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. 2014 May 22;14(2):125–132. doi: 10.1007/s40268-014-0047-7

Table 3.

Pharmacokinetic parameters for buspirone and 1-(2-pyrimidinyl)-piperazine after either F1 or F2 administration

Dosing C max (ng/mL) T max (h) AUC(0–1,590) (ng*h/mL) AUC extrapolated(0–∞) (ng*h/mL) Tlag (h) T ½ (h)
F1 buspirone (ng/mL) 3.95 ± 4.38 3.69 ± 0.54 7.63 ± 8.07 8.02 ± 8.57 2.96 ± 0.14 6.03 ± 2.27
F2 buspirone (ng/mL) 2.16 ± 2.55 3.95 ± 1.82 5.14 ± 5.08 5.56 ± 5.24 3.33 ± 0.82 7.12 ± 2.33
F1 1-(2-pyrimidinyl)-piperazine (ng/mL) 4.35 ± 1.65 4.02 ± 0.68 25.4 ± 14.60 27.4 ± 17.8 3.27 ± 0.33 4.84 ± 2.11
F2 1-(2-pyrimidinyl)-piperazine (ng/mL) 3.99 ± 1.71 4.40 ± 2.27 21.6 ± 6.7 22.7 ± 7.4 3.58 ± 1.32 4.86 ± 1.66

The values are mean ± SD. The means of F1 are calculated with the data of 13 women and the means of F2 are based on the data of 12 women

AUC area under the curve, C max maximum concentration, Tlag absorption lag time, T max time to maximum concentration, T ½ half-life