Isotope diagnostics Flashcards

1
Q

What are “in vivo” isotope diagnostics?

How do you call the administered substances?

What type of measurements can you do?

A

host molecule labeled with the radioactive isotope (= radiotracer) that is administered accumulates in the target organ

⇒ either:

  • emitted γ-radiation detected outside the body and the spatial distribution is reconstructed
  • time sequence of the spatial distribution (time change of the activity), the isotope accumulation curve can be calculated by the computer
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2
Q

Describe the aspects of the selection of the isotope that must be considered for in vivo isotope diagnostics?

A
  • only γ emitting isotopes
  • physical half-life should match biological half-life and the time of the measurement, but all as short as possible
  • photon E of the emitted γ-radiation has to be high enough to pass through the parts of the body
  • activity should be high enough to reach the required signal-to-noise ratio, but it should be the lowest possible
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3
Q

What is the biggest advantage of radiotracer technique compared to chemical microanalytical procedures?

A

only concentrations 106 - 108 times lower needed

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4
Q

What is the most common type of isotope generator?

Explain how its isotope is produced.

A

Tc generator (also: Tc cow)

  1. 235U decays to 98Mo
  2. 98Mo bombarded with neutrons → 99Mo produced (= “parent” isotope)
  3. 99Mo undergoes β-decay with 66h half-life → excited, metastable 99mTc produced (= “daughter” isotope)
  4. nuclear isomerism: 99mTc loses excess energy (γ-radiation) with 6h half-life → 99Tc

99mTc must be seperated chemically to get an isotope which emits soft, monochromatic, purely γ-radiation

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5
Q

Explain how 99mTc is chemically seperated from Mo.

Draw the structure of a Tc generator.

A
  1. Mo applied in form of a water insoluble ammonium molibdenate (NH4MoO4) carrier compound
  2. adsorbed to aluminium oxide (Al2O3) granules and placed into generator column
  3. NH4MoO4 decays to ammonium pertechnetate (NH4mTcO4)
  4. elution: NaCl-containing solution drained up through the column by upper vacuum vial
  5. NH4+ ions exchange with Na+water soluble NamTcO4 produced

⇒ γ-radiating 99mTc washed off → gets into vacuum vial (removable and used for diagnostics)

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6
Q

What is the initial activity of Mo?

Explain the time course of the formation and elution of the mTc in the Tc generator using a graph.

A

initial activity of Mo = 5 GBq

mTc can be “milked” every 24h for about one week with decreasing activites

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7
Q

How do you call the organic carrier compound where the isotope is attached in order to administer it?

A

radiopharmaceutical

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8
Q

Explain the different types of half-life.

Why are they an important aspect of the selection of isotopes?

Relate them in one graph.

A
  • physical half-life (Tphys): in vitro half-life
  • biological half-life (Tbiol): half-life in organism if there was no physical decay
  • effective half-life (Teff): Tphys + Tbiol

diagnostic relevance:

⇒ Tphys not too short, would end before end of examination

⇒ Tphys not too long, would cause unwanted exposure

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9
Q

Which photon energies are used in practice for isotope diagnostics?

Why?

A

Eγ > 100 keV

⇒ if E too low, radiation absorbed by the tissue

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10
Q

Which activities are used in practice for isotope diagnostics?

Why?

What does it depend on?

A

1 - 100 MBq

⇒ minimal activity depends on signal-to-noise ratio of the measuring device (if low ratio, lower activity needed)

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11
Q

What is the difference btw dynamic and static examinations?

A
  • static examinations: spatial distribution of isotope measured
  • dynamic examinations: time dependence of activity measured (2+ measurements)
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12
Q

What is an isotope accumulation curve?

Draw the graph and explain its different regions.

What are the most important parameters that can be taken from it?

A

represents time dependence of the activity (in fractions) in the organ

  • lag time: time until appearance of the activity T0
    transport capacity to the organ
  • ascending slope = clearance
    ⇒ uptake rate of the organ
  • Tmax: time until reaching maximum activity
    uptake + elimination activity, esp. important when paired organs are compaired
  • descending slope = decay + elimination
    ⇒ Teff, Tbiol can be calculated
  • integral: mean isotope content
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13
Q

Why is the size of the collimator hole relevant for the measurement?

A

smaller hole → higher resolution

more precise location of isotopes since only parallel γ-photons measured

bigger hole → higher sensitivity

lower activity needed since more γ-photons are measured

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14
Q

What is a scintigraph?

A
  • detector equipped with a single collimator hole scans the examined area
  • activity values measured at different locations are recorded by a plotter device moving parallel with the detector
  • spots of different sizes (brightness or color) resemble activity at the corresponding locations
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15
Q

What is a gamma camera?

What is a SPECT?

Draw a gamma camera.

A

Gamma camera:

  • collimator plate (numerous holes), a large size scintillation crystal and several PMTs
  • computer reconstructs 2D image

SPECT:

  • Single Photon Emission Computed Tomography
  • 1+ gamma camera measuring heads
  • pictures from different directions ⇒ 3D image
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16
Q

What is a PET?

What is its main advantage over a gamma camera or SPECT?

A

Positron Emission Tomography

  1. β-radiating isotope administered
  2. annihilation occurs when e+ and e- collide → 2 γ-photons of 511 keV produced that travel into opposite directions
  3. detected by detectors in a ring around the patient
  4. coincidence of the detected photons analyzed andlocation of the decays located → 2D or 3D image (if several rings) constructed

very sensitive since no collimators used, but image is constructed according to differences in the timing of γ-photons striking the detectors

17
Q

Draw the graph of the experimental setup used for the measurement.

A