European Journal of Clinical Pharmacology

, Volume 35, Issue 2, pp 161–165 | Cite as

Effects of enoxacin, ofloxacin and norfloxacin on theophylline disposition in humans

  • M. Sano
  • K. Kawakatsu
  • C. Ohkita
  • I. Yamamoto
  • M. Takeyama
  • H. Yamashina
  • M. Goto
Originals

Summary

The effect of three new fluoroquinolones on theophylline kinetics and the urinary excretion of metabolites was studied in 5 healthy subjects (3 male, 2 female).

All subjects received serial, single i.v. infusions of theophylline (aminophylline, 250 mg) over 60 min after 200 mg doses of a quinolone (enoxacin, ofloxacin, norfloxacin) every 8 h for 3 consecutive days, the quinolone being administered up to the day following theophylline administration.

Pretreatment with ofloxacin and norfloxacin did not influence theophylline disposition, but theophylline clearance fell from 0.054 to 0.027 l·h−1·kg−1 in the presence of enoxacin, without a change in the apparent volume of distribution. Enoxacin, too, was the sole compound to increase the urinary excretion of theophylline (33.2 vs 43.9 mg, before vs after treatment), and significantly to decrease the excretion of 3-methylxanthine (3-MX), 1-methyluric acid (1-MU) and 1,3-dimethyluric acid (1,3-DMU) in 24-h urine samples (from 19.8 to 7.16 mg, from 28.3 to 10.3 mg and from 68.8 to 49.5 mg, respectively). The effect of the quinolones on hepatic drug metabolizing enzyme activity was investigated in each subject using the ratios of 6-hydroxycortisol to total 17-hydroxycorticosteroids and to free cortisol in 24-h urines as an index of the hepatic P-450-dependent enzyme system. No significant difference in ratio was observed between control and other treatments. It is concluded that the theophylline-enoxacin interaction was largely due to inhibition of a metabolic system other than the common hepatic P-450 system.

Key words

theophylline enoxacin ofloxacin norfloxacin drug metabolism/interaction hepatic P-450 

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Copyright information

© Springer-Verlag 1988

Authors and Affiliations

  • M. Sano
    • 1
  • K. Kawakatsu
    • 2
  • C. Ohkita
    • 1
  • I. Yamamoto
    • 1
  • M. Takeyama
    • 2
  • H. Yamashina
    • 1
  • M. Goto
    • 3
  1. 1.Department of Hospital PharmacyTenri HospitalNaraJapan
  2. 2.Department of Hospital Pharmacy, Chest Disease Research InstituteKyoto UniversityKyotoJapan
  3. 3.Department of Hospital PharmacyNagoya Memorial HospitalNagoyaJapan

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