2D Copper(II) Metalated Metal-Organic Framework Nanocomplexes for Dual-enhanced Photodynamic Therapy and Amplified Antitumor Immunity.
Zixuan ChenYafeng WuZhipeng YaoJuan SuZhi WangHongping XiaSong-Qin LiuPublished in: ACS applied materials & interfaces (2022)
The immunosuppressive tumor microenvironment (TME) poses tremendous challenges for efficient immunotherapy. Smart nanomedicine is designed to modulate immunosuppressive TMEs based on the combination of dual-enhanced photodynamic therapy (PDT) triggered immunogenic cell death (ICD) and relieved hypoxic microenvironment. Copper(II) metalated metal-organic framework nanosheets (Cu-TCPP(Al)) are the foundation of the nanomedicine, and platinum nanoparticles (Pt NPs) and folate are subsequently introduced onto the Cu-TCPP(Al) surface (Cu-TCPP(Al)-Pt-FA). Upon targeted cellular uptake, intracellular GSH concentration is decreased because of the specific adsorption between GSH and Cu II ; meanwhile, Pt NPs possess catalase-like activity, which can continuously depose intracellular H 2 O 2 to O 2 to alleviate the hypoxic TME. The two factors synergistically improve the ROS concentration for dual-enhanced PDT. The highly toxic ROS can correspondingly cause amplified oxidative stress and then trigger the ICD. The ICD process stimulates antigen-presenting cells and activates the systemic antitumor immune response. Furthermore, the relieved hypoxic TME increases the infiltration of cytotoxic T lymphocytes (CTLs) at the tumor site, which can promote the transformation of the immunosuppressive M2 macrophage to immunoactive M1 phenotype. The easily prepared yet versatile nanomedicine possesses an excellent antitumor effect with the cooperation of dual-enhanced PDT and immunotherapy.
Keyphrases
- metal organic framework
- photodynamic therapy
- cell death
- fluorescence imaging
- cancer therapy
- immune response
- oxidative stress
- cell cycle arrest
- reactive oxygen species
- induced apoptosis
- dna damage
- oxide nanoparticles
- stem cells
- adipose tissue
- aqueous solution
- toll like receptor
- dendritic cells
- drug delivery
- cell proliferation
- gold nanoparticles
- case report
- endoplasmic reticulum stress
- inflammatory response
- drug induced
- highly efficient