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In vivo activity of perifosine against Leishmania amazonensis.

Abstract
Miltefosine has been established as the first oral administration drug against cutaneous and visceral leishmaniasis. Other alkyl-phospholipids such as edelfosine have been tested against Leishmania showing an in vitro antiparasitic activity. Perifosine in vitro activity has been previously demonstrated against different Leishmania species including Leishmania amazonensis. In this study edelfosine and perifosine were orally administered to BALB/c mice at doses of 1 and 2.5 mg/kg/day during 28 days and 5 mg/kg/day during 14 days, starting the treatment 2 weeks after the first treatment scheme. Lesion sizes and parasitic burden as well as viability were determined in order to establish the treatment effectiveness. An assay to compare miltefosine at standard dose of 2.5 mg/kg/day during 28 days to an in vivo treatment with perifosine at the most effective treatment scheme observed in this study 5 mg/kg/day during 14 days, was also developed. Perifosine showed the higher activity in the in vivo assay and is showing as a new possibility within the alkyl-phospholipids group for the treatment against cutaneous leishmaniasis caused by L. amazonensis.
AuthorsM Gabriela Cabrera-Serra, Basilio Valladares, Jose E Piñero
JournalActa tropica (Acta Trop) Vol. 108 Issue 1 Pg. 20-5 (Oct 2008) ISSN: 1873-6254 [Electronic] Netherlands
PMID18801328 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antiprotozoal Agents
  • Phospholipid Ethers
  • Phosphorylcholine
  • edelfosine
  • perifosine
  • miltefosine
Topics
  • Administration, Oral
  • Animals
  • Antiprotozoal Agents (administration & dosage, therapeutic use)
  • Female
  • Leishmania mexicana (drug effects, isolation & purification)
  • Leishmaniasis, Cutaneous (drug therapy, parasitology, pathology)
  • Mice
  • Mice, Inbred BALB C
  • Phospholipid Ethers (administration & dosage, therapeutic use)
  • Phosphorylcholine (administration & dosage, analogs & derivatives, therapeutic use)
  • Survival Analysis

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