酸特异基因Col 2和AGC的表达,并抑制了MMP-13的表达。与关节腔内注射不含KGN的盐水或热凝胶相比,在注射后3周,KGN热凝胶可增强兔ACLT诱导的OA模型的软骨再生并抑制关节炎的膝关节发炎。因此,结合KGN的PLGA–PEG–PLGA热凝胶可能为IA注射进行OA治疗提供一种新颖的治疗方式。

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