Journal
DALTON TRANSACTIONS
Volume 46, Issue 34, Pages 11395-11407Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7dt02273e
Keywords
-
Categories
Funding
- National Natural Science Foundation of China [21231007, 21572282, 21571196]
- 973 program [2014CB845604, 2015CB856301]
- Guangdong Natural Science Foundation [2015A030306023]
- Fundamental Research Funds for the Central Universities
Ask authors/readers for more resources
Many phosphorescent iridium complexes are potent candidates as photodynamic therapeutic agents. In this work, a series of mixed-ligand phosphorescent iridium complexes (Ir1: [Ir(L-1)(bpy)Cl](PF6)(2); Ir2: [Ir(L-1)(ppy)Cl](PF6); Ir3: [Ir(L-2)(bpy)Cl](PF6)(2); Ir4: [Ir(L-2)(ppy)Cl](P(F)6). L1 = 2,6-bis(2-benzimidazolyl) pyridine; bpy = 2,2'-bipyridine; L-2 = 2,6-bis(1-methyl-benzimidazol-2-yl)pyridine; ppy = 2-phenylpyridine) have been synthesized and characterized. These complexes display high luminescence quantum yields and long phosphorescence lifetimes. All the complexes are resistant to hydrolysis in aqueous solutions, and can produce singlet oxygen (O-1(2)) effectively upon irradiation. Ir1 and Ir2 show pH-sensitive emission properties. Interestingly, higher cellular uptake efficiency is observed for Ir2 and Ir4 with the cyclometalated ppy ligand in human lung adenocarcinoma A549 cells. Ir2 with pH-sensitive emission properties can selectively image lysosomes, and Ir4 can specifically target mitochondria. Both Ir2 and Ir4 exhibit potent photodynamic therapy (PDT) effects, with Ir2 displaying a higher phototoxicity index (PI) especially in A549 cells (PI > 54). Mechanism studies indicate that Ir2 and Ir4 can induce apoptosis through reactive oxygen species (ROS) generation and caspase activation upon visible light (425 nm) irradiation. As expected, Ir2 can damage lysosomes more effectively with a pH-sensitive singlet oxygen (O-1(2)) yield, while Ir4 tends to impair mitochondrial function. Nevertheless, the practical application of Ir2 and Ir4 for PDT may be limited to superficial tumors due to the short excitation wavelength (425 nm). Our study gives insights into the design and anticancer mechanisms of new metal-based PDT anticancer agents.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available