One-Step Integration of Tumor Microenvironment-Responsive Calcium and Copper Peroxides Nanocomposite for Enhanced Chemodynamic/Ion-Interference Therapy.
Bin LiuYulong BianShuang LiangMeng YuanShuming DongLili FengShili GaiPiaoping YangZiyong ChengJun LinPublished in: ACS nano (2021)
Recently, various metal peroxide nanomaterials have drawn increasing attention as an efficient hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) self-supplying agent for enhanced tumor therapy. However, a single kind of metal peroxide is insufficient to achieve more effective antitumor performance. Here, a hyaluronic acid modified calcium and copper peroxides nanocomposite has been synthesized by a simple one-step strategy. After effective accumulation at the tumor site due to the enhanced permeability and retention (EPR) effect and specific recognition of hyaluronate acid with CD44 protein on the surface of tumor cells, plenty of Ca<sup>2+</sup>, Cu<sup>2+</sup>, and H<sub>2</sub>O<sub>2</sub> can be simultaneously released in acid and hyaluronidase overexpressed tumor microenvironment (TME), generating abundant hydroxyl radical through enhanced Fenton-type reaction between Cu<sup>2+</sup> and self-supplying H<sub>2</sub>O<sub>2</sub> with the assistance of glutathione depletion. Overloaded Ca<sup>2+</sup> can lead to mitochondria injury and thus enhance the oxidative stress in tumor cells. Moreover, an unbalanced calcium transport channel caused by oxidative stress can further promote tumor calcification and necrosis, which is generally defined as ion-interference therapy. As a result, the synergistic effect of Fenton-like reaction by Cu<sup>2+</sup> and mitochondria dysfunction by Ca<sup>2+</sup> in ROS generation is performed. Therefore, a TME-responsive calcium and copper peroxides nanocomposite based on one-step integration has been successfully established and exhibits a more satisfactory antitumor efficiency than any single kind of metal peroxide.
Keyphrases
- hydrogen peroxide
- oxidative stress
- hyaluronic acid
- cell death
- dna damage
- aqueous solution
- nitric oxide
- reduced graphene oxide
- reactive oxygen species
- wastewater treatment
- oxide nanoparticles
- quantum dots
- stem cells
- diabetic rats
- ischemia reperfusion injury
- gold nanoparticles
- bone marrow
- endothelial cells
- mesenchymal stem cells
- metal organic framework
- induced apoptosis
- binding protein
- small molecule
- endoplasmic reticulum stress
- replacement therapy
- recombinant human