Macrophage-Targeted Sonodynamic/Photothermal Synergistic Therapy for Preventing Atherosclerotic Plaque Progression Using CuS/TiO 2 Heterostructured Nanosheets.
Zhengyu CaoGuotao YuanLingli ZengLu BaiXiao LiuMaoxiong WuRunlu SunZhiteng ChenYuan JiangQingyuan GaoYangxin ChenYuling ZhangYue PanJing-Feng WangPublished in: ACS nano (2022)
Sonodynamic therapy (SDT) and photothermal therapy (PTT) are two effective strategies for the treatment of atherosclerotic plaques. However, the low yield of reactive oxygen species (ROS) of conventional organic sonosensitizers and the low biosafety of hyperthermia limit the therapeutic efficacy of SDT and PTT. Herein, we report copper sulfide/titanium oxide heterostructure nanosheets modified with hyaluronic acid (HA) and PEG (HA-HNSs) for low-intensity sonodynamic and mild-photothermal synergistic therapy for early atherosclerotic plaques. CuS/TiO 2 heterostructure nanosheets (HNSs) show high electron-hole separation efficiency and superior sonodynamic performance, because it has high surface energy crystal facets as well as a narrow band. Moreover, HNSs exhibit intense absorbance in the NIR-II region, which endows the nanosheets with excellent photothermal performance. With a further modification of HA, HA-HNSs can selectively target intraplaque proinflammatory macrophages through CD44-HA interaction. Because SDT reduces the expression of heat shock protein 90 and PTT facilitates the sonocatalytic process, the combination of SDT and PTT based on HA-HNSs could synergistically induce proinflammatory macrophage apoptosis. More importantly, the synergistic therapy prevents the progression of early atherosclerotic plaque by removing lesional macrophages and mitigating inflammation. Taken together, this work provides a macrophage-targeting sonodynamic/photothermal synergistic therapy, which is an effective translational clinical intervention for early atherosclerotic plaques.
Keyphrases
- cancer therapy
- drug delivery
- quantum dots
- photodynamic therapy
- heat shock protein
- reactive oxygen species
- hyaluronic acid
- reduced graphene oxide
- drug release
- visible light
- oxidative stress
- adipose tissue
- randomized controlled trial
- coronary artery disease
- metal organic framework
- highly efficient
- dna damage
- mouse model
- gold nanoparticles
- long non coding rna
- bone marrow
- binding protein
- heat shock
- fluorescent probe