A <sup>177</sup>Lu-nucleotide coordination polymer-incorporated thermosensitive hydrogel with anti-inflammatory and chondroprotective capabilities for osteoarthritis treatment.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39798244.
- Also identified by DOI 10.1016/j.biomaterials.2025.123098 and PMC identifier 11788045.
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Abstract
Osteoarthritis (OA) is a prevalent and debilitating condition characterized by cartilage destruction and inflammation. Traditional pharmacotherapies for OA are limited by their short-term efficacy and systemic side effects. Radiosynoviorthesis (RSO), involving intra-articular injection of radiopharmaceuticals, has shown promise for OA treatment but is hindered by the toxicity and rapid clearance of radioisotopes. Herein, we propose a novel strategy utilizing metal-organic coordination polymers (MCPs) as carrier of radioactive <sup>177</sup>Lu, with adenosine monophosphate (AMP) as ligand. We then incorporate the MCPs into chitosan/β-glycerophosphate thermosensitive hydrogels (<sup>177</sup>Lu/AMP@CG), which demonstrates enhanced retention of <sup>177</sup>Lu in the joint cavity. These hydrogels enable a single-dose intra-articular injection to provide sustained OA treatment without adverse effects. Combining <sup>177</sup>Lu-based RSO with the pharmacological properties of chitosan-based hydrogel yields exceptional anti-inflammatory, cartilage repair and protective effects. Together, this study underscores the significant local retention capacity of the <sup>177</sup>Lu/AMP@CG hydrogel and the potential of anti-inflammatory and chondroprotective strategy toward OA treatment.
Medical subject headings
- Osteoarthritis
- Anti-Inflammatory Agents
- Hydrogels
- Radioisotopes
- Lutetium
- Polymers