Toxicity of antiglaucoma drugs with and without benzalkonium chloride to cultured human corneal endothelial cells

• Published in: Clinical ophthalmology (Auckland, N.Z.) Vol. 4; no. default; pp. 1217 - 1222
• Main Authors: Ayaki, Masahiko, Iwasawa, Atsuo, Inoue, Yoichi
• Format: Journal Article
• Language: English
• Published: New Zealand Taylor & Francis Ltd 21.10.2010; Dove Press; Dove Medical Press
• Subjects: cell viability score; Chemical vapor synthesis; Culture; Dilution; Drugs; Endothelial cells; eye drop; Maleates; Ophthalmology; Original Research; preservatives; Toxicity; Viability; cell viability score; preservatives; eye drop
• ISSN: 1177-5483; 1177-5467; 1177-5483
• DOI: 10.2147/OPTH.S13708

The toxicity of antiglaucoma medications to ocular surface cells has been evaluated extensively; however, the toxicity to corneal endothelial cells (CECs) remains elusive. Our aim is to evaluate the toxicity of antiglaucoma medications to CECs using an in vitro toxicity assay. Primary cultures of human (H) CECs derived from eye bank specimens were established. Following exposure of HCECs to test solutions for 10, 30, or 60 minutes, or 48 hours, we measured cell viability using a WST-1 assay. Test solutions were diluted in culture media and included 0.5% Timoptol(®), preservative-free 0.5% timolol maleate, 1% Trusopt(®), preservative-free 1% dorzolamide, Travatan(®), Travatan Z(®), Xalatan(®), and benzalkonium chloride (BAK). To assess cell viability, the value of the test culture well after treatment was expressed as a percentage of that of the control well. Toxicity of each solution was compared using the cell viability score (CVS). After exposure to 10-fold dilutions of test solutions for 48 hours, HCEC viabilities were 48.5% for 0.5% Timoptol, 80.9% for preservative-free 0.5% timolol maleate, 47.0% for 1% Trusopt, 71.7% for preservative-free 1% dorzolamide, 55.5% for Travatan, 88.5% for Travatan Z, and 52.5% for Xalatan. Exposure to test solutions diluted 100-fold or more resulted in HCEC viabilities >80%, with the exception of preservative-free 1% dorzolamide, which resulted in a viability of 72.0% at a dilution of 100-fold. Based on CVS, the order of cell viability was Travatan Z ≥ preservative-free timolol maleate = preservative-free dorzolamide > 0.5% Timoptol = 1% Trusopt > Travatan ≥ Xalatan. Assessment of the combined effect of drug and BAK revealed that latanoprost reduced the toxicity of BAK. Antiglaucoma eye drops produced HCEC toxicity that appeared to depend on the presence of BAK. Because dilution of the antiglaucoma solutions resulted in markedly lower HCEC toxicity, HCEC damage due to antiglaucoma medication may occur only in rare cases. The CVS was useful for comparison of the toxicity of the drugs.