Skip to content
Review Open access

Nanomedicine Approaches for Rheumatoid Arthritis (RA): Targeted Therapy and Controlled Drug Release

Sep 2026 · Journal of Drug Delivery and Therapeutics · 0 citations · 72 references

TL;DR

Advanced nanomedicine represents a promising strategy for improving the safety, efficacy, and personalization of rheumatoid arthritis treatment and holds significant potential for transforming future clinical management of this debilitating autoimmune disease.

Abstract

Rheumatoid arthritis (RA) is a chronic, systemic autoimmune disorder characterized by persistent synovial inflammation, progressive cartilage degradation, bone erosion, and joint deformity, ultimately leading to functional disability and reduced quality of life. Despite significant advances in disease management, conventional therapeutic approaches, including nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, conventional disease-modifying antirheumatic drugs (DMARDs), biologic agents, and Janus kinase (JAK) inhibitors, are frequently associated with limited tissue specificity, poor pharmacokinetic profiles, systemic adverse effects, and variable patient responses. These limitations have driven the development of nanomedicine-based drug delivery systems that offer enhanced targeting capabilities, improved drug stability, prolonged circulation time, and controlled drug release at inflamed joints. This review comprehensively summarizes recent advances in nanomedicine approaches for rheumatoid arthritis, with particular emphasis on targeted therapy and controlled drug release strategies. The review discusses the design principles and therapeutic potential of various nanocarriers, including liposomes, polymeric nanoparticles, dendrimers, solid lipid nanoparticles, nanostructured lipid carriers, polymeric micelles, metallic nanoparticles, mesoporous silica nanoparticles, hydrogels, and extracellular vesicle-based systems. It further explores passive and active targeting mechanisms, stimuli-responsive drug release platforms, and nanocarrier-mediated delivery of anti-inflammatory agents, biologics, nucleic acids, and emerging therapeutics. Recent preclinical and clinical developments demonstrating improved therapeutic efficacy, reduced systemic toxicity, enhanced bioavailability, and modulation of inflammatory pathways are critically evaluated. Furthermore, the review highlights current challenges related to biological barriers, long-term biosafety, large-scale manufacturing, regulatory approval, and clinical translation while discussing emerging trends such as biomimetic nanocarriers, artificial intelligence-assisted nanomedicine design, precision medicine, and multifunctional theranostic platforms. Overall, advanced nanomedicine represents a promising strategy for improving the safety, efficacy, and personalization of rheumatoid arthritis treatment and holds significant potential for transforming future clinical management of this debilitating autoimmune disease. Keywords: Rheumatoid arthritis; Nanomedicine; Targeted drug delivery; Controlled drug release; Nanocarriers.

Read PDF

Similar papers

Review Open access Sep 2026

Polysaccharide-Derived Drug Delivery Systems: Therapeutic Potential in Rheumatoid Arthritis—A Review

Rheumatoid arthritis (RA) is a systemic autoimmune disease characterized by chronic synovial inflammation, synovial hyperplasia, and progressive joint destruction and remains a major clinical challenge. Polysaccharide-derived delivery platforms have attracted widespread attention for RA precision therapy owing to their...

Xiao-Tong Yue, Ai-Shuo Yu, Jin-Jin Chen et al. · 0 citations
Sep 2026

Nanostructured Cubosomal Gels for Targeted Drug Delivery in Rheumatoid Arthritis: Advances in Nanomedicine and Therapeutic Nanotechnology.

Introduction/ Objective: Rheumatoid Arthritis (RA) is an autoimmune disease characterized by chronic inflammation of the synovial joints, leading to joint destruction and systemic complications. Existing therapies, such as Disease-Modifying Antirheumatic Drugs (DMARDs) and Nonsteroidal Anti-Inflammatory Drugs (NSAIDs),...

Ashok Thulluru, C. Jangme, Vrushabh Patil · 0 citations
#gene editing Review Sep 2026

Nanocarrier-enabled Gene and Nucleic Acid Therapeutics for Rheumatoid Arthritis: Advances, Translational Evidence, and Regulatory Challenges.

The available evidence underscores both the therapeutic potential and inherent complexity of nanocarrier-mediated gene and nucleic acid therapies for RA, emphasizing the necessity for optimized delivery strategies, rigorous safety assessments, and biomarker-guided patient stratification to achieve successful clinical t...

SaiGeetha Meka, Sarfaroz Shaik A, Vandana Dasari et al. · 0 citations
Review Open access Sep 2026

Natural Polysaccharides for Rheumatoid Arthritis Therapy: Mechanism, Drug Delivery and Clinical Application.

This review systematically summarizes the pharmacodynamic basis and molecular mechanisms underlying the anti-RA effects of natural polysaccharides reported since 2000, with particular emphasis on recent advances in novel drug delivery technologies and a critical evaluation of clinical application studies.

Lu-Xin Li, Jun-Nan Li, Guang-Zhi Li et al. · 0 citations
Review Open access Sep 2026

A Review on Rheumatoid Arthritis and Its Newer Treatment (PRP)

: Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disorder characterized by persistent synovial inflammation, progressive cartilage and joint damage, pain, stiffness, and functional disability. Although conventional therapies, including disease-modifying antirheumatic drugs (DMARDs), biologic agents, cor...

Kamali I, L. K · 0 citations
Review Sep 2026

Opening Avenues for Rheumatoid Arthritis Treatment via Transdermal Application of Microneedles: Progress so far and Future Outlook

Rheumatoid arthritis (RA) is a chronic autoimmune disease with a global prevalence of 0.5% to 2%, causing serious impairment and early mortality. Presently approved therapeutics comprising non‐steroidal anti‐inflammatory drugs (NSAIDs), disease‐modifying anti‐rheumatic drugs (DMARDs), corticosteroids, etc. only lower p...

K. Kolekar, Bushra Bashir, P. Kumbhar et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.