Results 111 to 120 of about 8,298 (167)

Antimalarial cabamiquine inhibits blood-stage of different field isolates of Plasmodium species. [PDF]

open access: yesBMC Infect Dis
Dembele L   +10 more
europepmc   +1 more source

First TES in Djibouti: A Critical Milestone Amid Rising Regional Threats. [PDF]

open access: yesOpen Forum Infect Dis
Behaksra SW   +25 more
europepmc   +1 more source

Genotype Complexity Modulates Antimalarial Susceptibility in vitro. [PDF]

open access: yesInfect Drug Resist
Egwu CO   +7 more
europepmc   +1 more source

<i>Plasmodium falciparum</i> field isolates drug susceptibility in Mali. [PDF]

open access: yesJAC Antimicrob Resist
Maiga FO   +11 more
europepmc   +1 more source

Defining safety parameters for first-trimester malaria treatment trials: stakeholder views from Real-Time Delphi survey. [PDF]

open access: yesMalar J
Bivegete S   +10 more
europepmc   +1 more source

A Controlled Human Malaria Infection model for relapsing Plasmodium vivax

open access: yes
Duncan AD   +39 more
europepmc   +1 more source

Genomic Surveillance of malaria reveals localized sporadic emergence of artemisinin partial resistance and wide-spread sulfadoxine-pyrimethamine resistance in Ghana

open access: yes
Dorvi IN   +24 more
europepmc   +1 more source

Gender Differences in Pharmacokinetics of Lumefantrine and Its Metabolite Desbutyl-Lumefantrine in Rats

Biopharmaceutics and Drug Disposition, 2012
ABSTRACTLumefantrine has been reported to be mainly bio‐transformed by cytochrome P450 isozyme 3A4 to desbutyl‐lumefantrine (DLF) in human liver microsomes. Since CYP3A is expressed in a sex specific manner in rats, it could be expected that the pharmacokinetics of lumefantrine would be changed in male rats compared with those in female rats.
Sheelendra Pratap Singh   +1 more
exaly   +3 more sources

Enantioselective in vitro ADME, absolute oral bioavailability, and pharmacokinetics of (−)-lumefantrine and (+)-lumefantrine in mice

Xenobiotica, 2020
Lumefantrine (LFN) is a chiral antimalarial drug. Enantioselective in vitro attributes and absolute oral pharmacokinetics for (-)-LFN and (+)-LFN have been characterized in mice. No stereoselectivity was seen with either of the enantiomers when compared with rac-LFN in the executed in vitro studies (solubility, metabolic stability, protein binding ...
Bhavesh Babulal Gabani   +6 more
openaire   +2 more sources

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