Use of Fluorine 18 in Nuclear Medicine
Fluorine 18 is a positron emitter with a half life of 109.77 minutes. It is used in PET scans.
Decay mode: 9F18 ( 8O18 + +1e0 (1.656 MeV). Oxygen 18 is stable. The positron travels only a few millimetres in the human body before it meets an electron, when both are annihilated producing two gamma ray photons. The energy of each gamma ray photon is 511 MeV, the rest mass of the electron, so presumably the positron looses some energy prior to annihilation. The typical exposure from a PET scan is about 7 mSv.
Production: Irradiation of the stable oxygen 18 isotope with high energy protons (18 MeV) from a cyclotron. 8O18 + +1p1 ( 9F18 + 0n1. The target is either normal or enriched water.
Half life: 109.77 minutes, which means that the radioisotope must be transported post haste. Ideally a nuclear medicine facility at a hospital would have its own cyclotron.
Fluorine is used as a radioactive tracer in PET Scans mostly as Fluorodeoxyglucose (more precisely 2-Deoxy-2-fluoro-D-glucose or FDG for short), which is a glucose analogue and is taken up by body cells that are high users of glucose such as brain and cancer cells. The presence of Fluorine in the molecule inhibits the body metabolising it as a normal glucose molecule. Once the Fluorine has decayed to Oxygen 18 the normal metabolic process proceeds. A typical dose is 5 - 10 millicuries or 200 to 400 MBq administered by saline drip. The patient is scanned an hour later during which the patient should avoid activity so that the FDG does not go to active muscles.
Flumazenil (C15H14FN3O3 ) inhibits the action of benzodiazepines such as Librium and Valium, which have a slowing down effect on the central nervous system, they are used in the treatment of insomnia, seizures and alcohol withdrawal. Flumazenil is mostly used with patients who become excessively drowsy with benzodiazepines, and sometimes in the...
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