Efficacy of trypan ®: a diminazene based drug as antileishmanial agent

Trypan ®, a diamidine based drug, was tested as an antileishmanial agent. Duplicate cultures of both Leishmania major and Leishmania donovani promastigotes in M199 medium and Trypan ® at various concentrations were tested. The cultures were incubated at 25 °C and parasites counted at 48 h interval,...

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Bibliographic Details
Published inActa tropica Vol. 92; no. 3; pp. 267 - 272
Main Authors Macharia, J.C., Bourdichon, A.J., Gicheru, M.M.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.11.2004
Elsevier
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Summary:Trypan ®, a diamidine based drug, was tested as an antileishmanial agent. Duplicate cultures of both Leishmania major and Leishmania donovani promastigotes in M199 medium and Trypan ® at various concentrations were tested. The cultures were incubated at 25 °C and parasites counted at 48 h interval, and the data generated was used to establish growth inhibition curves. Drug-free cultures were included to serve as control. In the in vivo study, a total of 40 BALB/c mice were divided into five groups of 8 mice each. They were infected with 2 × 10 6 promastogotes on the left footpad. Two groups were treated with 70 μg/ml of Trypan ®, a total of 500 μl used immediately after infection, one group by topical application and the other administered intraperitoneally. The treatments were repeated for the two other groups 10 weeks post infection, one by topical application and the other administered intraperitoneally. One group was not treated and thus served as control. Footpad sizes were measured using Vernier calliper every 2 weeks for 21 weeks. In the in vitro studies, Trypan ® inhibited growth of either L. major or L. donovani promastigotes in all the concentrations tested with more dramatic inhibition in high concentrations. Based on the in vivo studies, it was evident that Trypan ® had effect on L. major infected lesions when applied topically immediately after infection. However, there was no effect when treatment commenced after the lesions were established. The data is discussed.
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ISSN:0001-706X
1873-6254
DOI:10.1016/j.actatropica.2004.08.008