JAC Advance Access published online on April 25, 2003
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dkg259
© 2003 by The British Society for Antimicrobial Chemotherapy
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Brief report
1 Department of Microbiology & Immunology,
University of Leicester, Medical Sciences Building, P.O. Box 138, University
Road, Leicester LE1 9HN
* Corresponding author. E-mail: sk46{at}le.ac.uk.
Received 14 January 2003
; revised 14 March 2003
; accepted 18 March 2003
Objectives: Microbial keratitis accounts
for up to 30% of blindness in some less developed societies.
The development of a single broad-spectrum topical antimicrobial
effective against bacteria, fungi and Acanthamoeba would
have a major impact on reducing the morbidity and simplifying the
treatment of microbial keratitis. To this end, the activity of the
amidoamine myristamidopropyl dimethylamine (MAPD) was investigated
against common causes of microbial keratitis. Methods: Challenge test assays were used to
study the efficacy of 50 mg/L MAPD against Pseudomonas
aeruginosa, Staphylococcus aureus, Candida
albicans, Fusarium solani and Acanthamoeba
polyphaga. Results: MAPD gave a 3.7 log kill of P.
aeruginosa after 60 min, 5.4 log for S. aureus by
45 min and 5 log for C. albicans and F.
solani within 15 min. A. polyphaga cysts were
reduced by 4 log within 120 min. Conclusions: The findings of this study confirm
that MAPD is an effective Acanthamoeba cysticidal
agent and extend the observation to demonstrate that it also possesses
excellent antifungal and antibacterial activity. MAPD may represent
a broad-spectrum therapeutic antimicrobial for keratitis and surgical
prophylaxis and deserves further evaluation in these roles.
Keywords: Acanthamoeba, keratitis, amidoamine,
antibacterial, antifungal
Activity of the amidoamine myristamidopropyl dimethylamine
against keratitis pathogens
2 Department
of Ophthalmology, Moorfields Eye Hospital, City Road,
London EC1V 2PD, UK
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