Modele kompartmentowe: Model dwukomorowy

The two-compartment model accounts for varying blood perfusion rates among organs and tissues. The central compartment includes blood and highly perfused tissues where drugs distribute rapidly, while the peripheral compartment contains tissues with slower drug distribution. This division reflects the reality that drug distribution is not uniform throughout the body.

Following a single IV bolus dose, drug concentration is initially high in plasma and low in tissues. The drug concentration rapidly declines in plasma while simultaneously increasing in tissues as distribution occurs. This rapid initial decline represents the distribution or alpha phase of plasma concentration change.

Drug distribution between the central and peripheral compartments is a first-order process defined by rate constants termed transfer constants or micro constants. These constants govern how quickly drug molecules move from highly perfused tissues to slower-perfused tissues, controlling the rate and extent of drug redistribution throughout the body.

Once equilibrium is reached between central and peripheral compartments, drug concentration stops changing due to distribution. After this point, both compartments experience a slow, simultaneous decline in drug concentration due to elimination processes. This slower phase is called the elimination or beta phase.

Plasma drug concentration declines bi-exponentially because two distinct processes occur sequentially. The rapid initial decline represents the distribution or alpha phase as drug moves from plasma to tissues. The subsequent slower decline represents the elimination or beta phase after equilibrium is established and drug is removed from both compartments.

The two-compartment model recognizes that blood perfusion rates vary among different organs and tissues, preventing uniform drug distribution. By dividing the body into central and peripheral compartments with different distribution rates, the model accurately predicts how drug concentration changes over time in plasma and tissues, rather than assuming instantaneous equilibrium.

Transfer constants, also called micro constants, quantify the rate of drug movement between central and peripheral compartments during the first-order distribution process. These constants determine how quickly drug redistributes from highly perfused tissues to slower-perfused tissues and influence the duration and shape of the distribution phase in plasma concentration profiles.