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. 2016 Mar 17;21(3):367. doi: 10.3390/molecules21030367

Table 3.

Pharmacokinetic parameters of maleic acid after intravenous administration.

Parameters 10 mg/kg, i.v. 30 mg/kg, i.v.
Blood
AIC of one-compartment 18 ± 2 46 ± 2
AIC of two-compartment 25 ± 3 49 ± 2
AUC (min∙µg/mL) 376 ± 33.4 1236 ± 124
Cmax (µg/mL) 10.9 ± 1.08 32.1 ± 5.17
T1/2 (min) 24.1 ± 1.19 28.4 ± 3.20
CL (mL/min/kg) 27.4 ± 2.38 25.3 ± 2.54
MRT (min) 34.7 ± 1.72 40.9 ± 4.62
Vd (mL/kg) 975 ± 113 1050 ± 191
AUC/Dose 37.6 41.2
Kidney
Non-compartment
AUC (min∙µg/mL) 1997 ± 355 6784 ± 1538
Cmax (µg/mL) 41.4 ± 5.04 134 ± 35.6
T1/2 (min) 32.1 ± 5.69 22.3 ± 3.18
CL (mL/min/kg) 5.45 ± 1.06 5.34 ± 1.15
MRT (min) 31.8 ± 1.10 32.7 ± 2.16
Vd (mL/kg) 209 ± 36.5 182 ± 41.9
AUC/Dose 199.7 226.1
AUC ratio of (AUCkidney/AUCblood) 5.31 5.49

Data expressed as mean ± S.E.M. (n = 5). AUC, area under the concentration versus time curve; Cmax, the peak plasma concentration of a drug after administration; T1/2, elimination half-life; CL, total body clearance; MRT, mean residence time; Vd, volume of distribution; the AUC ratio (AUCkidney/AUCblood) in the kidneys and the blood was used to define the distribution of kidney-to-blood maleic acid.