Enhanced cellular uptake and photochemotherapeutic potential of a lipophilic strained Ru(ii) polypyridyl complex. Issue 30 (3rd June 2019)

• Record Type: Journal Article
• Authors: Mehanna, Stephanie; Mansour, Najwa; Audi, Hassib; Bodman-Smith, Kikki; Mroueh, Mohamad A.; Taleb, Robin I.; Daher, Costantine F.; Khnayzer, Rony S.
• Is Part Of: RSC advances. Volume 9:Issue 30(2019)
• Page Start: 17254
• Page End: 17265
• Publication Date: 2019-06-03
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c9ra02615k
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : A strained Ru(ii ) prodrug exhibited enhanced cellular uptake and phototoxicity due to its lipophilic properties. Abstract : The use of ruthenium complexes as chemotherapeutic agents has been recently explored as one of the alternatives to conventional treatments. In the present study, two Ru(ii ) polypyridyl complexes were synthesized and characterized: a strained [Ru(bipy)2 (BC)]Cl2 (complex1 ) where [bipy = 2, 2′-bipyridine and BC = bathocuproine] along with the unstrained control [Ru(bipy)2 (phen)]Cl2 (complex2 ) where [phen = 1, 10-phenanthroline]. The photophysical and photochemical analyses proved that unlike the photostable complex2, complex1 ejected both bipy and BC ligands at a ratio of 3 : 1 respectively. Results showed that the activity of complex1 was significantly enhanced upon photoactivation. The response was however particularly significant in B16-F10 melanoma cells where phototoxicity index (PI = IC50 dark/IC50 light) was >900. When compared to cisplatin, the photoproducts were more potent against all tested cell lines, implying that the complex acquired significant chemotherapeutic potential upon irradiation. Cellular uptake of complex1 and the free BC ligand were found to be significantly facilitated as evidenced by 400–600 fold increase in concentration of the compounds inside the cells relative to the extracellular culture medium. Complex2 exhibited 35 times lower cellular concentration relative to complex1 . Flow cytometry and plasmid DNA gel electrophoresis measurements showed that complex1 interacts with DNA inducing apoptosis in the dark and either late-apoptosis or necrosis upon irradiation. These findings corroborate the importance of lipophilic ligands such as BC to enhance uptake and subsequently improve the photochemotherapy potential of Ru(ii ) polypyridyl complexes.