International Journal of Gynecology & Obstetrics
Volume 102, Issue 2 , Pages 132-136, August 2008

Penetration and accumulation of moxifloxacin in uterine tissue

  • Heino Stass

      Affiliations

    • Bayer HealthCare AG, Wuppertal, Germany
    • Corresponding Author InformationCorresponding author. Bayer HealthCare AG, Clinical Pharmacology, Bldg. 470, Room 219, D-42096 Wuppertal, Germany. Tel.: +49 202 36 4289; fax: +49 202 36 8998.
  • ,
  • Dagmar Kubitza

      Affiliations

    • Bayer HealthCare AG, Wuppertal, Germany
  • ,
  • Baybur Aydeniz

      Affiliations

    • University Women's Clinic, Tübingen, Germany
  • ,
  • Deithelm Wallwiener

      Affiliations

    • University Women's Clinic, Tübingen, Germany
  • ,
  • Atef Halabi

      Affiliations

    • CRS-Kiel GmbH, Kiel, Germany
  • ,
  • Christoph Gleiter

      Affiliations

    • CenTrial GmbH, Tübingen, Germany

Received 24 January 2008; received in revised form 29 February 2008; accepted 29 February 2008. published online 12 May 2008.

Abstract 

Objective

To determine whether moxifloxacin penetrates the uterine tissue and accumulates at levels sufficient to eradicate the major pathogens causing pelvic inflammatory disease (PID).

Method

In a prospective, multicenter, open-label, parallel-group study we determined the concentration of moxifloxacin in plasma and uterine tissue after a single, 400-mg intravenous dose of moxifloxacin. Study participants were randomized for time of tissue sampling, which was performed 1, 2, 4, 7, or 24 hours following the moxifloxacin infusion.

Results

Of 43 participants, 40 were randomized to tissue sampling. Moxifloxacin accumulated in uterine tissue and concentrations were highest 1 hour after infusion in both plasma and tissue. Tissue to plasma ratios remained between 1.7 and 2.1 for 24 hours. Moxifloxacin was found to be safe and well tolerated.

Conclusion

Based on known minimum inhibitory concentration data, the uterine tissue concentrations of moxifloxacin achieved over 24 hours would be sufficient to eradicate the range of bacterial pathogens responsible for PID.

Keywords: Moxifloxacin, Pelvic inflammatory disease, Pharmacokinetics, Uterine tissue

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0020-7292(08)00151-3

doi:10.1016/j.ijgo.2008.02.020

International Journal of Gynecology & Obstetrics
Volume 102, Issue 2 , Pages 132-136, August 2008