Publication:
Artemether Bioavailability after Oral or Intramuscular Administration in Uncomplicated Falciparum Malaria

dc.contributor.authorKamolrat Silamuten_US
dc.contributor.authorPaul N. Newtonen_US
dc.contributor.authorPaktiya Teja-Isavadharmen_US
dc.contributor.authorYupin Suputtamongkolen_US
dc.contributor.authorDuangsuda Siriyanondaen_US
dc.contributor.authorManeerat Rasameesorajen_US
dc.contributor.authorSasithon Pukrittayakameeen_US
dc.contributor.authorNicholas J. Whiteen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherArmed Forces Research Institute of Medical Sciences, Thailanden_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherJohn Radcliffe Hospitalen_US
dc.date.accessioned2018-07-24T03:28:35Z
dc.date.available2018-07-24T03:28:35Z
dc.date.issued2003-12-01en_US
dc.description.abstractThe antimalarial activity of artemether following oral or intramuscular administration in the plasma of 15 adults with acute uncomplicated Plasmodium falciparum malaria was measured by bioassay. The peak concentrations in plasma following oral administration were higher in patients with acute illness (median, 1,905 mmol of dihydroartemisinin [DHA] equivalents per liter; range, 955 to 3,358 mmol of DHA equivalents per liter) than in patients in the convalescent phase (median, 955 mmol of DHA equivalents per liter; range, 576 to 1,363 mmol of DHA equivalents per liter), and clearance (CL/F) was lower in patients in the acute phase (1.11 liters/kg/h; range, 0.21 to 3.08 liters/kg/h) than in patients in the convalescent phase (median, 2.76 liters/kg/h; range, 1.56 to 5.74 liters/kg/h) (P ≤ 0.008). Antimalarial activity in terms of the peak concentration in plasma (Cmax) after oral administration was a median of 16 times higher than that after intramuscular administration. The ratio of the area under the plasma concentration-time curve during the first 24 h (AUC0-24) after oral administration of artemether to the AUC0-24after intramuscular administration was a median of 3.3 (range, 1 to 11) (P = 0.0001). In the acute phase, the time to Cmaxwas significantly shorter after oral administration (median, 1 h; range, 0.5 to 3.0 h) than after intramuscular administration (median, 8 h; range, 4 to 24 h) (P = 0.001). Intramuscular artemether is absorbed very slowly in patients with acute malaria.en_US
dc.identifier.citationAntimicrobial Agents and Chemotherapy. Vol.47, No.12 (2003), 3795-3798en_US
dc.identifier.doi10.1128/AAC.47.12.3795-3798.2003en_US
dc.identifier.issn00664804en_US
dc.identifier.other2-s2.0-0344012029en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/21006
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0344012029&origin=inwarden_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleArtemether Bioavailability after Oral or Intramuscular Administration in Uncomplicated Falciparum Malariaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0344012029&origin=inwarden_US

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