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. 2017 Apr 17;5(3):e00305. doi: 10.1002/prp2.305

Table 7.

Using C max as a dose surrogate to predict plasma dosimetry of TCM in humans

GT solids and PE pharmacokinetic studies in humans Predicted and actual C max in the plasma (μg/mL) Total TCM concentration in the plasma (μg EGCg equivalents/mL)d Administered TCM dose metrics (mg EGCg equivalents/kg)e
EGCG EGC EC
Lee et al. (2002); 20 mg/kg GT solids 0.06a (0.08)b 0.07 (0.22)c 0.04 (0.12)c 0.20 6.06
Chow et al. (2005); 400 mg PE 0.11 (0.14) 0.01 (0.02) 0.01 (0.00) 0.13 8.42
Chow et al. (2001); 600 mg PE 0.21 (0.17) 0.02 (0.01) 0.01 (0.01) 0.21 12.46
Chow et al. (2005); 800 mg PE 0.21 (0.29) 0.02 (0.03) 0.01 (0.00) 0.25 15.71
Chow et al. (2005); 1200 mg PE 0.35 (0.92)c 0.04 (0.04) 0.02 (0.01) 0.42 26.70
a

Values without brackets are predicted C max of unchanged TCs based on PBPK modeling.

b

Bracketed values are C max from the literature. These C max usually are determined from free tea catechin concentrations except those of Lee et al. (2002) study, which are determined from total tea catechin concentrations (free plus conjugated forms).

c

Cmax is under‐predicted when compare with the observed value.

d

Total TCM concentrations are expressed as μg EGCg equivalents/mL plasma; they are calculated using predicted C max and the concentration/dose additivity model (ATSDR, 2004).

e

Administered dose metrics are expressed as mg EGCg equivalents/kg BW; they are calculated using the concentrations of individual TCs in PE and the additivity model (ATSDR, 2004).