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Updated: Aug 20, 2026

Ex Vivo and In Vivo Animal Models for Mechanical and Chemical Injuries of Corneal Epithelium
Published on: April 6, 2022
Diffusion of metronidazole released from aqueous solution and a gel through human and rabbit corneas
Pieter van der Bijl1, Armorél D van Eyk, Heiner I Seifart
1Department of Pharmacology, Faculty of Health Sciences, University of Stellenbosch, Tygerberg, South Africa. pvdb@sun.ac.za
Abstract:
Metronidazole has been suggested as an adjunct in the treatment of Acanthamoeba keratitis. This study involves the permeation of metronidazole from topically applied solutions and gels through human and rabbit corneas. The permeation of metronidazole, from the solutions and gels through the corneas, was determined using a flow-through diffusion apparatus. Human (32) and rabbit (54) corneas were obtained from an eye bank and animal nursery farm, respectively. Experiments were conducted at 20 degrees C and over a time period of 24 hours. High-performance liquid chromatography (HPLC) analysis was used as a detection method. Statistical tests used included an Analysis of Variance (ANOVA) and Duncan's multiple range test, for a determination of the steady state, and a nonlinear regression analysis, using an F test, was used to compare entire curves. Flux rates for 0.5% and 1% metronidazole solutions across human corneas were found to be 14% and 30% higher, respectively, than for rabbit corneas. However, the flux rates of the 0.5% and 0.8% metronidazole gels across rabbit corneas were found to be 7% and 25% higher than those for human corneas. The flux rates measured for at least the first 10 hours were not, statistically, significantly different between the metronidazole released from aqueous solutions and from the gel. Steady-state flux rates of the 0.5% metronidazole aqueous and gel formulations were approximately half those of the 0.8% and 1% preparations. Because of the longer corneal contact times, it may be therapeutically advantageous to use 0.8% metronidazole concentrations in gels for treating Acanthamoeba keratitis infestations. Further in vivo studies on the ocular compatibility of these formulations need to be performed. The use of rabbit corneas as an in vitro permeability model for human corneas is supported by these studies.
Insights
Metronidazole gel formulations, particularly at 0.8% concentration, show therapeutic promise for Acanthamoeba keratitis due to enhanced corneal permeation and contact time compared to solutions. Rabbit corneas serve as a reliable in vitro model for human corneal permeability studies.
Area of Science:
- Ophthalmology
- Pharmacology
- Biomaterials
Background:
- Acanthamoeba keratitis (AK) is a severe microbial infection of the cornea.
- Metronidazole is a potential adjunctive treatment for AK.
- Understanding drug permeation through the cornea is crucial for effective topical therapy.
Purpose of the Study:
- To investigate the corneal permeation of metronidazole from topical solutions and gels.
- To compare the permeability of metronidazole through human and rabbit corneas.
- To evaluate the potential therapeutic advantage of metronidazole gel formulations for AK treatment.
Main Methods:
- Human and rabbit corneas were used in a flow-through diffusion apparatus.
- Metronidazole permeation was studied from solutions and gels at various concentrations (0.5%–1%).
- High-performance liquid chromatography (HPLC) was used for detection; statistical analyses included ANOVA and nonlinear regression.
Main Results:
- Metronidazole solutions showed higher flux rates in human corneas than rabbit corneas at 0.5% and 1%.
- Metronidazole gels exhibited higher flux rates in rabbit corneas than human corneas at 0.5% and 0.8%.
- No significant difference in flux rates between solutions and gels within the first 10 hours; higher concentrations (0.8%, 1%) demonstrated greater steady-state flux.
Conclusions:
- 0.8% metronidazole gel formulations may offer therapeutic advantages for Acanthamoeba keratitis due to increased corneal contact time.
- Rabbit corneas are a suitable in vitro model for predicting human corneal permeability of metronidazole.
- Further in vivo studies are required to assess the ocular compatibility of these metronidazole formulations.
