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2007 OMIG, Abstract 12

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The Ocular Distribution and Kinetics of Moxifloxacin Following Prophylactic Dosing Regimens and an Intracameral Injection in Rabbits.
G.R. Owen, L.F. Bernal-Perez, A.C. Brooks
Alcon Research, Ltd., Fort Worth, TX

Purpose: To determine the concentration of moxifloxacin in ocular tissues following two prophylactic topical dosing regimens, and after an intracameral injection in a rabbit model that mimics the human eye.
Methods: Rabbits were dosed topically with moxifloxacin 0.5% (Vigamox ®) by two different regimens: A) four doses every 15 minutes for one hour prior to collection, or B) a single dose one hour before collection.  The rabbit model that was used mimicked the human eye by manual blinking at the rate of 4 blinks/min and adding supplementary tears at the rate of 2 μL/min.  The third group of rabbits (C) were given an intracameral injection of moxifloxacin 0.5% (50 μL) into the aqueous humor.
The concentration of moxifloxacin (μg/mL or μg/g) was determined by HPLC.
Results:                             


Regimen

A

B

C

Time

At Collection

Initial

4 Hrs

6 Hrs

12 Hrs

Aqueous Humor

  7

1.4

710

  6.0

0.5

0.2

Cornea

32

6.9

-

17.2

1.3

0.4

Conjunctiva

  8

0.4

-

  0.4

<0.05

<0.05

Iris-Ciliary Body

  6

0.9

-

  2.7

0.3

0.2

Conclusions: The moxifloxacin MIC for a typical fluoroquinolone resistant isolate of Staphylococcus aureus and S. epidermidis is 2.0 μg/mL (Surv. Ophthal. 2005; 50:S16-31). Topical dosing by regimen A resulted in an aqueous humor concentration more than 3x this MIC at the time of collection.  This is more than 100x the MIC (0.05 μg/mL) of fluoroquinolone sensitive staphylococci.  An intracameral injection of Vigamox ® (C) maintained this same concentration (6-7 μg/mL) through 4 hours post surgery.

Disclosure code:  E

 

 

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