4.8 Article

Polymeric Aggregate-Embodied Hybrid Nitric-Oxide-Scavenging and Sequential Drug-Releasing Hydrogel for Combinatorial Treatment of Rheumatoid Arthritis

期刊

ADVANCED MATERIALS
卷 33, 期 34, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202008793

关键词

hydrogels; nitric oxide; rheumatoid arthritis; stimuli-responsive materials

资金

  1. National Research Foundation of Korea (NRF) [NRF-2017R1E1A1A01074088]
  2. Creative Materials Discovery Program through the NRF - Ministry of Science and ICT [NRF-2018M3D1A1058813]
  3. Korea Government (MSIT) [NRF-2020R1A4A1019456]
  4. OmniaMed Co., Ltd.
  5. National Research Foundation of Korea [4120200213576] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The study introduces a novel M-NO gel platform for the treatment of rheumatoid arthritis, which combines NO scavenging and sequential drug release to effectively alleviate symptoms in animal models, showing promising prospects for future use in combating inflammation and NO-related diseases.
Selective depletion of overproduced nitric oxide (NO) with nanoscavengers is a promising approach for treating rheumatoid arthritis (RA), preventing both oxidative/nitrosative stress and the upregulation of immune cells. However, its practical applications are limited owing to the minimum time interval between intra-articular injections and unwanted off-target NO depletion. Herein, the rational design of an injectable in situ polymeric aggregate-embodied hybrid NO-scavenging and sequential drug-releasing (M-NO) gel platform for the combinatorial treatment of RA by incorporating a clickable NO-cleavable cross-linker (DA-NOCCL) is reported. This network is held together with polymeric aggregates to achieve a self-healing capability for visco-supplementation and on-demand dual drug (both hydrophilic and hydrophobic)-releasing properties, depending on the NO concentration. Moreover, consecutive NO-scavenging action reduces pro-inflammatory cytokine levels in lipopolysaccharides-stimulated macrophage cell lines in vitro. Finally, the intra-articularly injected M-NO gel with anti-inflammatory dexamethasone significantly alleviates the symptoms of RA, with negligible toxicity, in animal models. It is believed that this novel M-NO gel platform will provide a guideline for the combinatorial treatment of RA and various NO-related diseases.

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