Both the fluoroquinolones and the beta-lactam antibiotics are bactericidal in action. But they work through different mechanism of action. Fluroquinolones are bacterial nucleic acid inhibitor whereas cephalosporins are bacterial cell wall synthesis inhibitor. Their main purpose is to eradicate any bacterial infection by killing the bacteria that is termed as bactericidal action. Being bactericidal their action depends on two different parameters-

I. Action of Cephalosporins depends on how long they remain on plasma above the MIC (Time dependent)

II. Action of Fluoroquinolones depends on what extent of drug in available within the tissue (Concentration dependent)

Why they differ on these two parameters, is there any biochemical factor(s) responsible for their nature of action?

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