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

TABLE 3.

Means and 95% CIs or medians and ranges for pharmacokinetic variables for acute- and convalescent-phase oral administrationa

Variable Acute phaseb Convalescent phaseb P value
No. of subjects 19 15
AIC 158 (148–168) 130 (118–142)
Tmax (h) 0.75 (0.50–4.00)c 1.00 (0.50–4.00)c NS
Cmax (ng/ml) 1,021 (775–1267) 546 (379–715) 0.013
Tlag (h) 0.30 (0.16–0.44) 0.36 (0.18–0.54) NS
t1/2 (h) 0.71 (0.55–0.87) 0.84 (0.49–1.09) NS
k01 (h−1) 1.86 (0.80–20.87)c 3.44 (0.60–29.52)c NS
k10 (/h−1) 1.13d (0.96–1.30) 1.08d (0.78–1.38) NS
V/f (liters/kg) 1.33d (1.02–1.64) 3.15d (2.02–4.28) 0.005
CL/f (liters/kg/h) 1.38d (1.03–1.73) 2.54d (2.10–2.98) 0.003
AUC0–24 (ng · h/ml) 1,738d (1,412–2,064) 886d (733–1,039) 0.0005
a

Bioassay results are in DHA equivalents. Abbreviations are the same as defined in footnote a of Table 2 and as follows: AIC, Akaike Information Criterion; Tmax, observed time to Cmax; Cmax, maximum observed concentration; Tlag, absorption lag time; k01, absorption rate constant; V/f, total apparent volume of distribution per kilogram of body weight; f, fraction of the oral drug that is absorbed; NS, not significant. Values are means (95% CIs) unless indicated otherwise. 

b

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

c

Values are medians (ranges). 

d

Significantly (P < 0.01) different from mean for acute-phase intravenous administration (Table 2). For oral and convalescent-phase volume of distribution data compared with the estimated steady-state volume of distribution data, P was not significant P > 0.02.