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. Author manuscript; available in PMC: 2018 Oct 1.
Published in final edited form as: Drug Alcohol Depend. 2017 Aug 8;179:347–354. doi: 10.1016/j.drugalcdep.2017.07.011

Table 3.

Serum pharmacokinetic parameters after a 1.5 mg/kg iv dose of (S)-MDPV or (R)-MDPV in female and male rats. Also, see the representative concentration-time plots in Figure 3. Note that the single enantiomer dose of 1.5 mg/kg is equivalent to its respective enantiomer in a 3 mg/kg (R,S)-MDPV dose. See supplemental files for more details of the statistical analysis.

(S)-MDPV (R)-MDPV S/R ratio
Dose and PK Parameter Female Male Female Male Female Male
1.5 mg/kg (R,S)-MDPV n = 5 n = 4 n = 5 n = 4 n = 5 n = 4
AUCInf (ng min/ml)/dosea 14989 ± 1831 20108 ± 10088 20935 ± 5079 16492 ± 7447 0.74 ± 0.17 b 1.30 ± 0.45
t1/2λz (min)c 84 ± 20 95 ± 29 91 ± 31 121 ± 66 0.97 ± 0.39 0.76 ± 0.21
ClT (ml/min/kg) 67 ± 8 57 ± 19 50 ± 12 72 ± 33 1.40 ± 0.34 0.87 ± 0.40
Vdss (l/kg) 3.4 ± 1.6d 1.9 ± 0.7 1.6 ± 0.6 2.7 ± 1.1 2.06 ± 0.52 b 0.74 ± 0.25
Vd (l/kg) 8.8 ± 2.9 8.9 ± 4.3e 7.0 ± 2.7f 15.4 ± 8.3 1.38 ± 0.70 0.60 ± 0.07
a

Calculated by dividing AUCInf by the 1.5 mg/kg (S)- or (R)-MDPV dose.

b

Significantly different (p < 0.05) from the male S/R ratio value.

c

Harmonic mean and pseudo standard deviation.

d

Significantly different (p < 0.05) from the (R)-MDPV Vdss values within females.

e

Significantly different (p < 0.05) from the (R)-MDPV Vd values within males.

f

Significantly different (p < 0.05) from male (R)-MDPV Vd values.