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Thus kinetic modelling techniques are required.
Despite current advances in PET/CT systems, blood sampling still remains the standard method to obtain the radiotracer input function for tracer kinetic modelling.
Importantly, we developed fermentation kinetic modelling for mannosylerythritol lipid production.
Infusion over about 5 min was optimal for kinetic modelling with [18F]FDG in mouse brain.
We have investigated the potential of combined PET-MRI kinetic modelling using simulated FDG data.
Moreover, a comparison, based on intra-observer variability, was made between kinetic modelling and graphical analysis.
Kinetic modelling requires arterial sampling which can be obtained by taking continuous or discrete blood samples.
However, kinetic modelling has also been proposed as an alternative to determine tau binding.
The obtained equilibrium capacities (qe) were then plotted against the equilibrium time for kinetic modelling.
These have to be accounted for in the kinetic modelling.
As kinetic modelling, using non-linear least squares optimisation, is computationally expensive and sensitive to noise, a comparison will be made between kinetic modelling and graphical analysis to quantify [18F]FCho uptake in tissues.
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