Chen Weiying, Li Zuhao, Wang Zhenhong, Gao Hong, Ding Junyun, He Zhenzhou
School of Anesthesiology, Third Affiliated Hospital of Guizhou Medical University, Guiyang 550004, People's Republic of China.
Department of Anesthesiology, South Campus, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 201112, People's Republic of China.
J Pain Res. 2020 Dec 7;13:3315-3329. doi: 10.2147/JPR.S283518. eCollection 2020.
Pain and cartilage destruction caused by rheumatoid arthritis (RA) are major challenges during clinical treatment. Traditional systemic administration not only has obvious side effects but also provides limited relief for local symptoms in major joints. Local delivery of therapeutics for RA treatment is a potential strategy but is limited by rapid intraarticular release.
In this study, we prepared a thermoresponsive injectable hydrogel by mixing pluronic F127 (F127) and hyaluronic acid (HA) with poly (γ-glutamic acid) (PGA) incorporating infliximab (IFX), a new generation monoclonal antibody drug. We investigated the biocompatibility of the hydrogel and its IFX release profile. In vivo, we studied the clinical manifestations (articular skin temperature and joint diameter), detected cytokines in the synovial fluid and cartilage, performed behavioral studies on pain relief, and evaluated the cartilage protection effect.
A thermoresponsive hydrogel was successfully prepared by mixing F127, HA, and PGA with injectable properties. The F127-HA-PGA hydrogel had a porous structure with interconnected pores. The infliximab-loaded thermosensitive hydrogel exhibited good biocompatibility and biodegradability and sustained release properties. Intraarticular injection of the IFX-loaded F127-HA-PGA hydrogel could alleviate the expression of inflammatory cytokines, such as tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), interleukin-6 (IL-6), and interleukin-17 (IL-17), in the synovial fluid and cartilage as well as relieve pain and inhibit cartilage destruction in RA.
The double effect on pain relief and cartilage protection indicated the significant potential of the IFX-loaded injectable hydrogel for RA treatment in major joint lesions.
类风湿关节炎(RA)引起的疼痛和软骨破坏是临床治疗中的主要挑战。传统的全身给药不仅有明显的副作用,而且对主要关节的局部症状缓解有限。局部递送治疗药物用于RA治疗是一种潜在策略,但受到关节内快速释放的限制。
在本研究中,我们通过将普朗尼克F127(F127)、透明质酸(HA)与掺入英夫利昔单抗(IFX,一种新一代单克隆抗体药物)的聚(γ-谷氨酸)(PGA)混合,制备了一种热响应性可注射水凝胶。我们研究了水凝胶的生物相容性及其IFX释放曲线。在体内,我们研究了临床表现(关节皮肤温度和关节直径),检测了滑液和软骨中的细胞因子,进行了疼痛缓解的行为学研究,并评估了软骨保护作用。
通过将F127、HA和PGA混合成功制备了具有可注射特性的热响应性水凝胶。F127-HA-PGA水凝胶具有相互连通的孔隙的多孔结构。负载英夫利昔单抗的热敏水凝胶表现出良好的生物相容性、生物降解性和缓释特性。关节内注射负载IFX的F127-HA-PGA水凝胶可减轻滑液和软骨中炎性细胞因子如肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和白细胞介素-17(IL-17)的表达,以及缓解RA中的疼痛并抑制软骨破坏。
对疼痛缓解和软骨保护的双重作用表明负载IFX的可注射水凝胶在主要关节病变的RA治疗中具有显著潜力。