Clinical Nuclear Medicine 2020
DOI: 10.1007/978-3-030-39457-8_2
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Radiopharmaceutical Sciences

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Cited by 5 publications
(10 citation statements)
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References 790 publications
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“…Radioactive iodine (RAI) was the first radiopharmaceutical of clinical importance in nuclear medicine ( 1 ). RAI treatment has been used to treat hyperthyroidism and well-differentiated thyroid carcinoma ( 2 , 3 ), and the basic term “radiotheranostics” has been used in clinical practice since 1940s ( 4 ). RAI treatment remains the main treatment strategy, especially in well-differentiated thyroid cancer of intermediate- and high-risk features.…”
Section: Introductionmentioning
confidence: 99%
“…Radioactive iodine (RAI) was the first radiopharmaceutical of clinical importance in nuclear medicine ( 1 ). RAI treatment has been used to treat hyperthyroidism and well-differentiated thyroid carcinoma ( 2 , 3 ), and the basic term “radiotheranostics” has been used in clinical practice since 1940s ( 4 ). RAI treatment remains the main treatment strategy, especially in well-differentiated thyroid cancer of intermediate- and high-risk features.…”
Section: Introductionmentioning
confidence: 99%
“…The majority of PET imaging preclinical and clinical studies refer to 18 F labeled c(RGD) n multimers, while following them are the 68 Ga and 64 Cu labeled ones. 18 F is a PET radioisotope combining favorable physical and chemical characteristics (half-life = 109 min, β + 96.7%, 0.64 MeV), which can be easily produced as aqueous fluoride by means of proton irradiation of 18 O-enriched water with a biomedical cyclotron [31]. 18 F-radiolabeling is achieved using reactions of nucleophilic substitution on suitable precursors, which carry appropriate leaving groups e.g., halides, sulfonates, and ammonium cations, or aromatic rings with activating residues like electron-withdrawing groups in appropriate positions [32].…”
Section: F Labeled Cyclic Rgd Multimersmentioning
confidence: 99%
“…The introduction of chelator groups i.e., NOTA, DOTA (1,4,7,10-tetraazadodecane-N,N,N,N-tetraacetic acid), facilitates the radiolabeling of c(RGD) multimers with various radionuclides; among them the positron-emitting PET radionuclide 64 Cu (half-life = 762 min, β + 17.9%, 0.64 MeV), which can be produced from a biomedical cyclotron with various methods [31]. Radiolabeling is achieved by complexation of 64 (Figure 8) [56].…”
Section: Cu Labeled C(rgd) Multimersmentioning
confidence: 99%
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“…A cyclotron is a specialized, large-scale device (14,15) in which charged particles such as protons, deuterons or alpha particles can be accelerated to very high speeds in a circular path and directed on predominantly liquid and solid targets consisting of stable (enriched) isotopes converted into corresponding radionuclides by nuclear reactions (see Figure 1). The result is radioactive atoms that can be separated from the target material and radiochemically processed in synthesis modules (radiosynthesizers) for the automated production of tracers, which are formulated mainly into saline PET radiopharmaceutical injection solutions to image patients by intravenous injection of the radiopharmaceutical (15,16). Common short-lived radionuclides used for PET imaging include e.g., 18 F, 68 Ga, 11 C, 13 N, 15 O, 44 Sc, 64 Cu, 89 Zr, 86 Y and 124 I (9,(17)(18)(19)(20)(21).…”
Section: Introductionmentioning
confidence: 99%