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. 2005 Jun;49(6):2528–2532. doi: 10.1128/AAC.49.6.2528-2532.2005

TABLE 3.

Pharmacokinetic-parameters of clarithromycin after oral administration at a dose of 20 mg/kg to rats with DMIA and DMIS and their respective control ratsa

Parameter Value for:
DMIA control rats (n = 11) Rats with DMIA (n = 9) DMIS control rats (n = 9) Rats with DMIS (n = 10)
Body weight (g)
    Initialb 248 ± 7.17 252 ± 6.12 248 ± 5.65 257 ± 10.6
    Finalc 271 ± 7.69 234 ± 8.94d 286 ± 20.4 236 ± 20.4d
AUC0-∞ (μg · min/ml) 113 ± 33.8 74.9 ± 34.7e 121 ± 44.1 85.9 ± 24.4e
Terminal half-life (min) 190 ± 104 214 ± 88.4 173 ± 44.0 112 ± 43.4e
Cmax (μg/ml) 0.462 ± 0.113 0.414 ± 0.171 0.607 ± 0.205 0.655 ± 0.232
CLR (ml/min/kg) 14.3 ± 5.21 15.4 ± 6.10 16.0 ± 10.3 24.2 ± 11.9
Tmax (min) 53.2 ± 52.1 36.7 ± 26.1 21.7 ± 10.9 27.0 ± 15.5
Ae0-24 h (% of dose) 8.58 ± 2.54 6.46 ± 4.05 10.4 ± 3.45 11.5 ± 3.74
GI24 h (% of dose) 0.363 ± 0.437 1.23 ± 1.07 0.752 ± 1.02 1.36 ± 1.25
F (%) 22.5 20.2 21.0 19.7
a

Values shown are means ± standard deviations.

b

Measured just before injection of alloxan, streptozotocin, or respective vehicles.

c

Measured just before starting the experiment.

d

P < 0.001 compared with the control.

e

P < 0.05 compared with the control.