TY - JOUR
T1 - Drug cytotoxicity assay for african trypanosomes and leishmania species
AU - Bodley, Annette L.
AU - Mc Garry, Michael W.
AU - Shapiro, Theresa A.
N1 - Funding Information:
Grant support: National Institutes of Health (AI-28855), United Nations Development ProgrammelWORLD BANK/World Health Organization Special Program for Research and Training in Tropical Diseases, and Burroughs Wellcome Fund Experimental Therapeutics Award (to T.A.S.).
PY - 1995/10
Y1 - 1995/10
N2 - The trypanosomes and Leishmania species are parasitic protozoa that afflict millions of people throughout the world. If not treated, African trypanosomiasis and visceral leishmaniasis are fatal. The available drugs are severely limited by toxicity, marginal efficacy, the requirement for parenteral administration, and spreading drug resistance. In this study, a spectrophotometric assay was developed and validated for measuring the cytotoxicity of test compounds against axenically cultured bloodstream-form Trypanosoma brucei (African trypanosomes) and promastigotes of Leishmania donovani. Enzymatic hydrolysis of p-nitrophenyl phosphate, monitored by a microtiter plate reader, is a reliable surrogate for parasite cell counts. The assay is simple, inexpensive, and highly reproducible. The coefficient of variation for EC50values is <10% for determinations obtained over several months. This method permits the rapid screening of candidates for much-needed new drugs against these parasites.
AB - The trypanosomes and Leishmania species are parasitic protozoa that afflict millions of people throughout the world. If not treated, African trypanosomiasis and visceral leishmaniasis are fatal. The available drugs are severely limited by toxicity, marginal efficacy, the requirement for parenteral administration, and spreading drug resistance. In this study, a spectrophotometric assay was developed and validated for measuring the cytotoxicity of test compounds against axenically cultured bloodstream-form Trypanosoma brucei (African trypanosomes) and promastigotes of Leishmania donovani. Enzymatic hydrolysis of p-nitrophenyl phosphate, monitored by a microtiter plate reader, is a reliable surrogate for parasite cell counts. The assay is simple, inexpensive, and highly reproducible. The coefficient of variation for EC50values is <10% for determinations obtained over several months. This method permits the rapid screening of candidates for much-needed new drugs against these parasites.
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U2 - 10.1093/infdis/172.4.1157
DO - 10.1093/infdis/172.4.1157
M3 - Article
C2 - 7561203
AN - SCOPUS:0029128640
SN - 0022-1899
VL - 172
SP - 1157
EP - 1159
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 4
ER -