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. 2010 Jul;70(1):126–131. doi: 10.1111/j.1365-2125.2010.03661.x

Table 2.

Pharmacokinetic parameters (mean ± SD) of bupropion and 4-hydroxybupropion after oral administration of bupropion 150 mg with or without woohwangcheongsimwon suspension to healthy male volunteers

Bupropion alone(n = 14) + Woohwangcheongsimwon(n = 14) Geometric mean ratios (90% CI) P value
Bupropion
AUC(0,∞) (ng ml−1 h) 991.0 ± 218.6 967.3 ± 219.0 0.976 (0.917, 1.04)
t1/2 (h) 17.9 ± 4.70 16.9 ± 4.75 0.935 (0.864, 1.01)
CL/F (l h−1) 164 ± 56.7 167 ± 57.8 1.02 (0.950, 1.09)
Cmax (ng ml−1) 105 ± 26.4 101 ± 34.5 0.948 (0.830, 1.08)
tmax (h) 3 (1–5)* 3 (1–5)* NS
CLR (l h−1) 0.374 ± 0.210 0.436 ± 0.285 1.13 (0.823, 1.56)
4-hydroxybupropion
AUC(0,∞) (ng ml−1 h) 15123 ± 4060.2 12922 ± 3542.4 0.856 (0.802, 0.912)
t1/2 (h) 20.9 ± 3.57 20.9 ± 3.84 0.999 (0.960, 1.04)
Cmax (ng ml−1) 405 ± 84.6 344 ± 84.2 0.845 (0.782, 0.914)
tmax (h) 6 (4–12)* 7 (5–12)* NS
Ae, free (%) 0.611 ± 0.263 0.515 ± 0.183 0.915 (0.774, 1.08)
Ae, total (%)§ 3.04 ± 0.777 2.59 ± 0.771 0.892 (0.796, 1.00)
*

Median (ranges).

Not significant.

Percentage of the bupropion dose excreted as free (unconjugated) form of 4-hydroxybupropion in the 24 h urine.

§

Percentage of the bupropion dose excreted as total form of 4-hydroxybupropion in the 24-h urine.