Ultrasound propulsion enhances therapeutic delivery of antioxidant nanocarriers in osteoarthritis, indicating improved penetration and ROS-scavenging effects.
Osteoarthritis is a major global health concern, characterized by progressive degradation of articular cartilage and excessive accumulation of reactive oxygen species (ROS). Although intra‐articular drug delivery is a commonly employed therapeutic approach, its effectiveness is often hindered by the dense and avascular structure of the cartilage matrix. To overcome this limitation, ultrasound‐propelled MnO 2 ‐decorated nanobowls (Mn‐nanobowls) are developed, capable of directional movement within joint tissues. These nanobowls are synthesized via self‐assembly of P(AzoAA 24 ‐ stat ‐MAA 10 ), facilitated by π – π interactions and hydrogen bonding, followed by in situ deposition of MnO 2 nanoparticles onto their surface. The MnO 2 decoration endows nanobowls with ROS‐scavenging properties and simultaneous oxygen generation. Furthermore, the Mn‐nanobowls exhibit strong catalase‐like enzymatic activity, achieving ≈25% hydrogen peroxide decomposition at a MnO 2 concentration of 5 µg mL −1 , comparable to that of free MnO 2 particles. Under ultrasound irradiation, the Mn‐nanobowls demonstrate directional propulsion at a speed of 40.35 µm s −1 in vitro. In vivo studies indicate that ultrasound‐propelled Mn‐nanobowls can penetrate deeply into the dense cartilage matrix, up to 307 µm, substantially improving therapeutic delivery compared to passive diffusion. Overall, this study introduces a promising and innovative strategy for osteoarthritis treatment through ultrasound‐propelled nanocarriers with enhanced tissue penetration and multifunctional ROS‐scavenging capabilities.
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Gong et al. (2025) studied this question.
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