4.8 Article

Mimicking Antioxidases and Hyaluronan Synthase: A Zwitterionic Nanozyme for Photothermal Therapy of Osteoarthritis

Journal

ADVANCED MATERIALS
Volume 35, Issue 44, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202303299

Keywords

dual-bionic nanozymes; hyaluronan synthase; lubrication replenishment; osteoarthritis; photothermal therapy

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A photothermal dual-bionic nanozyme, mimicking antioxidases and hyaluronan synthase, has been developed for effective osteoarthritis (OA) therapy. It can produce heat, scavenge free radicals, and promote chondrogenesis even under inflammatory conditions. This nanozyme regulates anabolic and catabolic processes simultaneously, thereby effectively restoring joint homeostasis and demonstrating an admirable photothermally therapeutic effect on OA.
Restoring joint homeostasis is crucial for relieving osteoarthritis (OA). Current strategies are limited to unilateral efforts in joint lubrication, inhibition of inflammation, free radicals scavenging, and cartilage regeneration. Herein, by modifying molybdenum disulfide (MoS2) with Mg2+-doped polydopamine and coating with polysulfobetaines, a dual-bionic photothermal nanozyme (MPMP) is constructed to mimic antioxidases/hyaluronan synthase for OA therapy. Photothermally enhanced lubrication lowers the coefficient of friction (0.028) in the early stage of OA treatment. The antioxidases-mimicking properties of MPMP nanozyme contribute to eliminating reactive oxygen and nitrogen species (ROS/RNS) (over 90% of scavenging ratio for H2O2/& BULL;OH/O & BULL;2-/DPPH/ABTS+) and supplying O2. With NIR irradiation, the MPMP nanozyme triggers thermogenesis (upregulating HSP70 expression) and Mg2+ release, which promotes the chondrogenesis in inflammatory conditions by deactivating NF-& kappa;B/IL-17 signaling pathways and enhancing MAPK signaling pathway. Benefiting from HSP70 and Mg2+, MPMP-NIR shows HAS-mimicking activity to increase the intracellular (twofold) and extracellular (3.12-fold) HA production. Therefore, MPMP-NIR demonstrates superior spatiotemporally therapeutic effect on OA in mice model, in terms of osteophytes (83.41% of reduction), OARSI scores (88.57% of reduction), and ACAN expression (2.70-fold of increment). Hence, insights into dual-bionic nanozymes can be a promising strategy for OA therapy or other inflammation-related diseases. A photothermal dual-bionic nanozyme (MPMP), mimicking antioxidases and hyaluronan synthase, is developed for effective osteoarthritis (OA) therapy, which can produce heat, scavenge free radical and promote chondrogenesis even if under inflammatory conditions. This nanozyme regulates anabolic and catabolic processes simultaneously, thereby restoring joint homeostasis effectively and demonstrating an admirable photothermally therapeutic effect on OA.image

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