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. 2017 Jun 14;7:3458. doi: 10.1038/s41598-017-02774-1

Table 3.

The main pharmacokinetic parameters of calycosin, calycosin-7-O-glucoside, formononetin, ononin and mangiferin after the oral administration of PRM (mean ± SD; n = 6).

Parameter Group AUC(0-t) (ng × h/mL) AUC(0-∞) (ng × h/mL) C max (ng/mL) T 1/2 (h) T max (h)
calycosin Normal 66.3 ± 31.5 68.1 ± 32.3 11.2 ± 5.7 4.1 ± 1.7 2.8 ± 1.6
PF 142.9 ± 56.7* 153.5 ± 60.2* 16.3 ± 4.2 6.1 ± 0.9* 2.5 ± 0.8
calycosin-7-O-glucoside Normal 10.2 ± 2.0 28.2 ± 5.3 1.5 ± 1.0 34.7 ± 10.9 0.6 ± 0.4
PF 10.3 ± 3.7 26.0 ± 11.7 1.5 ± 0.8 27.5 ± 15.3 1.3 ± 1.1
formononetin Normal 7.2 ± 3.9 7.7 ± 4.1 2.5 ± 1.8 2.3 ± 1.3 1.3 ± 1.0
PF 6.6 ± 3.1 8.3 ± 4.1 1.6 ± 0.7 6.1 ± 2.1* 1.9 ± 1.0
ononin Normal 24.8 ± 8.1 28.2 ± 9.9 4.9 ± 1.2 5.6 ± 3.2 1.4 ± 0.9
PF 17.1 ± 4.5 18.4 ± 4.8 7.2 ± 2.1 2.4 ± 0.5 0.6 ± 0.4
mangiferin Normal 75.0 ± 27.3 111.9 ± 47.4 16.3 ± 5.9 17.2 ± 11.3 3.0 ± 1.4
PF 20.1 ± 7.6* 25.6 ± 7.8* 4.4 ± 2.2* 10.7 ± 5.2 4.8 ± 2.7

* P < 0.05 compared with the normal group.