Key Laboratory of Molecular Biophysics, Hebei Province, Institute of Biophysics, School of Sciences, Hebei University of Technology, Tianjin, China; State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, China.
State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, China.
Nanomedicine. 2021 Oct;37:102440. doi: 10.1016/j.nano.2021.102440. Epub 2021 Jul 10.
Lately, chemotherapy and photodynamic therapy (PDT) synergistic therapy has become a promising anti-cancer treatment mean. However, the hypoxia in tumor leads to huge impediments to the oxygen-dependent PDT effects. In this work, a multifunctional nanoplatform (TUDMP) based on a multivariable porphyrin-nMOFs core and a manganese dioxide (MnO) shell was prepared for relieving tumor hypoxia and enhancing chemo-photodynamic synergistic therapy performance. The obtained TUDMP nanoplatform could effectively catalyze the hydrolysis of hydrogen peroxide to generate oxygen and also lead to consumption of antioxidant GSH, thereby facilitating the production of cytotoxic reactive oxygen species (ROS) by photosensitizer under laser irradiation. More importantly, the decomposition of the MnO shell would further promote the release of the loaded doxorubicin (DOX), and thus an efficient chemo-PDT synergistic therapy was realized. Both in vitro and in vivo experimental results demonstrated the oxygen self-sufficient multifunctional nanoplatform could exhibit significantly enhanced anticancer efficiencies compared with chemotherapy or PDT alone.
最近,化疗和光动力疗法(PDT)协同治疗已成为一种很有前途的抗癌治疗手段。然而,肿瘤中的缺氧会极大地阻碍依赖氧的 PDT 效果。在这项工作中,基于多变量卟啉-nMOFs 核和二氧化锰(MnO)壳的多功能纳米平台(TUDMP)被制备用于缓解肿瘤缺氧并增强化疗-光动力协同治疗性能。所获得的 TUDMP 纳米平台可以有效地催化过氧化氢的水解以产生氧气,并且还会导致抗氧化剂 GSH 的消耗,从而有利于在激光照射下通过光敏剂产生细胞毒性活性氧(ROS)。更重要的是,MnO 壳的分解会进一步促进负载的阿霉素(DOX)的释放,从而实现有效的化疗-PDT 协同治疗。体外和体内实验结果表明,与单独的化疗或 PDT 相比,具有自供氧功能的多功能纳米平台可以表现出显著增强的抗癌效率。
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