# Smart Hydrogel for the Treatment of Rheumatoid Arthritis

**Authors:** Wenfeng Jiao, Xueya Wang, Hui Xu, Yang Fei, Yong Jin

PMC · DOI: 10.3390/gels12030209 · 2026-03-04

## TL;DR

This paper reviews smart hydrogels as a potential advanced treatment for rheumatoid arthritis, focusing on their design and challenges in clinical translation.

## Contribution

The paper provides a systematic review of preparation strategies and stimulus-responsive mechanisms of smart hydrogels for rheumatoid arthritis treatment.

## Key findings

- Smart hydrogels offer targeted and controlled drug delivery in the inflamed joint microenvironment.
- Temperature-responsive and multi-responsive hydrogels are most frequently studied for localized therapy.
- Clinical translation is hindered by biocompatibility, standardization, and manufacturing challenges.

## Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune disease that imposes substantial physical, emotional, and socioeconomic burdens on patients. Conventional therapeutic approaches are often limited by systemic toxicity, inadequate joint targeting, and variable patient responses, highlighting the urgent need for advanced drug delivery systems. Smart hydrogels have emerged as a promising platform for RA treatment due to their unique three-dimensional hydrophilic networks, excellent biocompatibility, and tunable physicochemical properties. This review systematically summarizes the preparation strategies and design principles of smart hydrogels, with an emphasis on chemically and physically crosslinked networks as well as composite systems. It further outlines the major stimulus-responsive release mechanisms—including temperature, pH, reactive oxygen species (ROS), light, and enzyme triggers—that enable targeted and controlled drug delivery within the inflamed joint microenvironment. Among the various types discussed, temperature-responsive and multi-responsive hydrogels are most frequently investigated for their potential to achieve localized, on-demand therapy. Despite considerable preclinical progress, the clinical translation of smart hydrogels faces critical challenges, including insufficient long-term biocompatibility data, lack of standardized evaluation protocols, and difficulties in scalable manufacturing. This review aims to provide a conceptual framework for the rational design of smart hydrogels and to stimulate interdisciplinary efforts toward overcoming existing translational barriers in RA treatment.

## Linked entities

- **Diseases:** Rheumatoid arthritis (MONDO:0008383)

## Full-text entities

- **Genes:** Nr4a1 (nuclear receptor subfamily 4, group A, member 1) [NCBI Gene 79240] {aka HMR, Ngfi-b, Nur77}, CCL20 (C-C motif chemokine ligand 20) [NCBI Gene 6364] {aka CKb4, Exodus, LARC, MIP-3-alpha, MIP-3a, MIP3A}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}, RELA (RELA proto-oncogene, NF-kB subunit) [NCBI Gene 5970] {aka AIF3BL3, CMCU, NFKB3, p65}, CHUK (component of inhibitor of nuclear factor kappa B kinase complex) [NCBI Gene 1147] {aka BPS2, IKBKA, IKK-1, IKK-alpha, IKK1, IKKA}, NFKBIA (NFKB inhibitor alpha) [NCBI Gene 4792] {aka EDAID2, IKBA, MAD-3, NFKBI}, SYK (spleen associated tyrosine kinase) [NCBI Gene 6850] {aka IMD82, p72-Syk}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, RENBP (renin binding protein) [NCBI Gene 5973] {aka RBP, RNBP}, IKBKB (inhibitor of nuclear factor kappa B kinase subunit beta) [NCBI Gene 3551] {aka IKK-2, IKK-beta, IKK2, IKKB, IMD15, IMD15A}, AGER (advanced glycosylation end-product specific receptor) [NCBI Gene 177] {aka RAGE, SCARJ1, sRAGE}, BMP1 (bone morphogenetic protein 1) [NCBI Gene 649] {aka OI13, PCOLC, PCP, TLD}, CS (citrate synthase) [NCBI Gene 1431], MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313] {aka CLG4, CLG4A, MMP-2, MMP-II, MONA, TBE-1}, IL17RA (interleukin 17 receptor A) [NCBI Gene 23765] {aka CANDF5, CD217, CDw217, IL-17RA, IL17R, IMD51}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, Tet2 (tet methylcytosine dioxygenase 2) [NCBI Gene 310859] {aka RGD1311625}, CGAS (cyclic GMP-AMP synthase) [NCBI Gene 115004] {aka C6orf150, D4, MB21D1, h-cGAS}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, HSP90B2P (heat shock protein 90 beta family member 2, pseudogene) [NCBI Gene 7190] {aka GRP94P1, GRP94b, HSP, HSPCP2, TRA1P1, TRAP1}, EGF (epidermal growth factor) [NCBI Gene 1950] {aka HOMG4, URG}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960] {aka CDW44, CSPG8, ECM-III, ECMR-III, H-CAM, HCELL}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CP (ceruloplasmin) [NCBI Gene 1356] {aka AB073614, CP-2}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}
- **Diseases:** type 1 diabetes (MESH:D003922), pain (MESH:D010146), events (MESH:D002318), cytotoxic (MESH:D064420), arthritis (MESH:D001168), gastrointestinal irritation (MESH:D005767), RA (MESH:D001172), osteolysis (MESH:D010014), ILD (MESH:D017563), inflammatory bowel disease (MESH:D015212), infections (MESH:D007239), injury to (MESH:D014947), systemic autoimmune disorder (MESH:D020274), immune dysregulation (OMIM:614878), swelling (MESH:D004487), synovial hyperplasia (MESH:D006965), Synovitis (MESH:D013585), autoimmune inflammatory disorder (MESH:D007249), pulmonary fungal infections (MESH:D008172), bone erosion (MESH:D014077), deformity (MESH:D009140), erythema (MESH:D004890), bone and cartilage damage (MESH:D002357), autoimmune disease (MESH:D001327), Joint Destruction (MESH:D008105), joint damage (MESH:D007592), cancer (MESH:D009369), multiple sclerosis (MESH:D009103)
- **Chemicals:** ZnO (MESH:D015034), CS (MESH:D048271), azobenzene (MESH:C009850), PEG-dithiol (MESH:C535242), thioether (MESH:D013440), PGI2 (MESH:D011464), benzotriazole (MESH:C012771), Tetrandrine (MESH:C009438), Dexamethasone (MESH:D003907), C3H8O3 (MESH:D005990), CaCl2 (MESH:D002122), glucosamine (MESH:D005944), HA (MESH:D006820), Schiff base (MESH:D012545), DOX (MESH:D004317), gold (MESH:D006046), starch (MESH:D013213), polysaccharide (MESH:D011134), lipid (MESH:D008055), beta-lactam (MESH:D047090), Nap peptide (MESH:C425904), hydrazone (MESH:D006835), glycyrrhizic acid (MESH:D019695), infliximab (MESH:D000069285), MXene (MESH:C000723374), poly (N-isopropylacrylamide (MESH:C052970), calcium (MESH:D002118), curcumin (MESH:D003474), Hydrogen (MESH:D006859), NO (MESH:D009569), polymer (MESH:D011108), gallic acid (MESH:D005707), tocilizumab (MESH:C502936), BiMP (-), beta-GP (MESH:C031463), oxygen (MESH:D010100), PVA (MESH:D011142), o-phenylenediamine (MESH:C034193), rapamycin (MESH:D020123), carbon (MESH:D002244), mercury (MESH:D008628), MoO2 (MESH:C539565), polylactic acid (MESH:C033616), disulfide (MESH:D004220), superoxide (MESH:D013481), thiol (MESH:D013438), chondroitin sulfate (MESH:D002809), PGD2 (MESH:D015230), Sodium alginate (MESH:D000464), ALG (MESH:D000077322), S-G (MESH:C000603632), NH3 (MESH:D000641), camptothecin (MESH:D002166), Metal (MESH:D008670), 3,4-dihydroxyphenylacetic acid (MESH:D015102), dextran sulfate (MESH:D016264), MoS2 (MESH:C082964), water (MESH:D014867), black phosphorus (MESH:D010758), polyacrylamide (MESH:C016679)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13025333/full.md

---
Source: https://tomesphere.com/paper/PMC13025333