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Table 2 Pharmacokinetic parameters (mean ± SD) for meperidine following a single IV administration of meperidine HCl (0.25, 0.5 and 1.0 mg/kg) to adult horses. All values reported were generated using non-compartmental analysis

From: Meperidine pharmacokinetics and effects on physiologic parameters and thermal threshold following intravenous administration of three doses to horses

Parameters

Dose Groups

0.25 mg/kg

(n = 7)

0.5 mg/kg

(n = 8)

1.0 mg/kg

(n = 8)

C(0) ng/mL

540.9 ± 142.9c

691.9 ± 123.1c

987.7 ± 224.6ab

Lambdaz(1/h)

0.358 ± 0.157b

0.245 ± 0.139a

0.207 ± 0.062

HL Lambdaz (h)

1.93 ± 1.39c

2.82 ± 2.10

3.35 ± 0.940a

Vdss (L/kg)

0.829 ± 0.138bc

1.08 ± 0.194ac

1.58 ± 0.280ab

CL (mL/min/kg)

18.0 ± 1.40c

19.3 ± 3.03c

22.8 ± 3.60ab

AUC0 − inf (h*ng/mL)

232.7 ± 19.4bc

442.8 ± 73.1ac

748.3 ± 125.5ab

  1. C(0) Concentration extrapolated to the origin, Lambdaz, terminal slope; HL Lambdaz, terminal half-life, Vdss Volume of distribution at steady-state, CL Clearance, AUC0 − inf, Area under the plasma-concentration curve from time 0 to infinity
  2. asignificantly different (p < .05) from 0.25 mg/kg 
  3. bsignificantly different (p < .05) from 0.5 mg/kg
  4. csignificantly different (p < .05) from 1.0 mg/kg