A simple corneal perfusion chamber for drug penetration and toxicity studies
- aDepartment of Ophthalmology, Flinders University of South Australia, Adelaide, Australia, bMoorfields Eye Hospital, London, UK, cBiomedical Engineering, Flinders Medical Centre, Adelaide, Australia, dDepartment of Ophthalmology, Emory University, Atlanta, USA
- Dr K A Williams, Department of Ophthalmology, Flinders University of South Australia, GPO Box 2100, Adelaide, SA 5001, Australiakeryn.williams{at}flinders.edu.au
- Accepted 13 September 2000
Abstract
AIMS Corneal perfusion chambers are important tools in the development and assessment of ophthalmic drugs. The aim of this study was to design and test a modified perfusion chamber suitable for topical application of drugs to isolated corneoscleral preparations, and which allowed continuous monitoring of endothelial cell function.
METHODS A polycarbonate and stainless steel perfusion chamber was designed to clamp corneas in a horizontal plane suitable for topical drug delivery. Endothelial cell function was assessed by ultrasonic pachymetry and specular microscopy during perfusion. Epithelial barrier function was assessed by penetration of fluorescein. Leakage was examined by measuring penetration of a large protein, IgG. Tissue architecture after perfusion was examined by conventional histology.
RESULTS Corneas maintained a functionally and morphologically intact endothelial monolayer during perfusion periods of up to 14 hours. The epithelial barrier function was well preserved. The tissue clamp sealed the preparation effectively against leakage of macromolecules.
CONCLUSION The new chamber device forms a reliable tool for in vitro drug penetration and toxicity studies in isolated perfused corneoscleral tissue.
