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. Author manuscript; available in PMC: 2020 Jun 1.
Published in final edited form as: Neuropharmacology. 2019 Apr 6;158:107596. doi: 10.1016/j.neuropharm.2019.04.002

Table 4.

Pharmacokinetic constants for carfentanil and norcarfentanil after s.c. administration of 1, 3, or 10 μg/kg carfentanil in male rats.

Analyte Carfentanil
dose
(μg/kg)
Cmax
(pg/mL)
AUC0-8 h
(min*ng/mL)
Ke
(min−1)
t1/2
(min)
Carfentanil 1 (N=6) 613 ± 49 29 ± 3 0.020 ± 0.002 35.4 ± 2.5
3 (N=6) 1902 ± 418 148 ± 25 0.013 ± 0.001* 55.1 ± 6.3
10 (N=5) 7862 ± 804*# 696 ± 184*# 0.012 ± 0.002* 64.4 ± 8.4*
Norcarfentanil 1 (N=6) 40 ± 4 7 ± 1 0.004 ± 0.001 176 ± 10
3 (N=6) 211 ± 38 38 ± 5 0.004 ± 0.001 350 ± 215
10 (N=5) 601 ± 116*# 128 ± 18*# 0.002 ± 0.001 537 ± 200

Data are mean ± SEM for group size given.

Abbreviations are: maximal concentration (Cmax), area-under-the-curve from 0-8 h (AUC0-8 h); elimination rate constant (Ke), and half-life (t1/2)

*

= significant difference compared to 1 μg/kg dose (Tukey’s p<0.05)

#

= significant difference compared to 3 μg/kg dose (Tukey’s, p<0.05)