Skip to main content
. 2009 Aug 26;90(4):1029–1037. doi: 10.3945/ajcn.2009.27981

TABLE 1.

Comparison of the plasma pharmacokinetics determined after a single-bolus, 20-mg dose of S-(−)[2-13C]equol, R-(+)[2-13C]equol, and (±)[2-13C]equol in the same 12 healthy adults1

R-(+)[2-13C]equol S-(−)[2-13C]equol (±)[2-13C]equol
tmax (h) 2.92 ± 0.66 3.17 ± 0.63 5.75 ± 0.87
Cmax (nmol/L · h) 1202 ± 1482 991 ± 1292 567 ± 66
AUCinf (nmol/L · h) 12,230 ± 7702 11,048 ± 1276 9047 ± 1001
Vz/F (L) 71.3 ± 8.2 96.2 ± 12.4 132 ± 23.8
t1/2 (h) 6.90 ± 0.52 7.89 ± 0.69 8.15 ± 0.53
Cl/F (L/h) 7.08 ± 0.423 8.73 ± 1.23 10.73 ± 1.44
1

All values are means ± SEMs. tmax, time to reach maximum concentration; Cmax, maximum plasma concentration; AUCinf, total area under the plasma concentration-time curve; Vz/F, apparent volume of distribution; t1/2, terminal elimination half-life; Cl/F, systemic clearance. Repeated-measures ANOVA were calculated for each test, and matched-pairs t tests were conducted with Bonferroni correction for multiple comparisons.

2

Significantly different from (±)[2-13C]equol, P < 0.05.

3

Significantly different from S-(−)[2-13C]equol and (±)[2-13C]equol, P < 0.05.