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. 2001 Dec;52(6):671–680. doi: 10.1046/j.1365-2125.2001.01496.x

Table 5.

Comparison of the posterior Bayesian estimates of the pharmacokinetic parameters (mean ± s.d.) of AmB administered in dextrose and AmB administered in lipid emulsion.

Parameter Dextrose (n = 57) Lipid (n = 65) Significance1
Weight (kg) 23.3 ± 11.3 21.4 ± 10.5 NS
CL (l h–1) 0.79 ± 0.23 0.96 ± 0.24 P < 0.005
CL (l h–1kg–1) 0.038 ± 0.015 0.052 ± 0.021 P < 0.0005
V (l) 8.51 ± 3.26 9.72 ± 4.24 NS
V (l kg–1) 0.41 ± 0.20 0.58 ± 0.43 P < 0.05
Vss (l kg–1) 1.18 ± 0.57 1.74 ± 1.35 P < 0.05
t1/2 λ1 (h) 1.46 ± 0.33 1.45 ± 0.26 NS
t1/2 λz (h) 26.4 ± 11.6 26.1 ± 12.8 NS
k12 (h–1) 0.28 ± 0.13 0.28 ± 0.14 NS
k21 (h–1) 0.15 ± 0.05 0.14 ± 0.03 NS
MRT (h) 33.0 ± 15.5 32.4 ± 17.8 NS

s.d.=standard deviation.

1

The pharmacokinetics of AmB infused in dextrose and lipid emulsion were compared using the Mann–Whitney-U-test.