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. 2015 Apr 1;11:84. doi: 10.1186/s12917-015-0400-2

Table 1.

Pharmacokinetic parameters of Praziquantel in grass carp (n = 5)

Plasma Muscle Liver Kidney
Parameter Unit Fresh water Brackish water Fresh water Brackish water Fresh water Brackish water Fresh water Brackish water
Cmax ug/(g or ml) 0.91 0.76 0.62 0.51 3.87 2.70 3.39 2.99
Tmax h 0.5 0.5 0.5 1 0.5 0.5 1 1
t1/2α h 3.25 1.85 0.31 1.12 0.35 2.69 0.76 2.87
t1/2β h 71.15 56.46 44.88 36.17 23.86 15.31 150.23 132.64
t1/2Ka h 0.16 0.028 0.058 0.57 0.15 0.031 0.307 0.64
V1/F L/kg 23.57 30.15 21.53 22.22 28.38 97.33 34.30 87.17
CL/F L/h/kg 0.755 1.042 1.961 0.974 0.481 0.308 1.878 0.350
AUC(0-t) μg/L⋅h 17.951 14.614 8.096 6.865 34.984 44.047 10.411 38.663
AUC(0-∞) μg/L⋅h 26.464 19.189 10.196 20.515 41.547 64.823 10.645 57.132
K10 1/h 0.064 0.035 0.091 0.044 0.17 0.048 0.34 0.16
K12 1/h 0.235 0.212 1.574 0.474 1.469 0.113 2.034 0.754
K21 1/h 0.104 0.14 0.548 0.103 0.355 0.036 0.245 0.042
Ka 1/h 4.201 25.183 11.951 1.203 4.537 22.106 2.26 1.082

Cmax, the peak concentration in plasma; Tmax, the time point of the drug’s maximum plasma concentration; t1/2α, distribution half-life of the drug; t1/2β, elimination half-life of the drug; t1/2Ka, absorption half-life of the drug; V1/F, extensive apparent volume of the central compartment; CL/F, total body clearance of the drug; AUC(0-t), area under the concentration–time curve from 0 h to t; AUC(0-∞), area under the concentration–time curve from 0 h to ∞; K12, K21, first-order rate constants for drug distribution between the central and peripheral compartments; K10, elimination rate constant from the central compartment; Ka, absorption rate constant.