Irreversible 2-Tissue Compartment Model, Flux

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Irreversible 2-Tissue Compartment Model, Flux

The irreversible 2-tissue compartment model separates tracer in tissue into two exchanging compartments C1 and C2 with a serial structure. The arterial plasma exchanges with the first tissue compartment C1, which in turn exchanges with the second tissue compartment C2 where the tracer is trapped. K1 [ml/ccm/min] and k2 [1/min] are the uptake and clearance rate constants, whereas k3 [1/min] describes the trapping. The usual interpretation is that C1 represents free and non-specifically bound tracer in tissue (non-displaceable compartment), and C2 irreversibly bound or metabolized tracer.


An important parameter of an irreversible configuration is net influx rate Ki, the unidirectional uptake rate constant that incorporates both net inward transport and trapping of the tracer in tissue.


Another macroparameter "lambda*k3" as been used in the context of enzymatic reactions, where k3 is supposed to be proportional to enzyme concentration.


Logan et al. [1] have shown in simulations that lambda*k3 is preferable to k3 alone in terms of bias and precision.

Differential Equation of the Mass Balance


with input curve Cp(t).

Operational Model Curve


with the concentration CB(t) of tracer in whole blood, and the blood volume fraction vB.

Parameter Fitting

The model includes the 4 fitable parameters vB, K1, Flux, k3, and calculates the LambdaK3 macroparameter. Usually, vB is fixed at a physiologic value of 3-5% to reduce the number of fitted parameters.

Parameter Fitting using Flux instead of k2

The Irreversible 2-Tissue Compartment Model, Flux model variant uses Flux as a fitting parameter instead of k2. The advantage of the reformulation is that the Flux can be calculated as a regression slope with the robust Patlak model, and used as a fixed parameter in the compartment model fit. If the Model Conversion option is enabled, the Flux will be copied when switching from the Patlak model to the Irreversible 2-Tissue Compartment Model, Flux model.


1.Logan J, Fowler JS, Ding YS, Franceschi D, Wang GJ, Volkow ND, Felder C, Alexoff D: Strategy for the formation of parametric images under conditions of low injected radioactivity applied to PET studies with the irreversible monoamine oxidase A tracers [11C]clorgyline and deuterium-substituted [11C]clorgyline. J Cereb Blood Flow Metab 2002, 22(11):1367-1376. DOI