J.M.Nguta a *, J.M.Mbaria a , D.W.Gakuya a , P.K.Gathumbi a , J.D.Kabasa b , S.G.Kiama a
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Transcript of J.M.Nguta a *, J.M.Mbaria a , D.W.Gakuya a , P.K.Gathumbi a , J.D.Kabasa b , S.G.Kiama a
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J.M.Ngutaa*, J.M.Mbariaa, D.W.Gakuyaa, P.K.Gathumbia, J.D.Kabasab, S.G.Kiamaa
aUniversity of Nairobi, Nairobi, Kenya bMakerere University, Kampala, Uganda
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Malaria is the single most cause of ill health, death and poverty in sub-saharan Africa
There are as many as 300 m acute cases of malaria worldwide each year, resulting in 1m deaths
90% of these deaths occur in sub-saharan Africa, and majority of victims are children aged less than 5 yrs
Malaria is a major obstacle to social economic growth in Africa, accounting for 40% of public health expenditure
Nguta et al, 2010. Journal of Ethno pharmacology
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In Kenya, 22M people are at risk, 70% of them are in rural areas
About 34,000 Kenyan children die every year from malaria compared to a total estimate of 42,000 people dead
80% of people worldwide are estimated to use herbal remedies against common diseases including malaria.
However, few data are available on their safety.
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The current study was designed to evaluate the acute toxicity of crude plant extracts used against malaria in Kenya in Artemia salina larvae
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Study site (Msambweni district)
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Preparation of extracts Aqueous Organic (CHCL3/MeOH, 1:1) –Cold
maceration
Acute toxicity determination The procedure of Meyer et al (1982), was
adopted for LC50 determination
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Only 24% of the aqueous crude extracts used against malaria in Msambweni, Kenya are safe
Only 4.5% of organic extracts screened were found be safe in brine shrimp lethality assay
Majority of crude extracts could not make safe antimalarials
Further antimalarial and phytochemical work is underway
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Carnegie Corporation of New York through RISE-AFNNET (for funding)
RISE-AFNNET colleagues ICOPHAI 2011 organizing committee for a
travel grant and invitation University of Nairobi (Granting paid leave) ICOPHAI 2011 Participants (For their
attention). AHSANTENI SANA!