Volume 83, Issue 4 pp. 463-467
Research Article

Photodegradation of some quinolones used as antimicrobial therapeutics

Eva-Maria Tiefenbacher

Eva-Maria Tiefenbacher

Walther-Straub Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University, Nussbaumstr. 26, D-80336 Munich, Germany

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Ekkehard Haen

Ekkehard Haen

Walther-Straub Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University, Nussbaumstr. 26, D-80336 Munich, Germany

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Bernhard Przybilla

Bernhard Przybilla

Department of Dermatology, Ludwig-Maximilians-University, Frauenlobstr. 9-11, D-80337 Munich, Germany

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Hermann Kurz

Hermann Kurz

Walther-Straub Institute of Pharmacology and Toxicology, Ludwig-Maximilians-University, Nussbaumstr. 26, D-80336 Munich, Germany

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First published: April 1994
Citations: 6

Abstract

The photostability of the fluoroquinolones ciprofloxacin (CPX), ofloxacin (OFX), and fleroxacin (FLX) toward ultraviolet irradiation (UVA) and room light was investigated in dilute aqueous solutions. A series of photoproducts was observed by high-performance liquid chromatography (HPLC) for all three drugs. As little as 1 h of exposure to room light was enough for the formation of detectable amounts of CPX photoproducts. The major CPX photoproduct was characterized as a dimer by liquid secondary ion mass spectrometry, but its structure was not determined. Since irradiation of CPX results (as cited in ref/11) in a loss of antibacterial activity and since all substances, parent drugs as well as their photoproducts, are potential candidates for undesired drug effects, quinolone drugs should be strictly protected from all light during storage and administration.

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