Amoebicidal activities of Alexidine against 3 pathogenic strains of Acanthamoeba

Hassan Alizadeh, Sudha Neelam, Harrison D Cavanagh

Research output: Contribution to journalArticlepeer-review

19 Scopus citations


OBJECTIVES: Effective pharmacotherapy for Acanthamoeba keratitis has been hampered because of the marked resistance of various stains to a variety of antimicrobial agents. In view of the fact that topical Brolene (propamidine isethionate) and neosporin are currently considered to be the first-line medical treatment of choice in Europe, we sought to determine whether Alexidine is equally effective, because the latter drug is more readily available in the United States. METHODS: Trophozoites and cysts from 3 pathogenic corneal isolates (A. castellanii, A. polyphaga, and A. rhysodes) were incubated in peptone-yeast extract-glucose medium containing different concentrations of Alexidine for 24 hr. The number of trophozoites was counted by hemocytometer. The cysts were plated in to nonnutrient agar plates precoated with Escherichia coli and observed for viability or excystment over a period of 2 weeks. The capacity of different concentrations of Alexidine to induce cytolysis of corneal epithelial cells was tested in vitro. Chinese hamster corneas were treated with 5 μL of Alexidine topically, every hour; 6 times a day and the corneas were stained with fluorescein to asses the epithelial defects in vivo. RESULTS: Alexidine was effective in killing the trophozoites at a concentration of 10 μg/mL. However, a higher concentration of Alexidine (100 μg/mL) is required to kill Acanthamoeba cysts and the cytotoxic activities of Alexidine are comparable with chlorhexidine. We have also demonstrated that both Alexidine and chlorhexidine at 100 μg/mL induced significant cytopathic effect on the corneal epithelial cells in vitro. In vivo results indicate that Alexidine at a concentration of 100 μg/mL is less toxic than chlorhexidine when applied topically to the Chinese hamster cornea. CONCLUSIONS: Our study has identified Alexidine as a novel anti-Acanthamoeba drug and suggests that Alexidine may be an effective therapeutic option because of its potency and low toxicity to the corneal tissues when applied topically in vivo.

Original languageEnglish (US)
Pages (from-to)1-5
Number of pages5
JournalEye and Contact Lens
Issue number1
StatePublished - Jan 2009


  • Acanthamoeba
  • Alexidine
  • Corneal epithelial cells
  • Cytolysis
  • Cytotoxicity

ASJC Scopus subject areas

  • Ophthalmology


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