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Assessment of drugs against Cryptosporidium parvum using a simple in vitro screening method
Journal article   Peer reviewed

Assessment of drugs against Cryptosporidium parvum using a simple in vitro screening method

A. Armson, B.P. Meloni, J.A. Reynoldson and R.C.A. Thompson
FEMS Microbiology Letters, Vol.178(2), pp.227-233
1999
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Abstract

A rapid semi-quantitative screening method was devised for assessing the anticryptosporidial and cytotoxic effects of putative chemotherapeutic compounds. The method is suitable as an initial rapid screening procedure from which compounds demonstrating anticryptosporidial activity can be identified for further analysis. It has the advantages of speed, low cost and concurrent assessment of anticryptosporidial and cytotoxic effects and allows accurate determination of minimum lethal concentrations. Of the 71 compounds screened, six completely inhibited cryptosporidial growth at 1 μM (monensin, salinomycin, alborixin, lasalocid, trifluralin and nicarbazin) and a further eight showed significant anticryptosporidial activity at 1 or 20 μM (halquinol, bleomycin, suramin, mitomycin, doxycycline hydrochloride, toltrazuril, chloroquine phosphate and teniposide). Twelve compounds were found to have some degree of cytotoxicity at 1 μM and a further 12 at 20 μM. Copyright (C) 1999 Federation of European Microbiological Societies.

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Citation topics
1 Clinical & Life Sciences
1.246 Diarrheal Diseases
1.246.985 Cryptosporidium
Web Of Science research areas
Microbiology
ESI research areas
Microbiology
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