Abstract
The goal of radiopharmaceutical chemistry is to design and develop radiotracers targeted to an organ or function whose activity kinetics in tissue can be detected externally by a gamma or a positron device. Three years ago, Eckelman and Reba (1) divided radiopharmaceuticals into the general categories of specific and non-specific agents. The specific radiopharmaceuticals are the tracers that follow a biochemical pathway or are involved in a particular interaction, for example metabolic substrates, drugs or analogs, and antibodies, Non-specific radiopharmaceuticals include radiolabeled liposomes, cells, microspheres, perfusion agents, inert gases, ethers, alcohols or thallium-201. The design and development of both types of radiopharmaceuticals are important. In the case of myocardial imaging agents, a perfusion agent that will enable differentiation of various stages of ischemia and infarction is as essential as a specific tracer that will reflect metabolism since both perfusion and metabolic functions change with injury.
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Elmaleh, D.R., Livni, E., Levy, S. (1983). Biochemical Considerations in the Design of Radiopharmaceuticals. In: Reba, R.C., Goodenough, D.J., Davidson, H.F. (eds) Diagnostic Imaging in Medicine. NATO ASI Series, vol 61. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-6810-3_14
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