A New Sono‐Chemo Sensitizer Overcoming Tumor Hypoxia for Augmented Sono/Chemo‐Dynamic Therapy and Robust Immune‐Activating Response. Issue 10 (22nd December 2022)

• Record Type: Journal Article
• Authors: Sun, Luyao; Gao, Wendong; Wang, Jingjing; Niu, Xueming; Kurniawan, Nyoman; Li, Li; Xu, Zhi Ping
• Is Part Of: Small. Volume 19:Issue 10(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-12-22
• Subjects: chemodynamic therapy -- layered double hydroxides -- sono‐chemo sensitizers -- sonodynamic therapy -- tumor‐associated macrophage polarization; Nanotechnology -- Periodicals; Nanoparticles -- Periodicals; Microtechnology -- Periodicals; 620.5
• DOI: 10.1002/smll.202206078
• Languages: English
• ISSNs: 1613-6810

Abstract

Abstract: Novel sonosensitizers with intrinsic characteristics for tumor diagnosis, efficient therapy, and tumor microenvironment regulation are appealing in current sonodynamic therapy. Herein, a manganese (Mn)‐layered double hydroxide‐based defect‐rich nanoplatform is presented as a new type of sono‐chemo sensitizer, which allows ultrasound to efficiently trigger reactive oxygen species generation for enhanced sono/chemo‐dynamic therapy. Moreover, such a nanoplatform is able to relieve tumor hypoxia and achieve augmented singlet oxygen production via catalyzing endogenous H2 O2 into O2 . On top of these actions, the released Mn 2+ ions and immune‐modulating agent significantly intensify immune activation and reverse the immunosuppressive tumor microenvironment to the immunocompetent one. Consequently, this nanoplatform exhibits excellent anti‐tumor efficacy and effectively suppresses both primary and distant tumor growth, demonstrating a new strategy to functionalize nanoparticles as sono‐chemo sensitizers for synergistic combination cancer therapy. Abstract : An Mn‐layered double hydroxide‐based sono‐chemo sensitizer loaded with vadimezan is devised with three functions in the tumor microenvironment—O2 generation from H2 O2 by MnO2 to relieve hypoxia, augmented reactive oxygen species production under ultrasound to induce tumor cell apoptosis, and synergized cytokine release to elicit anti‐tumor immunity. These functions together inhibit both primary and distant tumor growth under ultrasound.