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. 2012 Jun;56(6):3288–3297. doi: 10.1128/AAC.06232-11

Table 4.

Final population pharmacokinetic estimates and bootstrap results for artemisinin (n = 12)a

Parameter Mean (RSE %) Bootstrap median [95% CI]
Structural model parameters
    ka (per h) 1.67 (55) 1.62 [1.01–4.40]
    CL/FART (liter/h/70 kg) 124 (12) 125 [99–157]
    VC/FART (liter/70 kg) 590 (30) 533 [318–874]
    Q/FART (liter/h/70 kg) 43.7 (38) 46.4 [19.5–79.4]
    VP/FART (liter/70 kg) 435 (26) 456 [259–696]
F2,ART − relative bioavailability of 2nd dose 0.270 (17) 0.275 [0.192–0.368]
Random model parameters
    IOV in FART (%) 43 (27) 39 [15–58]
    IIV in CL/FART (%) 12 (29) 12 [4–18]
    Residual variability (%) 33 (11) 32 [26–38]
a

Parameters are ka (absorption rate constant), CL/FART (clearance), VC/FART (central volume of distribution), VP/FART (peripheral volume of distribution), Q/FART (intercompartmental clearance between VP/FART and VC/FART), and F2,ART (relative bioavailability of 2nd dose of ART). RSE (relative standard error) values were calculated from bootstrap results. OFV in final model, −63.562; bootstrap OFV (median [95% CI], −73.838 [−110.720 to 43.043].