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Twilite Calibration

In experiments using the twilite and a PET system is necessary to cross-calibrate the two devices. This means, that the count-rate of coincidences which the twilite measures for a tracer concentration in the catheter needs to be converted into the activity concentration which the PET measures for the same tracer concentration in the field-of-view.

In principle, the following is done for the calibration:

  1. PET tracer is added to water such that the activity concentration is in the range of 200-500 kBq/cc. Note that the same isotope should be used as in the actual live experiments. The reason is the variability of the branching factor, which is accounted for during the calculation of the tracer concentration by the PET system. While the standard PET isotopes have branching factors above 0.95, is is lower for Cu-64 (0.174) and Ga-68 (0.891).
  2. A catheter of the type used in the live experiment is filled with the fluid.
  3. A PET phantom is filled with the same fluid.
  4. The catheter is measured in the twilite, producing the rate of coincidences in counts/sec. The geometry of the catheter loop in the measuring head needs to be exactly the same as in the experiment. This is achieved by inlaying the catheter in a precision templates which Swisstrace delivers for the different catheter diameters.
  5. At the same time the phantom is measured in the PET system, the data corrected and reconstructed in the same was as in the live experiment, resulting in a tracer concentration in kBq/cc.
  6. The calibration factor is finally calculated by diving the PET concentration by the twilite count-rate:
    F = CPET/Rtwilite
    and has units (kBq/cc)/(counts/sec).

In practice, the calibration has to cope with the following challenges:

Recommendation: Although it was found that the calibration factor is quite stable over time, it is recommend to perform a new calibration for every live experiment.

In This Section

Calibration Experiment

Calibration Processing