Multiple Functions Integrated inside a Single Molecule for Amplification of Photodynamic Therapy Activity.
Xianqing ShiQichen ZhanYanqing LiLin ZhouShaohua WeiPublished in: Molecular pharmaceutics (2019)
Nitric oxide (NO) can play both prosurvival and prodeath roles in photodynamic therapy (PDT). The generation efficiency of peroxynitrite anions (ONOO-), by NO and superoxide anions (O2•-), significantly influenced the outcome. Reports indicated that such efficiency is closely related to the distance between NO and O2•-. Thus, in this manuscript, l-arginine (Arg) ethyl ester-modified zinc phthalocyanine (Arg-ZnPc) was designed and synthesized as a photosensitizer (PS) and NO donor. Post light irradiation, the guanido of Arg-ZnPc can be effectively oxidized by the generated reactive oxygen species (ROS) in the PDT process to release NO. Such a strategy could ensure O2•- and NO generation in the same place at the same time to guarantee effective ONOO- formation. In addition, NO has other multiple synergistic cancer treatment functions, including tumor tissue vasodilatation for drug extravasation promotion, P-glycoprotein (P-gp) downregulation for drug efflux inhibition, and glutathione depletion for cancer cell endogenous antioxidant defense destruction. In vitro and in vivo results indicated that the effective ONOO- formation and multiple functions of Arg-ZnPc could synergistically enhance its PDT activity and ensure satisfactory cancer treatment outcome.
Keyphrases
- photodynamic therapy
- single molecule
- nitric oxide
- reactive oxygen species
- fluorescence imaging
- ionic liquid
- living cells
- adverse drug
- hydrogen peroxide
- signaling pathway
- oxidative stress
- cell death
- cell proliferation
- drug induced
- papillary thyroid
- squamous cell carcinoma
- fluorescent probe
- young adults
- squamous cell
- radiation induced
- oxide nanoparticles
- innate immune
- drug delivery
- cancer therapy
- low density lipoprotein