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载抗炎肽的关节内注射聚糖/褐藻聚糖纳米凝胶抑制炎症和减轻骨关节炎进展。

Intra-articular injection of anti-inflammatory peptide-loaded glycol chitosan/fucoidan nanogels to inhibit inflammation and attenuate osteoarthritis progression.

机构信息

Center for Joint Surgery, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing 400038, China; Institute of Combined Injury, State Key Laboratory of Trauma, Burns and Combined Injury, Chongqing Engineering Research Center for Nanomedicine, Department of Preventive Medicine, Third Military Medical University (Army Medical University), Chongqing 400038, China.

Center for Joint Surgery, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing 400038, China.

出版信息

Int J Biol Macromol. 2021 Feb 15;170:469-478. doi: 10.1016/j.ijbiomac.2020.12.158. Epub 2020 Dec 24.

DOI:10.1016/j.ijbiomac.2020.12.158
PMID:33359610
Abstract

Glycol chitosan/fucoidan nanogels loaded with anti-inflammatory peptide KAFAK (GC/Fu@KAFAK NGs) were fabricated based on the electrostatic interaction and genipin cross-linking methods. The prepared NGs had an average size of 286.3 ± 5.0 nm and positive surface charge of 14.0 ± 0.2 mV. The anti-inflammatory and chondro-protective effects of GC/Fu@KAFAK NGs were evaluated on interlecukin-1β (IL-1β)-stimulated rat chondrocytes. We found that GC/Fu@KAFAK NGs not only inhibited the expression of inflammatory factors interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-α), but also enhanced the expression of chondrogenic markers type II collagen, aggrecan, and Sox9. More importantly, in rat osteoarthritis (OA) model, the intra-articular (IA) injection of GC/Fu@KAFAK NGs reduced glycosaminoglycan loss and diminished inflammatory cytokine release. In addition, GC/Fu@KAFAK NGs showed good biocompatibility both in vitro and in vivo. In conclusion, IA inject-able GC/Fu@KAFAK NGs might have great potential in OA treatment.

摘要

基于静电相互作用和京尼平交联方法,制备了载有抗炎肽 KAFAK 的乙二醇壳聚糖/褐藻糖胶纳米凝胶(GC/Fu@KAFAK NGs)。所制备的 NGs 的平均粒径为 286.3±5.0nm,表面带正电荷 14.0±0.2mV。在白细胞介素-1β(IL-1β)刺激的大鼠软骨细胞上评价了 GC/Fu@KAFAK NGs 的抗炎和软骨保护作用。结果发现,GC/Fu@KAFAK NGs 不仅抑制了炎症因子白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的表达,而且增强了软骨形成标志物 II 型胶原、聚集蛋白聚糖和 Sox9 的表达。更重要的是,在大鼠骨关节炎(OA)模型中,关节内(IA)注射 GC/Fu@KAFAK NGs 减少了糖胺聚糖的丢失和炎症细胞因子的释放。此外,GC/Fu@KAFAK NGs 在体内外均表现出良好的生物相容性。总之,IA 可注射的 GC/Fu@KAFAK NGs 在 OA 治疗中可能具有巨大的潜力。

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