类风湿性关节炎
促炎细胞因子
关节炎
骨关节炎
医学
透皮
佐剂
炎症
药理学
免疫学
病理
替代医学
作者
Yixuan Lin,Yang Chen,Rong‐Hui Deng,Hao Qin,Nan Li,Yuting Qin,Hanqing Chen,Yaohua Wei,Zeming Wang,Qing Sun,Wenyi Qiu,Jian Shi,Long Chen,Yuguang Wang,Guangjun Nie,Ruifang Zhao
出处
期刊:Nano Today
[Elsevier]
日期:2023-02-25
卷期号:49: 101791-101791
被引量:24
标识
DOI:10.1016/j.nantod.2023.101791
摘要
Rheumatoid arthritis (RA) is a common chronic autoimmune disease and eventually ends in severe disability and death. RA has no cure, but there are some treatments for decreasing the severity of various symptoms. For example, pain management of RA by non-steroidal anti-inflammatory drugs (NSAIDs), neutralization of the inflammatory cytokines (or block their functions) of RA by specific biologics. However, the clinical benefit is limited due to their low permeability and poor bioavailability. Meanwhile, the system toxicity for long-term use of NSAIDs is another focal issue. Herein, degradable biopolymer microneedle patch was designed and synthesized. In this dual drug delivery patch, NSAIDs were encapsulated by polymeric nanoparticles, which were coated by the neutrophil membrane, followed by loaded into the microneedle patch for local transdermal delivery. When applied to the murine models, the microneedle patch gradually dissolves and releases the contained nanoparticles. Coating of neutrophil membrane provides the nanosized NSAIDs with the capability of cytokine binding and inflammatory joint tropism. Based on inflammatory microenvironment regulation by cytokine absorption and cyclooxygenase-2 inhibition, the microneedle shows a significant local anti-inflammatory therapeutic effect on mouse model of collagen-induced arthritis and rat model of adjuvant-induced arthritis. Further development based on this advanced strategy may provide additional therapeutic options for RA treatment.
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