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. 2000 Apr;44(4):972–977. doi: 10.1128/aac.44.4.972-977.2000

TABLE 4.

Summary of results of HPLC assays for artesunate and DHAa

Variable Oral administration
Convalescent phase
Intravenous administration
Artesunateb DHAc Artesunate DHA Artesunate DHA
No. of patients 3 3 1 1 2 2
AUC0–24 (ng · h/ml) 210 (70–667) 1,334 (1,018–2,673) 317 829 1,056 (322–1789) 3,999 (2,360–5,637)
k01 (h−1) 10.50 (2.55–47.91) 9.47 (2.36–9.69) 0.618 11.95
k10 (h−1) 1.29 (1.05–1.97) 1.06 (1.02–1.46) 0.623 0.248 3.00 (0.96–5.05) 1.93 (1.02–2.84)
thalf (h) 0.54 (0.35–0.66) 0.65 (0.47–0.68) 1.11 2.79 0.43 (0.14–0.72) 0.46 (0.24–0.68)
Tlag (h) 0.19 (0.00–0.25) 0.22 (0.14–0.45) 0.27 0.25
Tmax (h) 0.50 (0.25–0.50) 0.75 (0.5–1.0) 3 1
Cmax (ng/ml)d 198 (61–510) 1,052 (817–2,853) 98 294
V (liters/kg) 7.1 (1.8–31.4) 1.49 (0.68–1.69) 8.75 7.75 3.23 (0.62–5.84) 0.50 (0.36–0.64)
CL (liters/kg/h) 9.51 (2.99–32.80) 1.50 (0.75–2.24) 6.32 2.41 4.38 (3.19–5.58) 0.84 (0.66–1.01)
a

Values are medians (ranges). Abbreviations are as defined in footnotes a of Tables 2 and 3

b

To convert artesunate in nanograms per milliliter to nanomoles per liter, multiply by 2.601. 

c

To convert DHA in nanograms per milliliter to nanomoles per liter, multiply by 3.517. 

d

Cmax is the observed value for the oral administration data sets and the extrapolated value for the intravenous administration data sets.