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. 2022 Jun 29;112(3):627–634. doi: 10.1002/cpt.2682

Table 2.

Pharmacokinetic parameters of pseudoephedrine after oral administration with GTE or water in healthy volunteers

Pseudoephedrine Water phase (control) GTE phase
Geometric mean Geo CV (%) Geometric mean Geo CV (%)
C max (ng/mL) 474.8 34.6 407.3 27.4
GMR (90% CI) 0.858 (0.757–0.958)
T max (h) 4.0 (1.5–6.0) 3.5 (1.5–8.0)
AUC0–24 (h ng/mL) 5396.5 37.7 5309.6 36.6
GMR (90% CI) 0.984 (0.931–1.037)
AUC0–∞ (h ng/mL) 5965.8 43.1 6107.8 42.4
GMR (90% CI) 1.024 (0.906–1.142)
t 1/2 (h) 6.5 31.1 7.7 31.6
GMR (90% CI) 1.174 (0.908–1.439)
A e (mg) 68.7 21.0 63.2 20.4
GMR (90% CI) 0.920 (0.846–0.994)
CLR (mL/min) 212.1 53.3 198.3 50.2
GMR (90% CI) 0.935 (0.813–1.058)

Pseudoephedrine (120 mg) was orally administered with water (150 mL), or an aqueous solution of EGCG‐concentrated green tea extract (150 mL) in 10 healthy Japanese volunteers. The T max values are expressed as median (range).

A e, amount excreted unchanged into urine over 24 hours; AUC, area under the plasma concentration‐time curve; CI, confidence interval; CL R, renal clearance; C max, peak plasma concentration; CV, coefficient of variation; GMR, geometric mean ratio; GTE, green tea extract; T max, time to C max; t 1/2, terminal half‐life.