Abstract
Cellular uptake, luminescence imaging and antimicrobial activity against clinically relevant methicillin-resistant S. aureus (MRSA) bacteria are reported. The osmium(ii) complexes [Os(N^N)3]2+ (N^N = 1-benzyl-4-(pyrid-2-yl)-1,2,3-triazole (12+); 1-benzyl-4-(pyrimidin-2-yl)-1,2,3-triazole (22+); 1-benzyl-4-(pyrazin-2-yl)-1,2,3-triazole (32+)) were prepared and isolated as the chloride salts of their meridional and facial isomers. The complexes display prominent spin-forbidden ground state to triplet metal-to-ligand charge transfer (3MLCT) state absorption bands enabling excitation as low as 600 nm for fac/mer-32+ and observation of emission in aqueous solution in the deep-red/near-IR regions of the spectrum. Cellular uptake studies within MRSA cells show antimicrobial activity for 12+ and 22+ with greater toxicity for the meridional isomers in each case and mer-12+ showing the greatest potency (32 μg mL-1 in defined minimal media). Super-resolution imaging experiments demonstrate binding of mer-and fac-12+ to bacterial DNA with high Pearson's colocalisation coefficients (up to 0.95 using DAPI). Phototoxicity studies showed the complexes exhibited a higher antimicrobial activity upon irradiation with light.
Original language | English |
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Pages (from-to) | 8928-8935 |
Number of pages | 8 |
Journal | Chemical Science |
Volume | 11 |
Issue number | 33 |
Early online date | 7 Aug 2020 |
DOIs | |
Publication status | Published - 7 Sep 2020 |
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Paul Elliott
- Department of Physical and Life Sciences - Professor
- School of Applied Sciences
- Centre for Functional Materials - Director
- Chemical Synthesis and Design Centre - Associate Member
- Pharmacology and Therapeutics Centre - Associate Member
Person: Academic