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. 2018 Aug 31;9:895. doi: 10.3389/fphar.2018.00895

Table 3.

Main pharmacokinetic parameters of caffeine, dapsone, and chlorzoxazone in rat plasma.

Probe drug Pharmacokinetics Control group Experimental group
Caffeine t1/2(h) 6.76 ± 3.59 4.06 ± 1.99
Cmax (mg L-1) 9.92 ± 1.82 7.06 ± 1.66∗∗
AUC(0-∞) (mg L-1 h) 77.50 ± 16.88 31.75 ± 5.35∗∗
MRT(0-∞) (h) 8.05 ± 2.02 5.50 ± 1.59
CL (L h-1 kg-1) 0.13 ± 0.03 0.32 ± 0.06∗∗
Dapsone t1/2 (h) 11.58 ± 4.72 8.59 ± 3.52
Cmax (mg L-1) 1.74 ± 0.39 2.01 ± 0.69
AUC(0-∞) (mg L-1 h) 33.52 ± 8.10 22.83 ± 3.46∗∗
MRT(0-∞) (h) 17.94 ± 6.60 12.1 ± 4.03
CL (L h-1 kg-1) 0.31 ± 0.08 0.45 ± 0.06∗∗
Chlorzoxazone t1/2 (h) 1.29 ± 0.95 0.98 ± 0.63
Cmax (mg L-1) 10.90 ± 2.25 9.56 ± 1.50
AUC(0-∞) (mg L-1 h) 39.74 ± 3.97 22.71 ± 3.91
MRT(0-∞) (h) 3.42 ± 0.25 4.53 ± 1.58
CL (L h-1 kg-1) 0.51 ± 0.05 0.90 ± 0.16

t1/2, half-life; Cmax, the peak or maximum concentration; AUC(0-∞), area under a curve extrapolated to infinity; MRT(0-∞), mean residence time; CL, the total body clearance. Values are presented as mean ± SD (n = 6).P < 0.05 when compared with related parameters of control group. ∗∗P < 0.01 when compared with related parameters of control group.