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. 2011 Dec;39(12):2182–2190. doi: 10.1124/dmd.111.040212

TABLE 5.

Steady-state pharmacokinetics of silybin A conjugates and silybin B conjugates

Results are shown as geometric means (95% confidence interval), except for Tmax, which is shown as median (minimum, maximum). Data are for n = 6 subjects, except for the HCV 560-mg steady-state cohort where n = 5; one subject was dropped from the pharmacokinetic analysis because of incorrect dosing for pharmacokinetic sampling at steady state on day 8.

Cohort PK Parameter SAconjugates
SBconjugates
HCV NAFLD HCV NAFLD
280 mg AUC0–8 h (ng · h/ml) 2048 (1465–2815) 1297 (652–2271) 7278 (5633–9287)* 3962 (2338–6292)
Cmax (ng/ml) 369 (294–459)* 233 (146–352) 1294 (1040–1589)* 750 (563–981)
Tmax (h) 2 (1, 4) 2 (0, 4) 2 (1, 4) 1.8 (0, 2)
t1/2 (h) 5 (3–8.3) 6.8 (2.5–15.5) 4.3 (2.8–6.3) 5.1 (1.2–12.7)
560 mg AUC0–8 h (ng · h/ml) 3229 (1618–5348) 2902 (1403–5163) 11003 (3244–21,930) 7745 (4312–12,547)
Cmax (ng/ml) 543 (182–1050) 529 (287–894) 2074 (700–4103) 1592 (927–2600)
Tmax (h) 2 (0, 4) 4 (0, 6) 2 (2, 4) 3 (0, 4)
t1/2 (h) 6.2 (3.6–9.3) 3.6 (2.7–4.7) 4.1 (2.9–5.6) 2.8 (1.9–3.9)

SA, silymarin A; SB, silymarin B.

*

p < 0.05.