Lesson plan
Patlak plot
A Patlak plot (sometimes called Gjedde–Patlak plot, Patlak–Rutland plot, or Patlak analysis) is a graphical analysis technique based on the compartment model that uses linear regression to identify and analyze pharmacokinetics of tracers involving irreversible uptake, such as in the case of deoxyglucose. It is used for the evaluation of nuclear medicine imaging data after the injection of a radioopaque or radioactive tracer. The method is model-independent because it does not depend on any specific compartmental model configuration for the tracer, and the minimal assumption is that the behavior of the tracer can be approximated by two compartments – a "central" (or reversible) compartment that is in rapid equilibrium with plasma, and a "peripheral" (or irreversible) compartment, where tracer enters without ever leaving during the time of the measurements. The amount of tracer in the region of interest is accumulating according to the equation: : R(t) = K \int_0^t C_p(\tau) \, d\tau + V_0 C_p(t) where t represents time after tracer injection, R(t) is the amount of tracer in region of interest, C_p(t) is the concentration of tracer in plasma or blood, K is the clearance determining the rate of entry into the peripheral (irreversible) compartment, and V_0 is the distribution volume of the tracer in the central compartment.…
Article summary
A Patlak plot (sometimes called Gjedde–Patlak plot, Patlak–Rutland plot, or Patlak analysis) is a graphical analysis technique based on the compartment model that uses linear regression to identify and analyze pharmacokinetics of tracers involving irreversible uptake, such as in the case of deoxyglucose. It is used for the evaluation of nuclear medicine imaging data after the injection of a radioopaque or radioactive tracer. The method is model-independent because it does not depend on any specific compartmental model configuration for the tracer, and the minimal assumption is that the behavior of the tracer can be approximated by two compartments – a "central" (or reversible) compartment that is in rapid equilibrium with plasma, and a "peripheral" (or irreversible) compartment, where tracer enters without ever leaving during the time of the measurements. The amount of tracer in the region of interest is accumulating according to the equation: : R(t) = K \int_0^t C_p(\tau) \, d\tau + V_0 C_p(t) where t represents time after tracer injection, R(t) is the amount of tracer in region of interest, C_p(t) is the concentration of tracer in plasma or blood, K is the clearance determining the rate of entry into the peripheral (irreversible) compartment, and V_0 is the distribution volume of the tracer in the central compartment.…
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Discussion questions
- Summarise the article in your own words. Which single claim would you verify first, and why?
- Which claim in this article is most likely to be revised as the sources update? How would you check its current status?
- If two sources disagreed about one of these facts, what would you need in order to trust one over the other?
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