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. 2019 Apr 29;21(4):61. doi: 10.1208/s12248-019-0323-0

Fig. 1.

Fig. 1

Compartment models for describing hepatic [11C]erlotinib disposition. Xblood, Xliv, Xhep, Xih, and XeBD/GB represent the amount of [11C]erlotinib in the blood, liver tissue, hepatocyte compartment, intrahepatic bile duct, and compartment representing the extrahepatic bile duct and gall bladder, respectively. The rate constants defining the exchange of [11C]erlotinib between blood and liver tissue are defined by k1 (min−1) and k2 (min−1). a In the four-compartment model (4C model), k3 (min−1) is the rate constant describing transfer from liver tissue to the intrahepatic bile duct, and k5 (min−1) is the rate constant describing transfer from the intrahepatic bile duct to the extrahepatic bile duct and the gall bladder. This model is divided into two main regions of interest: the liver, composed of the blood, hepatocyte, and intrahepatic bile duct compartments; and the extrahepatic bile duct and gall bladder (eBD/GB), composed of the extrahepatic bile duct and gall bladder compartment. b In the three-compartment model (3C model), k3 (min−1) is the rate constant describing transfer from the liver to the extrahepatic bile duct and gall bladder. The 3C model is divided into two main regions of interest: the liver, composed of blood and liver tissue compartments; and eBD/GB, which is composed of the extrahepatic bile duct and gall bladder compartment