Summary
Despite some limited differences in pharmacokinetic parameters among the newer quinolones, their pharmacology is characterised by high volumes of distribution, long elimination half-lives, good to excellent bioavailability, low protein binding, limited biotransformation and different elimination pathways (mainly through the kidneys). The unique aspects of quinolones in comparison with β-lactams and aminoglycosides are their higher volumes of distribution, longer elimination half-lives and their intracellular high concentration, especially in phagocytic cells.
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Lode, H., Höffken, G., Borner, K. et al. Unique Aspects of Quinolone Pharmacokinetics. Clin-Pharmacokinet 16 (Suppl 1), 1–4 (1989). https://doi.org/10.2165/00003088-198900161-00003
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DOI: https://doi.org/10.2165/00003088-198900161-00003