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. 2017 Jul 7;24(1):1037–1044. doi: 10.1080/10717544.2017.1346002

Table 1.

Comparisons of kinetic profile of orally, intranasally and intravenously administered borneol in mice using the noncompartmental model.

  i.v. i.n. p.o.
Plasmaa      
 Cmax (μg/mL) 68.0 ± 8.4 25.9 ± 5.0** 15.6 ± 2.3**
 Tmax (min) 1.0 3.0 10.0
AUC0–120 min (μg·mL−1·min) 632.3 ± 50.8 573.4 ± 77.7 271.8 ± 37.4**
MRT0–120 min (min) 12.2 ± 1.6 28.2 ± 1.4** 17.9 ± 2.1**
 F (%) 100 90.7 43.0
Brain      
 Cmax (μg/g) 43.0 ± 5.1 9.0 ± 1.4** 8.5 ± 2.0**
 Tmax (min) 1.0 3.4 10.0
AUC0–120 min (μg·g−1·min) 505.3 ± 82.9 345.5 ± 70.0* 194.0 ± 23.5**
MRT0–120 min (min) 20.5 ± 8.8 49.0 ± 8.3** 43.6 ± 17.1**
 Re (%) 100 68.4 38.4
 Te (%) 79.9 60.3 71.4
DTI 1.0 0.8 0.9

This table is modified based on Zhao et al. (2012). Data are expressed as mean ± SD (n = 5). *p < 0.05, **p < 0.01: versus intravenous group, using one-way analysis of variance (ANOVA). i.v.: intravenous administration; i.n.: intranasal administration; p.o.: oral administration; Cmax: calculated maximum concentration; Tmax: time corresponding to Cmax; AUC0–120 min: partial area under the curve from 0 to 120 min; MRT0–120 min: mean residence time from 0 to 120 min; F: absolute bioavailability; Re: relative brain targeted coefficient; Te: brain/blood drug ratio; DTI: drug target index.