Tumor Reoxygenation and Blood Perfusion Enhanced Photodynamic Therapy using Ultrathin Graphdiyne Oxide Nanosheets.
Wei JiangZhen ZhangQin WangJiaxiang DouYangyang ZhaoYin-Chu MaHuarong LiuHangxun XuYu-Cai WangPublished in: Nano letters (2019)
Both diffusion-limited and perfusion-limited hypoxia are associated with tumor progression, metastasis, and the resistance to therapeutic modalities. A strategy that can efficiently overcome both types of hypoxia to enhance the efficacy of cancer treatment has not been reported yet. Here, it is shown that by using biomimetic ultrathin graphdiyne oxide (GDYO) nanosheets, both types of hypoxia can be simultaneously addressed toward an ideal photodynamic therapy (PDT). The GDYO nanosheets, which are oxidized and exfoliated from graphdiyne (GDY), are able to efficiently catalyze water oxidation to release O2 and generate singlet oxygen (1O2) using near-infrared irradiation. Meanwhile, GDYO nanosheets also exhibit excellent light-to-heat conversion performance with a photothermal conversion efficiency of 60.8%. Thus, after the GDYO nanosheets are coated with iRGD peptide-modified red blood membrane (i-RBM) to achieve tumor targeting, the biomimetic GDYO@i-RBM nanosheets can simultaneously enhance tumor reoxygenation and blood perfusion for PDT. This study provides new insights into utilizing novel water-splitting materials to relieve both diffusion- and perfusion-limited hypoxia for the development of a novel therapeutic platform.
Keyphrases
- photodynamic therapy
- metal organic framework
- reduced graphene oxide
- quantum dots
- highly efficient
- visible light
- fluorescence imaging
- endothelial cells
- contrast enhanced
- transition metal
- gold nanoparticles
- magnetic resonance imaging
- cancer therapy
- poor prognosis
- computed tomography
- induced apoptosis
- nitric oxide
- high throughput
- long non coding rna
- radiation induced
- tissue engineering