ArticleBioactive materials2026
Mitochondria-targeted MXene-based nanozymes promote mitophagy and inhibit mtDNA-triggered cGAS/STING inflammation in osteoarthritis.
Article in Bioactive materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Osteoarthritis (OA) is a prevalent and debilitating joint disease driven by progressive cartilage degradation, mitochondrial dysfunction, and chronic inflammation. In this study, we introduced MS@PMXene-TK, an innovative, mitochondria-targeted nanozyme designed for cartilage repair by addressing these key pathological features. This nanozyme platform uniquely integrated a chondro-inductive peptide (SPPEPS)-loaded, polydopamine (PDA)-modified MXene core (S@PMXene) with a reactive oxygen species (ROS)-responsive thioketal-linked polyethylene glycol (PEG-TK) shell and a mitochondria-targeting peptide (MTP-131), enabling precise and responsive therapeutic intervention at the subcellular level.
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