纳米药物靶向抗炎疗法,解决类风湿关节炎的 "症结"。

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY Journal of Drug Targeting Pub Date : 2024-04-01 Epub Date: 2024-02-16 DOI:10.1080/1061186X.2024.2315475
Min An, Juntao Zhang, Xiaojie Zhang, Yumeng Zhao, Yanhua Liu
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引用次数: 0

摘要

类风湿性关节炎是一种慢性、复杂的自身免疫性疾病,以炎症反应、滑膜增生、血管化、筋膜形成、软骨和骨破坏为特征,可导致关节畸形,甚至丧失功能,最终影响患者的健康和生活质量。虽然 RA 的发病机制尚不清楚,但越来越多的证据表明,炎症相关细胞浸润关节,造成组织损伤、炎症和疼痛。宿主耐受性和免疫平衡之间的平衡被打破,导致了 RA 的发展。现有的药物疗法和手术疗法无法彻底治愈 RA 或逆转其加速发展的趋势。因此,设计和开发合适有效的给药系统将大大提高治疗效果。本综述通过对类风湿性关节炎的炎症微环境及相关炎症细胞的描述,总结了该病的靶向策略及纳米技术的应用进展,有助于为类风湿性关节炎的后续治疗提供新思路。
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Nanomedicine targeted anti-inflammatory therapy to deal with the 'crux' of rheumatoid arthritis.

Rheumatoid arthritis is a chronic and complex autoimmune disease that is marked by an inflammatory response, synovial hyperplasia, vascularisation, fascial formation, cartilage and bone destruction, which can lead to joint deformity and even loss of function, ultimately affecting a person's health and quality of life. Although the pathogenesis of RA is unclear, growing evidence suggests that inflammation-associated cells infiltrate joints, causing tissue damage, inflammation and pain. This disruption in the balance between host tolerance and immune homeostasis the progression of RA. Existing drug therapy and surgical treatments for RA are unable to completely cure the disease or reverse its accelerated progression. Therefore, the design and development of an appropriate and effective drug delivery system will substantially improve the therapeutic effect. In this review, by describing the inflammatory microenvironment of rheumatoid arthritis and the associated inflammatory cells, the progress of targeting strategies and applications of nanotechnology in the disease is summarised, which will be helpful in providing new ideas for the subsequent treatment of rheumatoid arthritis.

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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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