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仿生型 NO 清除透明质酸纳米粒子实现 MTX 的靶向递送和类风湿关节炎的综合管理。

Biomimetic NO Scavenging Hyaluronic Acid Nanoparticles Enable Targeted Delivery of MTX and Integrated Management of Rheumatoid Arthritis.

机构信息

Electrocardiogram Room, First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, P.R. China.

Xingguo County Maternal and Child Health Hospital, Xingguo 342400, P.R. China.

出版信息

Biomacromolecules. 2024 Jul 8;25(7):4557-4568. doi: 10.1021/acs.biomac.4c00556. Epub 2024 Jun 20.

Abstract

Rheumatoid arthritis (RA) is a complicated chronic disorder of the immune system, featured with severe inflammatory joints, synovium hyperplasia, articular cartilage, and bone damage. In the RA microenvironment, RA-involved cells, overproduced nitric oxide (NO), and pro-inflammatory cytokines are highly interplayed and mutually reinforced, which form a vicious circle and play crucial roles in the formation and progression of RA. To comprehensively break the vicious circle and obtain the maximum benefits, we have developed neutrophil membrane-camouflaged NO scavenging nanoparticles based on an NO-responsive hyaluronic acid derivative for delivery of MTX. These multifunctional nanoparticles (NNO-NPs/MTX), by inheriting the membrane functions of the source cells, possess prolonged circulation and specific localization at the inflamed sites when administrated in the body. Remarkably, NNO-NPs/MTX can neutralize the pro-inflammatory cytokines via the outer membrane receptors, scavenge NO, and be responsively disassociated to release MTX for RA-involved cell regulation and HA for lubrication in the RA sites. In a collagen-induced arthritis mouse model, NNO-NPs/MTX exhibits a significant anti-inflammation effect and effectively alleviates the characteristic RA symptoms such as synovial hyperplasia and cartilage destruction, realizing the synergistic and boosted therapeutic outcome against intractable RA. Thus, NNO-NPs/MTX provides a promising and potent platform to integrately treat RA.

摘要

类风湿性关节炎(RA)是一种复杂的慢性免疫系统紊乱疾病,其特征为严重的炎症关节、滑膜增生、关节软骨和骨损伤。在 RA 微环境中,RA 相关细胞、过度产生的一氧化氮(NO)和促炎细胞因子高度相互作用和相互加强,形成恶性循环,在 RA 的形成和进展中发挥关键作用。为了全面打破恶性循环并获得最大效益,我们开发了基于 NO 响应透明质酸衍生物的中性粒细胞膜伪装的 NO 清除纳米粒子,用于输送 MTX。这些多功能纳米粒子(NNO-NPs/MTX)通过继承源细胞的膜功能,在体内给药时具有延长的循环时间和在炎症部位的特异性定位。值得注意的是,NNO-NPs/MTX 可以通过外膜受体中和促炎细胞因子,清除 NO,并响应性解离以释放 MTX 用于调节 RA 相关细胞,以及用于 RA 部位的润滑。在胶原诱导的关节炎小鼠模型中,NNO-NPs/MTX 表现出显著的抗炎作用,并有效缓解 RA 的特征性症状,如滑膜增生和软骨破坏,实现了针对难治性 RA 的协同和增强治疗效果。因此,NNO-NPs/MTX 为综合治疗 RA 提供了一个有前途和有效的平台。

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