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. 2001 Jun;51(6):531–539. doi: 10.1046/j.0306-5251.2001.01391.x

Table 1.

Pharmacokinetic parameters of oral 6-TG (40 mg m−2) administered in the fasting state and after food. *Subject 6 did not complete the pharmacokinetic study after food and hence was excluded from the analysis.

Fasting After food
Subject Cmax (pmol ml−1) tmax (h) C6 (pmol ml−1) AUC (pmol l−1h) Cmax (pmol ml−1) tmax (h) C6 (pmol ml−1) AUC (pmol ml−1 h)
1 90 1.5 36 286 67 5.0 50 211
2 228 0.5 0 363 194 3.0 0 296
3 496 1.5 28 815 213 3.0 40 613
4 235 1.5 0 320 46 2.0 26 190
5 412 1.5 28 880 168 1.5 0 321
6* 703 1.5 30 1318
7 50 2.5 0 156 16 4.4 0 33
8 737 1.5 46 1306 75 1.5 0 96
9 55 3.1 25 168 18 6.0 18 25
10 391 1.0 50 809 61 4.1 26 117
11 695 1.5 39 1216 103 3.0 36 299
Median 313 1.5 28 586 71 3 22 200
Range 51–737 0.5–3.1 0–50 156–1306 16–213 1.5–6 0–50 25–613