“…They can all be produced at low-energy cyclotrons. Besides those four positron emitters, two other short-lived positron emitters, namely 68 15 O, in a few PET centres a small single particle cyclotron (E d < 4 MeV) has also been successfully utilized.…”
Section: Positron Emitters For Petmentioning
confidence: 99%
“…The product 123 Xe is removed from the NaI target, collected in a vessel and is allowed to decay for about 7 h. Thereafter 123 I is collected in a small volume by rinsing the inner wall of the vessel. This process leads to a high yield of 123 The above mentioned two less commonly used SPECT radionuclides, namely 67 Ga and 111 In, which are now also considered for Auger therapy (see below) are produced at a medium-sized cyclotron over the optimum energy range of E p = 25 → 18 MeV via the nuclear reactions 68 Zn( p, 2n) 67 Ga and 112 Cd( p, 2n) 111 In, respectively [cf . 4].…”
Section: Gamma Emitters For Spectmentioning
confidence: 99%
“…15]. The radionuclide 68 Ge is basically produced via the 69 Ga( p, 2n) 68 Ge reaction since the cross section is rather high (see discussion below). However, due to its long half-life, the yield is low and high proton beam fluxes approaching the mA level are essential.…”
Section: Positron Emitters For Petmentioning
confidence: 99%
“…As mentioned above, the production of the parent nuclides of the two commonly used generator-produced β + emitters, namely 68 Ga and 82 Rb, is done using intermediate energy reactions [cf . 15].…”
Section: Positron Emitters For Petmentioning
confidence: 99%
“…They comprise novel positron emitters and therapeutic radionuclides emitting low-range electrons and α-particles. The possible alternative production routes of a few established radionuclides, like 68 Ga and 99m Tc, are discussed. The status of standardisation of production data of the commonly used as well as of some emerging radionuclides is briefly mentioned.…”
Reactor and cyclotron production of medical radionuclides / γ -ray emitters for SPECT / Positron emitters for PET / Corpuscular radiation emitters for internal radiotherapy / Low and intermediate energy nuclear reactions / Radionuclide generators / Future directionsSummary. Medical radionuclide production technology is well established. Both reactors and cyclotrons are utilized for production; the positron emitters, however, are produced exclusively using cyclotrons. A brief survey of the production methods of most commonly used diagnostic and therapeutic radionuclides is given. The emerging radionuclides are considered in more detail. They comprise novel positron emitters and therapeutic radionuclides emitting low-range electrons and α-particles. The possible alternative production routes of a few established radionuclides, like 68 Ga and 99m Tc, are discussed. The status of standardisation of production data of the commonly used as well as of some emerging radionuclides is briefly mentioned. Some notions on anticipated future trends in the production and application of radionuclides are considered.
“…They can all be produced at low-energy cyclotrons. Besides those four positron emitters, two other short-lived positron emitters, namely 68 15 O, in a few PET centres a small single particle cyclotron (E d < 4 MeV) has also been successfully utilized.…”
Section: Positron Emitters For Petmentioning
confidence: 99%
“…The product 123 Xe is removed from the NaI target, collected in a vessel and is allowed to decay for about 7 h. Thereafter 123 I is collected in a small volume by rinsing the inner wall of the vessel. This process leads to a high yield of 123 The above mentioned two less commonly used SPECT radionuclides, namely 67 Ga and 111 In, which are now also considered for Auger therapy (see below) are produced at a medium-sized cyclotron over the optimum energy range of E p = 25 → 18 MeV via the nuclear reactions 68 Zn( p, 2n) 67 Ga and 112 Cd( p, 2n) 111 In, respectively [cf . 4].…”
Section: Gamma Emitters For Spectmentioning
confidence: 99%
“…15]. The radionuclide 68 Ge is basically produced via the 69 Ga( p, 2n) 68 Ge reaction since the cross section is rather high (see discussion below). However, due to its long half-life, the yield is low and high proton beam fluxes approaching the mA level are essential.…”
Section: Positron Emitters For Petmentioning
confidence: 99%
“…As mentioned above, the production of the parent nuclides of the two commonly used generator-produced β + emitters, namely 68 Ga and 82 Rb, is done using intermediate energy reactions [cf . 15].…”
Section: Positron Emitters For Petmentioning
confidence: 99%
“…They comprise novel positron emitters and therapeutic radionuclides emitting low-range electrons and α-particles. The possible alternative production routes of a few established radionuclides, like 68 Ga and 99m Tc, are discussed. The status of standardisation of production data of the commonly used as well as of some emerging radionuclides is briefly mentioned.…”
Reactor and cyclotron production of medical radionuclides / γ -ray emitters for SPECT / Positron emitters for PET / Corpuscular radiation emitters for internal radiotherapy / Low and intermediate energy nuclear reactions / Radionuclide generators / Future directionsSummary. Medical radionuclide production technology is well established. Both reactors and cyclotrons are utilized for production; the positron emitters, however, are produced exclusively using cyclotrons. A brief survey of the production methods of most commonly used diagnostic and therapeutic radionuclides is given. The emerging radionuclides are considered in more detail. They comprise novel positron emitters and therapeutic radionuclides emitting low-range electrons and α-particles. The possible alternative production routes of a few established radionuclides, like 68 Ga and 99m Tc, are discussed. The status of standardisation of production data of the commonly used as well as of some emerging radionuclides is briefly mentioned. Some notions on anticipated future trends in the production and application of radionuclides are considered.
Two macrocyclic ligands based on cyclam with trans-disposed N-methyl and N-(4-aminobenzyl) substituents as well as two methylphosphinic (H2L1) or methylphosphonic (H4L2) acid pendant arms were synthesised and investigated in solution. The ligands form stable complexes with transition metal ions. Both ligands show high thermodynamic selectivity for divalent copper over nickel(II) and zinc(II)-K(CuL) is larger than K(Ni/ZnL) by about seven orders of magnitude. Complexation is significantly faster for the phosphonate ligand H4L2, probably due to the stronger coordination ability of the more basic phosphonate groups, which efficiently bind the metal ion in an "out-of-cage" complex and thus accelerate its "in-cage" binding. The rate of Cu(II) complexation by the phosphinate ligand H2L1 is comparable to that of cyclam itself and its derivatives with non-coordinating substituents. Acid-assisted decomplexation of the copper(II) complexes is relatively fast (τ1/2 = 44 and 42 s in 1 M aq. HClO4 at 25 °C for H2L1 and H4L2, respectively). This combination of properties is convenient for selective copper removal/purification. Thus, the title ligands were employed in the preparation of ion-selective resins for radiocopper(II) separation. Glycidyl methacrylate copolymer beads were modified with the ligands through a diazotisation reaction. The separation ability of the modified polymers was tested with cold copper(II) and non-carrier-added (64)Cu in the presence of a large excess of both nickel(II) and zinc(II). The experiments exhibited high overall separation efficiency leading to 60-70% recovery of radiocopper with high selectivity over the other metal ions, which were originally present in 900-fold molar excess. The results showed that chelating resins with properly tuned selectivity of their complexing moieties can be employed for radiocopper separation.
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