Abstract
Nalidixic acid was the first quinolone introduced in 1962. Structural changes have resulted in an extended spectrum and better pharmacokinetics profile. All agents have an N-1-substituted 1,4-dihydro-4-oxopyridine-3-carboxylic acid as the basic nucleus. The fluorinated 4-quinolones, such as ciprofloxacin, moxifloxacin, and levofloxacin are effective for treatment of a wide variety of infectious diseases. Potentially life threatening and rare side effects detected by postmarketing surveillance resulted in the withdrawal of gatifloxacin (hypoglycemia), trovafloxacin (hepatotoxicity), sparfloxacin (QTc prolongation, phototoxicity), temafloxacin (hemolytic anemia), grepafloxacin (cardiotoxicity), and clinafloxacin (phototoxicity) from the US market. Commercially available fluorinated quinolones available in the USA are widely used by clinicians (Fig. 12.1).
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Further Reading
Leibovitz, E. (2006). The use of fluoroquinolones in children. Curr Opin Pediatr, 18(1), 64–70.
O’Donnell, J. A., & Gelone, S. P. (2000). Fluoroquinolones. Infect Dis Clin North Am, 14(2), 489–513, xi.
O’Donnell, J. A., & Gelone, S. P. (2004). The newer fluoroquinolones. Infect Dis Clin North Am, 18(3), 691–716, x.
Walker, R. C. (1999). The fluoroquinolones. Mayo Clin Proc, 74(10), 1030–1037.
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Finberg, R.W., Guharoy, R. (2012). Quinolones. In: Clinical Use of Anti-infective Agents. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-1068-3_12
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DOI: https://doi.org/10.1007/978-1-4614-1068-3_12
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