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. 2012 Oct 25;7:5565–5575. doi: 10.2147/IJN.S36939

Table 5.

Pharmacokinetic parameters after oral administration of fenofibrate to rats

AUC0→12 h (μg h/mL) Cmax (μg/mL) Tmax (h)
Raw fenofibrate 144.46 ± 61.57 20.52 ± 8.34 3 ± 0.82
Commercial product 635.68 ± 98.14 89.60 ± 12.02 2.63 ± 0.75
Prepared powder (SC3) 667.90 ± 106.29 92.88 ± 7.05 3 ± 0

Note: Data are expressed as mean ± standard deviation (n = 5).

Abbreviations: AUC, area under the curve; Cmax, maximal serum concentration; SC3, supercritical method 3 (fenofibrate:Neusilin UFL2 = 40:60); Tmax, time to peak concentration.