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- Title
Copper(II) Pyridyl Aminophenolates: Hypoxia‐Selective, Nucleus‐Targeting Cytotoxins, and Magnetic Resonance Probes.
- Authors
Prosser, Kathleen E.; Xie, Da; Chu, Annica; MacNeil, Gregory A.; Varju, Bryton R.; Kadakia, Rahul T.; Que, Emily L.; Walsby, Charles J.
- Abstract
Targeting the low‐oxygen (hypoxic) environments found in many tumours by using redox‐active metal complexes is a strategy that can enhance efficacy and reduce the side effects of chemotherapies. We have developed a series of CuII complexes with tridentate pyridine aminophenolate‐based ligands for preferential activation in the reduction window provided by hypoxic tissues. Furthermore, ligand functionalization with a pendant CF3 group provides a 19F spectroscopic handle for magnetic‐resonance studies of redox processes at the metal centre and behaviour in cellular environments. The phenol group in the ligand backbone was substituted at the para position with H, Cl, and NO2 to modulate the reduction potential of the CuII centre, giving a range of values below the window expected for hypoxic tissues. The NO2‐substituted complex, which has the highest reduction potential, showed enhanced cytotoxic selectivity towards HeLa cells grown under hypoxic conditions. Cell death occurs by apoptosis, as determined by analysis of the cell morphology. A combination of 19F NMR and ICP‐OES indicates localization of the NO2 complex in HeLa cell nuclei and increased cellular accumulation under hypoxia. This correlates with DNA nuclease activity being the likely origin of cytotoxic activity, as demonstrated by cleavage of DNA plasmids in the presence of the CuII nitro complex and a reducing agent. Selective detection of the paramagnetic CuII complexes and their diamagnetic ligands by 19F MRI suggests hypoxia‐targeting theranostic applications by redox activation.
- Subjects
MAGNETIC resonance; CYTOTOXINS; CELL morphology; MAGNETIC resonance imaging; CELL analysis; CELL death; HELA cells
- Publication
Chemistry - A European Journal, 2021, Vol 27, Issue 38, p9839
- ISSN
0947-6539
- Publication type
Academic Journal
- DOI
10.1002/chem.202100603