Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan, Republic of China.
Department of Chemical and Materials Engineering, National Yunlin University of Science and Technology, Yunlin 64002, Taiwan, Republic of China.
ACS Appl Bio Mater. 2021 Jul 19;4(7):5650-5660. doi: 10.1021/acsabm.1c00452. Epub 2021 Jun 16.
Combining phototherapy with the cancer cell metabolic pathway altering strategies, that is, glucose starvation, would be a promising approach to accomplish high curative efficiency of cancer treatment. Accordingly, herein, we sought to construct a multifunctional biomimetic hybrid nanoreactor by fastening nanozyme AuNPs (glucose oxidase activity) and PtNPs (catalase and peroxidase activity) and photosensitizer Indocyanine green (ICG) onto the polydopamine (PDA) surface (ICG/Au/Pt@PDA-PEG) to attain superior cancer cell killing efficiency though win-win cooperation between starvation therapy, phototherapy, and chemodynamic therapy. The as-synthesized ICG/Au/Pt@PDA-PEG has shown excellent light-to-heat conversion (photothermal therapy) and reactive oxygen species generation (photodynamic therapy) properties upon laser irradiation and also red-shifted ICG absorption (from 780 to 800 nm) and enhanced its photostability. Further, the ICG/Au/Pt@PDA-PEG NRs have reduced the solution glucose concentration and slightly increased solution oxygen levels and also enhanced 3,3',5,5'-tetramethylbenzidine oxidation in the presence of glucose through a cascade of enzymatic activities. The results demonstrated that the ICG/Au/Pt@PDA-PEG NRs have superior therapeutic efficacy against cancer cells the cooperative effect between starvation/photo/chemodynamic therapies and not much toxicity to normal cells.
将光疗与改变癌细胞代谢途径的策略(即葡萄糖饥饿)相结合,将是实现癌症治疗高疗效的有前途的方法。因此,在这里,我们试图通过将纳米酶 AuNPs(葡萄糖氧化酶活性)和 PtNPs(过氧化氢酶和过氧化物酶活性)和光敏剂吲哚菁绿(ICG)固定到聚多巴胺(PDA)表面(ICG/Au/Pt@PDA-PEG)上来构建多功能仿生杂化纳米反应器,以通过饥饿疗法、光疗和化学动力学疗法的双赢合作实现卓越的癌细胞杀伤效率。所合成的 ICG/Au/Pt@PDA-PEG 在激光照射下表现出优异的光热转换(光热疗法)和活性氧生成(光动力疗法)性能,并且 ICG 吸收红移(从 780nm 到 800nm),并增强其光稳定性。此外,ICG/Au/Pt@PDA-PEG NRs 在葡萄糖存在下通过级联酶活性降低了溶液葡萄糖浓度,略微增加了溶液氧水平,并增强了 3,3',5,5'-四甲基联苯胺的氧化。结果表明,ICG/Au/Pt@PDA-PEG NRs 对癌细胞具有优异的治疗效果,饥饿/光/化学动力学治疗的协同作用对正常细胞的毒性不大。