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Table 3 Pharmacokinetic and pharmacodynamic parameters a for ampicillin (AMP) and azithromycin (AZM) following a single intravenously administered dose of both drugs 18 h post infection

From: Combination therapy with ampicillin and azithromycin in an experimental pneumococcal pneumonia is bactericidal and effective in down regulating inflammation in mice

Parameters

  

(Mean ± SD)

Ampicillin

Azithromycin

Pharmacokinetics

Dose (mg/kg)

200

50

Cmax (μg/ml)

4586 ± 22.3

8.9 ± 0.26

Cmin (μg/ml)

16.25 ± 0.9

2.1 ± 0.18

AUC0-6 (μg.h/ml)

111265 ± 14610

15310 ± 1215.86

t1/2 (h)

0.963 ± 0.03

16.5 ± 1.56

Ke (h-1)

0.057 ± 0.013

0.19 ± 0.002

Pharmacodynamics

AUC/MIC (h)

3477.03

32.24

T > MIC (h)

6.741

5.1

Cmax/MIC

143.31

1.11

  1. aAbbreviations: Cmax maximum concentration of drug in serum, Cmin minimum concentration of the drug in serum, t1/2 time taken to reach half of the maximum concentration, AUC area under the concentration-time curve from time zero to 6 h post antibiotic treatment, K e - Elimination rate of the drug, T >MIC Time during which the drug concentration remains above the MIC value in serum, AUC/MIC Ratio of area under the curve during 6 h of post antibiotic treatment to the MIC value for the S. pneumoniae strain AMRI-SP1, C max /MIC ratio of maximum concentration of the drug achieved in serum to MIC of the drug.