
- PET radiopharmaceuticals commonly
incorporate short-lived radionuclides of elements encountered in nature, e.g.,
15O (t1/2
= 2 min), 13N (t1/2 = 10 min),
11C
(t1/2 = 20 min), 18F (t1/2 = 110 min).
- Produce no physiological or
pharmacological effects; inherently have a high degree of safety.
- No documented adverse reactions of
clinical significance after hundreds of thousands of studies performed in humans
worldwide.
- Radiation exposure from a PET imaging
procedure is comparable to that of other Nuclear Medicine diagnostic
procedures using gamma-emitting radiopharmaceuticals, many of which have been
in use for decades.
- The radioactive substance used to
evaluate the metabolic or physiologic process must not alter the process it is
attempting to measure.
- Therefore, most substances used in
PET are chemically equivalent or close analogs to naturally occurring
compounds.
- Many PET Radiopharmaceuticals are
radiolabeled version of substances commonly present in the body, e.g.,
13N-ammonia,
15O-water,
11C-acetate,
11C-methionine,
and 18F-FDG
- 18F-FDG is the most
common radiopharmaceutical used in PET worldwide.
- Other PET Radiopharmaceuticals
