This paper demonstrated the hybridization of polyelectrolyte brushes with anti-inflammatory drug-loaded nanoMOFs that can achieve highly efficient aqueous lubrication and sustained drug release for the synergistic therapy of osteoarthritis (OA).… Click to show full abstract
This paper demonstrated the hybridization of polyelectrolyte brushes with anti-inflammatory drug-loaded nanoMOFs that can achieve highly efficient aqueous lubrication and sustained drug release for the synergistic therapy of osteoarthritis (OA). Poly(3-sulfopropyl methacrylate potassium salt) (PSPMK) brushes was grown on the surface of the UiO-66-NH2 via one-pot grafting polymerization, which served as a general surface modification method of NH2 -MOFs to grow the polymer brushes. The growth of the PSPMK brushes greatly enhance the stability, dispersity, and swelling of the nanoparticles in aqueous media. Using as lubricating additives, the UiO-66-NH2 @PSPMK achieved not only the reductions in both coefficient of friction and wear volume over 70% and 99% but also supported high load-carrying capacity and long-term durability. The PSPMK brushes could be used as a universal interfacial modification soft layer that can significantly improve the aqueous lubricating performance of other types of NH2 -MOFs. After encapsulating the anti-inflammatory aspirin (AS), the AS-UiO-66-NH2 @PSPMK showed both sustained drug release and good biocompatibility toward the human normal chondrocytes. Our work establishes anti-inflammatory drug-loaded UiO-66-NH2 @PSPMK as a potential multifunctional joint lubricant for OA treatment. This article is protected by copyright. All rights reserved.
               
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