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. 2020 Aug 20;64(9):e00533-20. doi: 10.1128/AAC.00533-20

TABLE 3.

Pharmacokinetic data for gentamicin C2 and C2a in rata

Dose (mg/kg) AUC (mg/liter × h)
C2 C2a
10 40 30
30 120 80
100 330 300
a

Repeat measurements were not made to enable a between-experiment statistical analysis, but typical fitting errors for an 8-time-point study to compute values for area under the concentration-time curve (AUC) are higher than the AUC differences observed between C2 and C2a. Plasma protein binding was 84% and 86% unbound for C2 and C2a, respectively.