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. 2023 Feb 8;7(3):202–224. doi: 10.1038/s41570-023-00463-4

Fig. 8. Metal complexes for imaging bacterial infections.

Fig. 8

A, Structures of imaging agents. B, The structure of [68Ga]-PVD-PAO1 (Ba) and static PET–CT imaging of [68Ga]-PVD-PAO1 (Bb and Bc) compared with [68Ga]-citrate (Bd) and [18F]-FDG (Be) in a mouse muscle-infection model 45 min post-injection of Pseudomonas aeruginosa in one thigh and Escherichia coli or sterile inflammation in the other thigh. C, The structure of [68Ga]-DFO-B (Ca) and static PET–CT imaging of [68Ga]-DFO-B in a mouse thigh-infection model 45 min post-injection with P. aeruginosa (Cb) or Staphylococcus aureus (Cc) (yellow arrows indicate site of infection). PET, positron-emission tomography; CT, computed tomography; PAI, P. aeruginosa infection; ECI, E. coli infection; SI, sterile inflammation; TAFC, triacetylfusarinine; FOXE, ferrioxamine E; PVD, pyoverdine; FDG, fluorodeoxyglucose; DFO-B, desferrioxamine-B; ID g−1, injected dose per gram of tissue; kBq ml−1, kilobecquerel per millilitre. Part B reprinted from ref. 267, under a Creative Commons licence CC-BY 4.0. Part C reprinted from ref. 268, under a Creative Commons licence CC-BY 4.0.