Publications by authors named "Fatoumata O Maiga"

Article Synopsis
  • The study investigates the effects of cabamiquine and pyronaridine on the P. falciparum malaria parasite, looking at their performance as standalone treatments and in combination therapy.
  • Using field isolates and a pharmacometrics model, researchers create an interaction map to simulate effective clinical dose ratios for these antimalarials.
  • Results indicate that while pyronaridine alone is less effective, the combination of cabamiquine and pyronaridine significantly improves parasite killing, suggesting the methodology can aid in developing new malaria treatments.
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Imidazolopiperazine (IPZ), KAF156, a close analogue of GNF179, is a promising antimalarial candidate. IPZ is effective against and clinical malaria in human with transmission blocking property in animal models and effective against liver stage parasites. Despite these excellent drug efficacy properties, in vitro parasites have shown resistance to IPZ.

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Structural biology is an essential tool for understanding the molecular basis of diseases, which can guide the rational design of new drugs, vaccines, and the optimisation of existing medicines. However, most African countries do not conduct structural biology research due to limited resources, lack of trained persons, and an exodus of skilled scientists. The most urgent requirement is to build on the emerging centres in Africa - some well-established, others growing.

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Background: Artemisinin-based combination therapy (ACT) was deployed in 2005 as an alternative to chloroquine and is considered the most efficacious treatment currently available for uncomplicated falciparum malaria. While widespread artemisinin resistance has not been reported to date in Africa, recent studies have reported partial resistance in Rwanda. The purpose of this study is to provide a current systematic review and meta-analysis on ACT at Mali study sites, where falciparum malaria is highly endemic.

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