Clearance of intravitreal moxifloxacin

Mohan N Iyer1, Feng He, Theodore G Wensel

  • 1Department of Ophthalmology, Baylor College of Medicine, Houston, Texas 77030, USA.

Abstract

Insights

Intravitreal moxifloxacin demonstrated rapid clearance in rabbit eyes with a half-life of 1.72 hours. Therapeutic levels were maintained for 12 hours, suggesting potential for treating bacterial endophthalmitis.

Area of Science:

  • Ophthalmology
  • Pharmacokinetics
  • Microbiology

Background:

  • Bacterial endophthalmitis is a severe intraocular infection requiring prompt and effective treatment.
  • Intravitreal antibiotics are a common approach for managing endophthalmitis.
  • Moxifloxacin is a fluoroquinolone with broad-spectrum activity against common ocular pathogens.

Purpose of the Study:

  • To determine the vitreous clearance and pharmacokinetic profile of moxifloxacin following intravitreal injection in a rabbit model.
  • To assess the duration of therapeutic drug concentrations in the vitreous humor.

Main Methods:

  • Intravitreal injections of moxifloxacin (200 microg/0.1 mL) were administered to rabbit eyes.
  • Vitreous samples were collected at various time points post-injection (1, 6, 12, 24, 36, and 48 hours).
  • Moxifloxacin concentrations in vitreous humor were quantified using high-performance liquid chromatography (HPLC).

Main Results:

  • Moxifloxacin exhibited an exponential decay in vitreous concentration with a calculated half-life of 1.72 hours.
  • Mean vitreous concentrations were 120.49 microg/mL at 1 hour, decreasing to 20.23 microg/mL at 6 hours and 1.06 microg/mL at 12 hours.
  • Achieved concentrations significantly exceeded the MIC90 for common bacterial endophthalmitis pathogens.

Conclusions:

  • Intravitreal moxifloxacin maintained therapeutic concentrations in rabbit vitreous for at least 12 hours post-injection.
  • The pharmacokinetic profile supports the potential utility of intravitreal moxifloxacin in the treatment of bacterial endophthalmitis.
  • Further clinical studies are warranted to confirm efficacy and safety in human patients.

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