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Updated: Feb 15, 2026

An Adoptive Transfer Model of Rheumatoid Arthritis in Mice
Published on: June 6, 2025
Drug delivery targets and systems for targeted treatment of rheumatoid arthritis
1a Department of Sanitary Inspection, School of Public Health , Shenyang Medical College , Shenyang , China.
Abstract:
Rheumatoid arthritis (RA) is an immune-mediated inflammatory disease that selectively attacks human joints. The common non-targeted treatment approaches lead to obvious side effect and systemtic complication for RA patients. Therefore, targeted drug delivery for treatment of RA has gained much attetntion in the past few years. In this paper, we reviewed the potential targets (folate receptor, angiogenesis, matrix metalloproteases, selectins, vasoactive intestinal peptide receptor andFc-γ receptor) that could be utilised to facilitate the specific delivery of drugs to the inflammed synovium and also presented different drug delivery systems for targeting RA, including the liposomes, various types of nanoparticles, polymeric micelles and the macromolecular prodrugs. The strategies combining nanotechnologies and ligand mediated active targeting for RA would be emphatically illustrated, which was expected to be helpful for identifying technologies and drug delivery methods for targeted treatment of RA.
Insights
Targeted drug delivery shows promise for rheumatoid arthritis (RA) treatment, minimizing side effects. This review explores RA targets and nanotech-based delivery systems for enhanced joint inflammation therapy.
Area of Science:
- Immunology
- Pharmacology
- Biotechnology
Background:
- Rheumatoid arthritis (RA) is an immune-mediated inflammatory joint disease.
- Conventional treatments for RA often cause significant side effects and systemic complications.
- Targeted drug delivery strategies are emerging as a promising alternative for RA management.
Purpose of the Study:
- To review potential molecular targets within the inflamed synovium for RA treatment.
- To present various drug delivery systems designed for targeted RA therapy.
- To highlight the synergy of nanotechnology and active targeting for RA.
Main Methods:
- Literature review of RA-specific molecular targets.
- Analysis of drug delivery systems including liposomes, nanoparticles, micelles, and prodrugs.
- Examination of ligand-mediated active targeting strategies combined with nanomedicine.
Main Results:
- Identified key targets: folate receptor, angiogenesis, MMPs, selectins, VIPR, and Fc-γ receptor.
- Cataloged diverse nanocarriers and macromolecular prodrugs for targeted delivery.
- Demonstrated the potential of combining nanotechnology with active targeting for RA.
Conclusions:
- Targeted therapies offer a more specific approach to treating RA, reducing systemic toxicity.
- Nanotechnology-based delivery systems show significant potential for improving RA treatment efficacy.
- Further research into targeted drug delivery is crucial for advancing RA patient care.
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