首页> 外文期刊>Frontiers in Chemistry >Intra-articular Injection of Kartogenin-Incorporated Thermogel Enhancing Osteoarthritis Treatment
【24h】

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

机译:关节腔内注射与Kartogenin结合的热凝胶可增强骨关节炎的治疗

获取原文
       

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:为了提供用于软骨保护剂的持续释放的载体,以用于骨关节炎(OA)治疗的潜在应用,我们开发了结合了牛黄素(KGN)的热凝胶用于关节内注射。我们制造了聚乳酸(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。此外,与不添加热凝胶的软骨细胞相比,OA软骨细胞在KGN热凝胶中产生的2型胶原蛋白(COL-2)和糖胺聚糖(GAG)含量更高,基质金属蛋白酶13(MMP-13)含量更低。 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诱发的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治疗提供新的治疗方式。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号