30. Isotope diagnostics. Flashcards
Isotope diagnostics. Selection principles of radioisotopes.
Explain the importance of isotope diagnostics
Importance of isotope diagnostics:
due to emitted radiation of isotopes organism (metabolism, uptake, excretion, etc.) studied with high sensitivity and reliability
- monitor physiological pathways
- identify, localize pathological changes
What are the selection principles of isotopes used for in-vivo diagnostics? What would be a good isotope for that reason?
Selection principles in in-vivo diagnostics:
- **γ-radiation: **
- least dangerous nuclear radiation (smalles ionization)
- deepest penetration distance (effective range)
-
short half-life:
- should match biological half life and time of measurement
- certain level of activity needed to get a good signal
-
Ephoton ~ 0.1 MeV:
- too long γ-rays → high risk for the body (high absorption), but good for detection
- too short γ-rays → low risk for the body (low absorption), but bad for detection
- part of a biological molecule
- cheap and easily obtained
**→ **99mTc: emits γ-radiation, has short half life (6 hours), E = 0.14 mEv, it can be attached to biological molecules.
How do selection principles of isotopes used for in-vitro diagnostics differ from in-vivo diagnostics? What other differences are there?
Selection principles in in-vitro diagnostics:
- β- and γ-radiation
- half-life may be longer
Aims and other differences:
- usually concentration in body fluid sample determined
- plexi plates are used for radiation protection
Explain what static examinations are
Static examination:
one detection in order to visualize spatial distribution of the radioactive isotope at a certain point of time
Explain what dynamic examinations are
Dynamic examination:
2+ detections in order visualize how spatial distribution of the radioactive isotope changes in time
→ isotope accumulation curve can be obtained
What are the phases in the isotope accumulation curve? Refer to the diagram
Isotope accumulation curve:
after isotope injection:
- lag phase: time until the appearance of the activity (T0) → characterizes the transport capacity to the organ
- clearance: slope of the curve between T and Tmax characterizes the organ → uptake rate of the radioactive isotope
- elimination: decreasing part of the curve → Teff which characterizes the decay of the labeled substance and its elimination from the target organ
→ area under curve gives mean isotope content of the organ during that period
How can half-life be classified? Define the terms and give a formula
Half-lifes:
- phyiscal half-life Tphys: time in which the initial no. of radioactive isotopes decreases by half, because of physical decay
- biological half-life Tbio: time in which the initial no. of radioactive isotopes decreases by half in the body, because of biological process, can be determined if a phantom is applied
- effective half-life Teff: time in which the initial no. of radioactive isotopes decreases by half in the body, because of physical decay and biological processes
→ 1/Teff = 1/Tphys + 1/Tbio
When is a phantom used? What is it?
Determination of Tbio:
Comparison of physical decay of a radioactive isotope outside (= phantom.
additional decrease of the amount of isotope inside the body shoes Tbio