Table 1

Pharmacokinetic parameters of cIgG, nIgG, cFab, and nFab in IPRL

ParametercIgGnIgGcFabnFabpcIgG-nIgGp cFab-nFabp cIgG-cFab
Perfusate
t 1/2λ1(min)5.216  ± 1.62914.72  ± 3.380.0445
t 1/2λz (min)355.07  ± 17.25467.44  ± 11.63552.42  ± 23.70880.15  ± 39.56<0.01<0.01<0.001
V Z (ml)198.66  ± 18.92130.7  ± 10.5204  ± 12.37131.9  ± 0.6<0.05<0.05>0.05
CI h(ml/min)0.425  ± 0.030.2  ± 0.000.275  ± 0.00680.1  ± 0.001<0.01<0.0001<0.01
 AUC0-∞ (min·μg/ml)96.91  ± 11.70196.51  ± 33.4884.47  ± 7.80219.41  ± 39.12<0.05<0.01>0.05
 AUCA(%)1.62  ± 1.350.58  ± 0.3<0.05
E 0.0085  ± 0.00070.004  ± 0.00010.0055  ± 0.000130.002  ± 0.0001<0.01<0.0001<0.01
Bile
 % of dose0.13  ± 0.0010.018  ± 0.0020.223  ± 0.040.17  ± 0.009<0.0001<0.05<0.01

Data are mean ± SE (N = 4).t1/2, half-life; VZ, volume of distribution; CIh, apparent hepatic uptake clearance; AUCA (%), percent of the initial phase AUC to the total AUC; E, hepatic extraction ratio. The statistical differences between cIgG and nIgG, cFab and nFab, and cIgG and cFab are shown as p values.