Table 1 lists certain medical diagnostic uses of radiopharmaceuticals, including isotopes and activities that are typically administered. Many organs can be imaged with a variety of nuclear isotopes replacing a stable element by a radioactive isotope. One common diagnostic employs iodine to image the thyroid, since iodine is concentrated in that organ. The most active thyroid cells, including cancerous cells, concentrate the most iodine and, therefore, emit the most radiation. Conversely, hypothyroidism is indicated by lack of iodine uptake. Note that there is more than one isotope that can be used for several types of scans. Another common nuclear diagnostic is the thallium scan for the cardiovascular system, particularly used to evaluate blockages in the coronary arteries and examine heart activity. The salt TlCl can be used, because it acts like NaCl and follows the blood. Gallium-67 accumulates where there is rapid cell growth, such as in tumors and sites of infection. Hence, it is useful in cancer imaging. Usually, the patient receives the injection one day and has a whole body scan 3 or 4 days later because it can take several days for the gallium to build up.

Note that Table 1 lists many diagnostic uses for 99mTc99mTc size 12{"" lSup { size 8{"99m"} } "Tc"} {}, where “m” stands for a metastable state of the technetium nucleus. Perhaps 80 percent of all radiopharmaceutical procedures employ 99mTc99mTc size 12{"" lSup { size 8{"99m"} } "Tc"} {} because of its many advantages. One is that the decay of its metastable state produces a single, easily identified 0.142-MeV γγ ray. Additionally, the radiation dose to the patient is limited by the short 6.0-h half-life of 99mTc99mTc. And, although its half-life is short, it is easily and continuously produced on site. The basic process for production is neutron activation of molybdenum, which quickly ββ decays into 99mTc99mTc. Technetium-99m can be attached to many compounds to allow the imaging of the skeleton, heart, lungs, kidneys, etc.

Figure 2 shows one of the simpler methods of imaging the concentration of nuclear activity, employing a device called an Anger camera or gamma camera. A piece of lead with holes bored through it collimates γγ size 12{γ} {} rays emerging from the patient, allowing detectors to receive γγ size 12{γ} {} rays from specific directions only. The computer analysis of detector signals produces an image. One of the disadvantages of this detection method is that there is no depth information (i.e., it provides a two-dimensional view of the tumor as opposed to a three-dimensional view), because radiation from any location under that detector produces a signal.

Figure 2: An Anger or gamma camera consists of a lead collimator and an array of detectors. Gamma rays produce light flashes in the scintillators. The light output is converted to an electrical signal by the photomultipliers. A computer constructs an image from the detector output.

Imaging techniques much like those in x-ray computed tomography (CT) scans use nuclear activity in patients to form three-dimensional images. Figure 3 shows a patient in a circular array of detectors that may be stationary or rotated, with detector output used by a computer to construct a detailed image. This technique is called single-photon-emission computed tomography(SPECT) or sometimes simply SPET. The spatial resolution of this technique is poor, about 1 cm, but the contrast (i.e. the difference in visual properties that makes an object distinguishable from other objects and the background) is good.

Figure 3: SPECT uses a geometry similar to a CT scanner to form an image of the concentration of a radiopharmaceutical compound. (credit: Woldo, Wikimedia Commons)

Images produced by β+β+ emitters have become important in recent years. When the emitted positron ( β+β+) encounters an electron, mutual annihilation occurs, producing two γγ rays. These γγ rays have identical 0.511-MeV energies (the energy comes from the destruction of an electron or positron mass) and they move directly away from one another, allowing detectors to determine their point of origin accurately, as shown in Figure 4. The system is called positron emission tomography (PET). It requires detectors on opposite sides to simultaneously (i.e., at the same time) detect photons of 0.511-MeV energy and utilizes computer imaging techniques similar to those in SPECT and CT scans. Examples of β+β+ size 12{β rSup { size 8{+{}} } } {} -emitting isotopes used in PET are 11C11C size 12{"" lSup { size 8{"11"} } C} {}, 13N13N size 12{"" lSup { size 8{"13"} } N} {}, 15O15O size 12{"" lSup { size 8{"15"} } O} {}, and 18F18F, as seen in Table 1. This list includes C, N, and O, and so they have the advantage of being able to function as tags for natural body compounds. Its resolution of 0.5 cm is better than that of SPECT; the accuracy and sensitivity of PET scans make them useful for examining the brain’s anatomy and function. The brain’s use of oxygen and water can be monitored with 15O15O. PET is used extensively for diagnosing brain disorders. It can note decreased metabolism in certain regions prior to a confirmation of Alzheimer’s disease. PET can locate regions in the brain that become active when a person carries out specific activities, such as speaking, closing their eyes, and so on.

Figure 4: A PET system takes advantage of the two identical γγ size 12{γ} {}-ray photons produced by positron-electron annihilation. These γγ size 12{γ} {} rays are emitted in opposite directions, so that the line along which each pair is emitted is determined. Various events detected by several pairs of detectors are then analyzed by the computer to form an accurate image.