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Enantiospecific Reassessment of the Pharmacokinetics and Pharmacodynamics of Oral Eflornithine against Late-Stage Trypanosoma brucei gambiense Sleeping Sickness

Artikel i vetenskaplig tidskrift
Författare Rasmus Jansson Löfmark
K. Na-Bangchang
S. Bjorkman
F. Doua
Michael Ashton
Publicerad i Antimicrobial Agents and Chemotherapy
Volym 59
Nummer/häfte 2
Sidor 1299-1307
ISSN 0066-4804
Publiceringsår 2015
Publicerad vid Institutionen för neurovetenskap och fysiologi, sektionen för farmakologi
Sidor 1299-1307
Språk en
Länkar dx.doi.org/10.1128/aac.04101-14
Ämnesord HUMAN AFRICAN TRYPANOSOMIASIS, CEREBROSPINAL-FLUID, ALPHA-DIFLUOROMETHYLORNITHINE, ORNITHINE-DECARBOXYLASE, COMBINATION, THERAPY, DRUG ABSORPTION, MODEL, MELARSOPROL, ENANTIOMERS, PLASMA, Microbiology, Pharmacology & Pharmacy
Ämneskategorier Farmakologi

Sammanfattning

This study aimed to characterize the stereoselective pharmacokinetics of oral eflornithine in 25 patients with late-stage Trypanosoma brucei gambiense sleeping sickness. A secondary aim was to determine the concentrations of L-and D-eflornithine required in plasma or cerebrospinal fluid (CSF) for an efficient eradication of the T. brucei gambiense parasites. Patients were randomly allocated to receive either 100 (group I, n = 12) or 125 (group II, n = 13) mg/kg of body weight of drug every 6 h for 14 days. The concentrations of L-and D-eflornithine in the plasma and CSF samples were measured using a stereospecific liquid chromatographic method. Nonlinear mixed-effects modeling was used to characterize the plasma pharmacokinetics. The plasma concentrations of L-eflornithine were on average 52% (95% confidence interval [CI], 51, 54%; n = 321) of the D-enantiomer concentrations. The typical oral clearances of L-and D-eflornithine were 17.4 (95% CI, 15.5, 19.3) and 8.23 (95% CI, 7.36, 9.10) liters/h, respectively. These differences were likely due to stereoselective intestinal absorption. The distributions of eflornithine enantiomers to the CSF were not stereoselective. A correlation was found between the probability of cure and plasma drug exposure, although it was not more pronounced for the L-enantiomer than for that of total eflornithine. This study may explain why oral treatment for late-stage human African trypanosomiasis (HAT) patients with racemic eflornithine has previously failed; the more potent L-enantiomer is present at much lower concentrations in both plasma and CSF than those of the D-enantiomer. Eflornithine stereoselective pharmacokinetics needs to be considered if an oral dosage regimen is to be explored further.

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