Radio-isotopes in Clinical Medicine

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Radio-isotopes in Clinical Medicine Radiactive isotopes, whether naturally occurring or artificially produced, have a number of different uses in clinical medicine. These include: (1) Diagnostic and research purposes in radiotracer scans (unsealed) (2) As sources for teletherapy and brachytherapy ( sealed) (3) Internal therapeutic administration (unsealed ) Radioisotopes in Diagnosis: Unsealed radioisotopes are normally conjugated with substances which enter into and participate in metabolic pathways-these labeled substances are called radiopharmaceuticals. These can then be followed or imaged by suitable radiation detectors (usually scintillation counter or gamma camera) which detect the gamma rays emitted by the substances inside the body. Selection criteria: (1) Tracer substance should be identical in chemical and biological properties to the corresponding stable substance. (2) The labeling radioisotope should remain firmly attached with the tracer substance throughout the investigation. (3) The radioisotope should have as short a half-life as feasible for the investigation, to reduced unnecessary radiation hazard to the patient. (4) The radioisotope should ideally be a pure gamma-emitter as accompanying beta and alpha rays will only increase the radiation dose without contributing anything to the sensitivity of the scanning process. Thus the best isotopes are radioisomers, ie excited atomic nuclei which retain their gamma energy for some timea further advantage of these molecules are their relatively short half-lives. Technetium 99m is the best radio-isotope for diagnostic purpose, being a pure gamma emitter with a short half-life of only 6 hours. (5) The energy of the isotope should be sufficiently high for it to easily penetrate the body tissues to reach the detector while at the same time being low enough not to create any significant problems with radiation protection. Production of radio-isotopes: In generators/cows. The parent isotopes are kept adsorbed onto Alumina in cylindrical columns inside glass funnels, protected by nylon meshes. The required radioisotopes are usually obtained by washing (or elution) with saline. The parent element for Tc99m is Mo99 and for I32 is Te132.

Type of Test Test Radioisotope Metabolic & physiological Thyroid function test I-131, Renal function I-132 Vit B12 & pernicious Co-57 anemia RBC survival time Cr-51 Detection of melanoma P-32 Total blood volume Cr-51 Plasma volume I-125 Organ visualisation Thyroid I-131, Brain Liver Bone Spleen Cr-51 Radioisotopes in Teletherapy: (All isotopes and/or their daughter products are gamma emitters) Radioisotope Half-life Energy Exposure rate constant (R cm 2 h -1 Ci - Radium 1622 years 0.04-2.45 MeV (avg= 0.83 MeV) 1 ) Production 8.25 Naturally occurring (decay product of U- 238) Cesium 30 years 0.662 MeV 13.07 Nuclear (fission product of U- 235, produced by neutron bombardment) Cobalt 5.26 years 1.17 MeV, 1.33 MeV (avg. 1.25 MeV) 3.26 Nuclear (neutron bombardment of Co-59) Decay Product Pb-206 Ba-137 Ni-60

Additional Radioisotopes in Brachytherapy: (besides Radium-226, Cobalt-60 and Cesium-137) Radioisotope Halflife Ir-192 73.8 Au-198 2.7 I-125 59.4 Pd-103 17 Sr-90-Y-90 28.9 years Energy 0.38 MeV Exposure Production rate constant (R cm 2 h - 1 Ci -1 ) 4.69 In nuclear (neutron bombardment of Ir-191) Decay product Pt-192 Applications LDR-ISRT, HDR-ICRT, ISRT, intravascular brachytherapy β _ Ocular plaque Additional Isotopes in intravascular brachytherapy: Y-90 β W-188-Re188 β P-32 β Re-188 β Ru-106-Rh-106 β V-48 β Developmental Radio-isotopes: Am-241 γ Yb-169 γ Cf-252 neutron Cs-131 γ Sm-145 γ

Radiopharmaceuticals in Internal Therapeutic Use: Radiopharmaceutical Halflife Emissio n Applications I-131 Sodium iodide 8 (1) Treatment of hyperthyroidism (2) Definitive treatment & palliation of Ca.thyroid P-32 Sodium phosphate P-32 Chromium phosphate 14.3 14.3 Sm-153-EDTMP 1.9 Sr-89 Strontium 50.5 chloride Re-186 Renium HDP 3.8 β β Treatment of myeloproliferative disorders (Primary Polycythemia Vera & Thrombocytosis) Intracavitary treatment of malignant effusions Administration Oral(30 mci) Oral(150-250 mci) (<5mCi) Intra-pleural /intrapertitoneal (10-20 mci) Desirable characteristics of therapeutic nonsealed radioisotopes: (1) High LET (best to use β or α-emitters or radionuclides that decay by electron capture and internal conversion to emit X-rays) (2) Short effective half-life (in ) (3) High target-nontarget ratio (4) Deliver minimal radiation dose to medical personnel (5) Readilty available at reasonable cost Side effects: (1) Sr-90, Sm-153, Re-186, P-32 () Bone marrow depression (especially thrombocytopenia) (2) P-32 (intra-peritoneal) N+V, diarrhea, pain abdomen, bowel obstruction (3) I-131 Thyroiditis, oesophagitis, gastritis, sialoadenitis, xerostomia. Radioisotopes in Radioimmunotherapy: In radioimmunotherapy. Radioisotopes (usually beta emitters) are conjugated with monoclonal antibodies. The MAbs home to cells expressing the relevant antigens while the bystander cells which do not express MAbs can also be killed by the beta-rays emitted by the radioisotopes (as cross-fire effect). Mainly used in relapsed and refractory

hematopoietic malignancies. May be used as pre-targetted radioimmunotherapy, where a radiopharmaceutical is first administered and allowed to concentrate in the diseased tissue and then an activating substance is administered to activate cell kill which is localized to the target organ/ tissue. Radioimmunoglobuli n Ibritumomab tiuxetan (Zevalin) Tositumomab (Bexxar) Radioisotope MAb Applications I-131 Anti-CD 20 Relapsed and refractory lowgrade Y-90 Anti-CD 20 NHL Non-sealed radio-isotopes: Precautions: It is mandatory to check that female patients are not pregnant. If administration is to be done, it should be ensured that line is freeflowing Proper guidelines should be followed in preparation, administration and documentation of the radio-isotopes. Proper guidelines should be followed in case of leakage or spillage of unsealed radio-isotopes for evacuation, decontamination and notification. Patients are not be discharged from care until the activity of the remaining radioisotope in their bodies has dropped to below 30 mci and the total effective dose equivalent to any other individual is below 5 msv. While the patient is kept admitted, all body effluents should be properly flushed in the toilet while all trash and nondisposeable items must be stored until radiation levels are normalized. Dosimtery of therapeutic radio-isotopes: (1) Empiric method /fixed administered activity (2) Delivered dose method.