Radionuclide Imaging & Therapy

01Radionuclide Imaging & Therapy

Radioactive Tracers

This section covers the properties and uses of radioactive tracers, radiopharmaceuticals, technetium-99m, iodine-131, indium-111 and the molybdenum–technetium generator.

Using tracers inside the body

A radioactive tracer is a radioactive substance introduced into the body so that the distribution or activity of particular tissues and organs can be investigated.

The radioisotope can be attached to a molecule that is naturally taken up by a particular tissue. A molecule labelled in this way forms a radiopharmaceutical.

The radiopharmaceutical should travel through the body without significantly changing the process being investigated. Its chemical properties determine where it accumulates, while its radioactive decay makes the distribution detectable outside the patient.

Properties of a useful diagnostic tracer

  • It should emit gamma radiation so photons can escape from the body and be detected externally.
  • The gamma photons should have enough energy to leave the body while unnecessary ionisation is kept low.
  • The physical half-life should be short enough to limit prolonged irradiation but long enough for the investigation to be completed.
  • The isotope must be capable of labelling a compound with an affinity for the organ or process being investigated.

Technetium-99m

Technetium-99m is a widely used diagnostic tracer. It emits gamma radiation of about 140keV140\,\text{keV} and has a physical half-life of about 66 hours.

Its chemistry allows it to label many different radiopharmaceuticals, so it can be used to investigate a wide range of organs, blood flow and tumours.

Iodine-131

Iodine-131 has a physical half-life of about 88 days and emits both gamma radiation and β\beta^- particles.

Iodine is absorbed by the thyroid, making this isotope useful for investigation and treatment of thyroid tissue.

Indium-111

Indium-111 is a gamma emitter with a physical half-life of about 6868 hours.

It can label antibodies and blood cells, making it useful for locating infections and investigating some blood disorders and uncommon tumours.

Tracer Radiation Physical half-life Gamma energy Example use
Technetium-99m γ\gamma 66 h 140keV140\,\text{keV} Many organs, blood flow and tumours
Iodine-131 β\beta^- and γ\gamma 88 d about 360keV360\,\text{keV} Thyroid investigation and treatment
Indium-111 γ\gamma 6868 h about 170170 and 250keV250\,\text{keV} Labelling antibodies and blood cells

The molybdenum–technetium generator

The short 66-hour half-life of technetium-99m is useful for reducing patient exposure, but it also means the isotope cannot conveniently be produced far from the hospital and stored for long periods.

Molybdenum-99 has a longer physical half-life of about 6666 hours and decays to produce technetium-99m. This makes it practical to transport molybdenum-99 to a hospital and generate technetium-99m there when required.

1

Transport

Molybdenum-99 is produced away from the hospital. Its longer half-life allows useful activity to remain during transport.

2

Decay

Inside the hospital generator, molybdenum-99 decays and continuously produces technetium-99m.

3

Extract

A saline solution is passed through the generator so technetium-99m can be collected and prepared for use in a radiopharmaceutical.

The generator combines the transport advantage of the longer-lived parent isotope with the lower patient exposure provided by the short-lived technetium-99m daughter.

What tracer concentration shows

Regions containing more tracer produce more detectable gamma photons, so the resulting image can provide information about function as well as structure.

  • A glucose-labelled tracer can reveal regions with unusually high metabolic activity.
  • Labelled white blood cells can accumulate around an infection.
  • Labelled blood cells can be used to investigate blood distribution.

Exam Tip: When explaining why a tracer is suitable, separate its nuclear properties from its chemical properties. Radiation type, energy and half-life determine detectability and dose; chemical affinity determines where the tracer accumulates.

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