INTERMETALLIC COMPOUNDS OF COBALT AS TARGETS FOR THE PRODUCTION OF THERANOSTIC RADIONUCLIDES

Abstract

Cobalt intermetallic compounds that include cobalt and a second element are provided. The isotopes of the second element in the compounds are present in their natural isotopic abundance or in an enriched isotopic abundance. Methods of making the compounds and methods of using the compounds as targets in the production of radionuclides are further provided.

Claims

1. A method of generating radionuclides from a target comprising a cobalt intermetallic compound comprising cobalt and a second element, wherein the second element is selected from the group consisting of selenium, tellurium, chromium, calcium, titanium, rubidium, and sulfur, the method comprising: bombarding the cobalt intermetallic compound with particles having energies that are sufficiently high to induce a nuclear reaction that produces the radionuclides from the cobalt intermetallic compound; and isolating the radionuclides from the bombarded cobalt intermetallic compound.

2. The method of claim 1, wherein the second element in the cobalt intermetallic compound is isotopically enriched.

3. The method of claim 1, wherein the cobalt intermetallic compound is bombarded with the particles in a proton accelerator.

4. The method of claim 1, wherein the cobalt intermetallic compound is bombarded with the particles in a cyclotron.

5. The method of claim 1, wherein the second element is selenium.

6. The method of claim 5, wherein the particles are protons and the cobalt intermetallic compound is bombarded with the protons in a cyclotron.

7. The method of claim 5, wherein the abundance of .sup.76Se, .sup.77Se, or .sup.80Se in the cobalt intermetallic compound is enriched relative to its natural abundance.

8. The method of claim 5, wherein the radionuclide is a radionuclide of bromine.

9. The method of claim 8, wherein, after isolating the radionuclides from the bombarded cobalt intermetallic compound, the target is reused by bombarding the cobalt intermetallic compound with more particles having energies that are sufficiently high to induce a nuclear reaction to produce more of the radionuclides.

10. The method of claim 8, wherein the cobalt intermetallic compound comprises Co.sup.76Se, Co.sup.77Se, or Co.sup.80Se and the radionuclide comprises .sup.76Br, .sup.77Br, or .sup.80mBr.

11. The method of claim 5, wherein the radionuclide is a radionuclide of arsenic.

12. The method of claim 11, wherein the cobalt intermetallic compound comprises Co.sup.74Se, Co.sup.77Se, or Co.sup.80Se and the radionuclide comprises .sup.71As, .sup.74As, or .sup.77As.

13. The method of claim 1, wherein the target further comprises a target backing and the method further comprises forming the target by pre-synthesizing the cobalt intermetallic compound and subsequently contacting the pre-synthesized cobalt intermetallic compound with the target backing.

14. The method of claim 13, wherein the target backing does not comprise cobalt.

15. The method of claim 13, wherein the target backing comprises niobium, nickel, copper, or aluminum.

16. The method of claim 1, wherein isolating the radionuclides from the bombarded cobalt intermetallic compound is carried out using dry distillation or column extraction chromatography.

17. The method of claim 1, further comprising synthesizing the cobalt intermetallic compound by reacting a cobalt powder with a powder of the second element.

18. The method of claim 1, wherein the second element is tellurium, chromium, calcium, titanium, rubidium, or sulfur.

19. A method of forming radiopharmaceutical compounds, the method comprising generating radionuclides using the method of claim 1 and labeling pharmaceutical compounds with the radionuclides.

20. A method of generating short-lived radionuclides, the method comprising generating radionuclides using the method of claim 1, allowing the radionuclides generated from the method of claim 1 to decay into short-lived radionuclides, and separating the short-lived radionuclides from the radionuclides generated from the method of claim 1.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0012] Illustrative embodiments of the invention will hereafter be described with reference to the accompanying drawings, wherein like numerals denote like elements.

[0013] FIG. 1 depicts a radiobromine furnace assembly with (102) Ar gas inlet, (104) 14 cm outer flat-bottomed quartz tube for Ar inlet, (106) CoSe target disc, (108) 24 cm inner bell-bottomed quartz tube for Ar outlet, (110) furnace assembly outlet compression fitting, (112) 3-way Hamilton valve, (114) PTFE line through ice-water bath, (116) initial H.sub.2O bubble trap, and (118) scrubber assembly with empty, H.sub.2O, and 1 mM Na.sub.2S.sub.2O.sub.5 tubes, respectively.

[0014] FIG. 2 depicts radiosynthesis of a .sup.77Br-labeled PARP-1 inhibitor.

[0015] FIG. 3 depicts bromine-80m production yield from 16.1 MeV proton irradiation of Co.sup.80Se at various intensities, reported both as end of saturated bombardment (EoSB, MBq/A) and physical (MBq/(A.Math.h)) yields. (Otuka, N. et al., 2015. Radiochim. Acta, 103(1), 1-6.)

[0016] FIG. 4 depicts cyclotron production yield of .sup.80mBr, .sup.77Br, and .sup.76Br from irradiation of Co.sup.80Se, Co.sup.77Se, and Co.sup.76Se, respectively, at various proton energies. Error bars represent standard deviations of results from multiple irradiations.

[0017] FIG. 5 (graph regions (a)-(d)) depicts typical radiation profiles in kilocounts per second (kCPS) of radiation detectors in a radiobromine distillation apparatus. Detector collimated on CoSe (106) is shown in black on the left y-axis while detector collimated on the initial H.sub.2O trap (116) is shown in grey on the right y-axis. FIG. 5, graph region (a) is during furnace distillation; FIG. 5, graph region (b) is during the quench/cooling period; FIG. 5, graph region (c) is during the H.sub.2O rinse of outlet quartz and PTFE lines; and FIG. 5, graph region (d) is during the quaternary methyl amine anion exchange cartridge loading.

DETAILED DESCRIPTION

[0018] Cobalt intermetallic compounds, methods for making the intermetallic compounds, and methods for using the intermetallic compounds as targets in the production of radionuclides are provided. Various embodiments of the methods are able to produce radionuclides in quantities and purities that make large scale production, distribution, and clinical application possible using low and medium energy proton accelerators.

[0019] The intermetallic compounds include cobalt and a second element, wherein the second element is of natural or enriched isotopic abundance. As used herein, the terms enriched isotopic abundance and isotopically enriched mean that the relative abundance of at least one isotope of the element has been enriched relative to the natural abundance of that isotope in that element. For example, selenium that is isotopically enriched in its 76-isotope, relative to the abundance of the 76-isotope in naturally occurring selenium, is designated .sup.76Se. In some instances, the isotopically enriched element consists of only the enriched isotope of that element. Elements having a natural isotopic abundance are designated herein as nat; for example, selenium having a natural isotopic abundance is designated as .sup.natSe.

[0020] Elements that may be included in the cobalt intermetallic compounds include elements that are capable of forming stoichiometrically stable intermetallic compounds with melting points higher than those of the pure element in the absence of cobalt, and capable of wetting thermally conductive metal substrates that are used for incorporation into common irradiation geometries. These elements include the metalloids selenium and tellurium, the metals gallium, chromium, calcium, titanium, germanium, and rubidium, and the nonmetal sulfur.

[0021] The intermetallic compounds can be synthesized by heating a stoichiometric mixture of cobalt powder and a powder of the isotopically enriched second element in an inert environment for a time sufficient for intermetallic compound formation. The intermetallic compounds can then be formed into cyclotron targets by hot pressing onto a target backing in a furnace followed by rapid cooling. The target backing may be composed of a variety of materials, provided it is highly thermally conductive, and may be water-cooled in order to cool the intermetallic compound target material during proton bombardment. Suitable target backing materials include niobium, cobalt, nickel, copper, and aluminum.

[0022] When the intermetallic compounds are bombarded with energetic bombarding particles, nuclear reactions form radionuclides, which can be radiochemically isolated for a variety of applications. The choice of bombarding particle and irradiation parameters will depend on the specific target material being used, the desired radionuclides, and the radionuclide yield and purity requirements. Suitable bombarding particles include charged particles (e.g., protons) and neutral particles (e.g., neutrons). The reactions can be carried out in a cyclotron. However, other particle accelerators, including linear accelerators, can be used. For some target materials and radionuclides, relatively low energy protons can be used, including protons having energies of about 30 MeV or lower. By way of illustration, low energy cyclotrons commonly utilize protons having energies in the range from about 10 MeV to 24 MeV. However, higher or lower proton energies can be used.

[0023] As one of ordinary skill in the art will understand, the radionuclides produced by a given target compound will depend on the stable isotopes present in the target compound, the beam energy, and the resulting nuclear reactions. Many of the radionuclides produced from the cobalt compounds described herein are produced via a (p,n) nuclear reaction. However, others are produced by different nuclear reactions, including (p,xn) (e.g., x=2, x=3, etc) and (p,alpha) reactions. The cobalt compounds can be used to produce short-lived radionuclides. These radionuclides have short half-lives, typically on the order of minutes to hours, so that their radioactivity rapidly decreases to a safe level after use. These short-lived radionuclides are typically used immediately after production to synthesize radiopharmaceuticals emitting -rays, positrons, or electrons. Other radionuclides produced from the cobalt intermetallic compounds are generator radionuclides. These are longer-lived parent radionuclides from which a different short-lived radionuclide is formed continually as a result of decay. The short-lived radionuclide can be periodically separated from the generator radionuclide for use in a diagnostic or therapeutic application. The isotope pairs .sup.68Ge/.sup.68Ga and .sup.82Sr/.sup.82Rb are examples of radionuclide generators and their short-lived products.

[0024] If the radionuclides being produced and collected are sufficiently volatile, a thermochromatographic dry distillation can be used to isolate the radionuclides from the irradiated target materials by evaporation at high temperature. This can be carried out by transferring the irradiated targets to a furnace under an inert environment, heating the irradiated target materials to release the radionuclides, and collecting the released radionuclides for use. Alternatively, for less volatile radionuclides, isolation can be carried out using column extraction chromatography with an extraction resin.

[0025] Once formed, the radionuclides can be used to label small amounts of a pharmaceutical compound of interest, creating radiopharmaceuticals. Positron emitting radionuclides can be used to label a variety of different compounds, allowing the study of biological systems using positron emission tomography (PET) imaging.

[0026] One illustrative embodiment of a method for producing radionuclides uses cobalt selenide (CoSe) intermetallic compounds as targets for the production of theranostic bromine radionuclides. For example, CoSe intermetallic compounds containing 50 to 60 mol % Se can be used. Using the method, high purity .sup.77Br, .sup.76Br, and .sup.80mBr radionuclides can be generated by the irradiation of Co.sup.77Se or Co.sup.78Se, Co.sup.76Se, and Co.sup.80Se intermetallic compound targets, respectively. A detailed description of this method is provided in Example 1. The use of CoSe targets mitigates the thermal and dosimetric limitations of other radiobromine production targets because the CoSe intermetallic compounds are able to tolerate higher intensity proton irradiations and produce more radiobromine than has previously been reported. Moreover, CoSe targets have the advantage of releasing radiobromine that can be recovered efficiently using a dry distillation process in a vertical distillation assembly, allowing for a simplified radiochemical isolation and the reuse of the isotopically enriched CoSe target for many subsequent productions of the radionuclides. The use of a vertical dry distillation assembly offers several key advantages over horizontal assemblies, including better hot cell compatibility, more rapid heating, and quench cooling of CoSe targets. Other radionuclides that can be formed via proton bombardment of CoSe targets include: .sup.71As, which can be formed using a Co.sup.74Se target; .sup.74As, which can be formed using a Co.sup.77Se target; and .sup.77As, which can be formed using a Co.sup.80Se target.

[0027] Another illustrative embodiment of a method for producing radionuclides uses cobalt gallium (CoGe) intermetallic compounds as targets for the production of germanium radionuclides. Using the method, high purity .sup.68Ge, .sup.69Ge, and .sup.71Ge radionuclides can be generated by the irradiation of Co.sup.natGa, Co.sup.69Ga, and Co.sup.71Ga compound targets, respectively. A detailed description of methods of making CoGa intermetallic compounds for the production of germanium radionuclides is provided in Example 2. The radionuclide .sup.68Ge can be used as a long-lived parent in a generator device which produces the short-lived radionuclide .sup.68Ga for PET imaging. The .sup.69Ge and .sup.71Ge can be used as a theranostic pair, capable of both imaging and treatment of human disease.

[0028] Yet another illustrative embodiment of a method for producing radionuclides uses cobalt telluride (CoTe) intermetallic compounds as targets for the production of iodine radionuclides. Using the method, high purity .sup.124I and .sup.123I radionuclides can be generated by the irradiation of Co.sup.124Te and Co.sup.123Te intermetallic compound targets, respectively. The radionuclides .sup.123I can be used in SPECT and Auger therapy and .sup.124I can be used in PET imaging in diagnostic and therapeutic applications.

[0029] Other cobalt intermetallic compounds that can be used to form radionuclides include: Co.sup.52Cr compounds (25-45 mol % Co), which can be used as targets for the production of .sup.52gMn; Co.sup.42,43,44,46,48Ca compounds (85-95 mol % Co), which can be used as targets for the production of .sup.43Sc, .sup.44Sc, and .sup.47Sc; Co.sup.46,47,50Ti compounds (45-55 mol % Co), which can be used as targets for the production of .sup.43Sc, .sup.44Sc, and .sup.47Sc; Co.sup.70,72,74Ge compounds (50-70 mol % Co), which can be used as targets in the production of .sup.71As, .sup.72As, and .sup.74As; Co.sup.34S compounds (40-60 mol % Co), which can be used as targets in the production of .sup.34mCl; and CoRb compounds (40-60 mol % Co), which can be used as targets in the production of .sup.82Sr/.sup.82Rb generators. These cobalt compounds can be synthesized using the procedures outlined in Examples 1 and 2 with the corresponding elemental starting powders. The mole percent ranges listed above are illustrative ranges for the cobalt content of the intermetallic compounds; however, percentages outside of these ranges can be used.

EXAMPLES

Example 1: Production of Bromine Radionuclides from Cobalt Selenide Intermetallic Compounds

[0030] This example describes a method by which high radionuclidic purity .sup.76Br, .sup.77Br, and .sup.80mBr are each produced via the proton irradiation of Co.sup.76/77/80Se targets. Cyclotron production yields were 10310 MBq/(A.Math.h) for .sup.76Br, 8810 MBq/(A.Math.h) for .sup.80mBr at 16 MeV, and 171 MBq/(A.Math.h) for .sup.77Br at 13 MeV. Optimized dry distillation radiobromine recovery was 7611% in a small volume of aqueous solution. A .sup.77Br-labeled radiopharmaceutical with apparent molar activity up to 700 GBq/umole was synthesized via copper-mediated aryl boronic ester bromination.

Materials and Methods

[0031] Cobalt powder (Alfa Aesar, 1.6 m, 99.8%), natural enrichment selenium powder (Acros Organics, 200 mesh, 99.5%), and isotopically enriched selenium powders (Isoflex USA) of isotopic abundance summarized in Table 1 were used for the synthesis of the intermetallic CoSe. Fused quartz tubing (QSI Scientific, Inc) was used for the in-house fabrication of vacuum ampules and furnace assembly parts. Boron nitride (Alfa Aesar) was machined for furnace assembly parts, cleaned with ethanol and baked at 1000 C. prior to use. 1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-8,9-dihydro-2,7,9a-triazabenzo[cd]azulen-6(7H)-one (pre-KX1-Bpin) and 1-(4-iodophenyl)-8,9-dihydro-2,7,9a-triazabenzo[cd]azulen-6(7H)-one (KX-1) were synthesized at the University of Pennsylvania as previously described. (Reilly, S. W. et al., 2018, Org. Lett. 20, 1752-1755.) Copper catalyst (tetrakis(pyridine)copper (II) triflate; Cu(py).sub.4(OTf).sub.2) and ligand (3,4,7,8-tetramethyl-1,10-phenanthroline; Lig) were obtained from Sigma Aldrich. Sep-Pak QMA Plus Light (Waters, QMA light) cartridges were prepared with 1 mL of 1 M KHCO.sub.3 and 10 mL water, and Sep-Pak C18 Plus light (Waters, C18 light) cartridges were prepared with 5 mL ethanol and 10 mL water prior to use. All other chemicals were purchased from Sigma Aldrich and used as received.

TABLE-US-00001 TABLE 1 Isotopic abundances of enriched selenium target material. Isotopic composition (%) .sup.74Se .sup.76Se .sup.77Se .sup.78Se .sup.80Se .sup.82Se .sup.76Se <0.05 99.8 0.1 0.2 0.1 <0.05 <0.05 <0.05 .sup.77Se 0.02 0.14 99.66 0.09 0.05 0.04 .sup.80Se 0.01 0.03 0.02 0.01 99.9 0.02

[0032] Preparation of cobalt selenide target material.

[0033] Cobalt selenide was formed by weighing an equal molar ratio of cobalt (110-130 mg) and selenium (150-170 mg) into a quartz test tube. The tube was flushed by repeated evacuation to <100 Pa and back filling with argon and scaled under vacuum. Over 100 minutes, the upright tube was heated from room temperature to 1200 C. where it was held for one hour, then removed from the furnace and rapidly cooled by immersing in water.

Preparation and Characterization of CoSe Cyclotron Targets

[0034] CoSe cyclotron targets were formed by hot pressing CoSe into a pocketed (=9.5 mm, 1 mm deep) niobium disc (=19 mm, 2 mm thick) using the vertical furnace assembly shown in FIG. 1. The Nb disc, a 250 mg CoSe pellet, and a boron nitride (BN) tamper were placed at the bottom of the flat-bottomed quartz tube (104) and flushed with argon through the assembly gas inlet (102). The tube was then lowered into a preheated vertical tube furnace (107) at 1075-1100 C. for 5 minutes and flattened by loosening the outlet compression fitting (110) and applying <0.1 MPa of pressure to the BN tamper with the bell-bottomed inner quartz tube (108). The CoSe target was rapidly cooled by lifting the assembly from inside the furnace and immediately immersing in water. This process was repeated using BN tampers of various configurations until CoSe was uniform and well adhered in the pocket of the niobium disc. CoSe that wetted face of the niobium disc outside the pocket was removed using a razor blade and reclaimed. The face of the niobium disc was then polished using fine grit sandpaper, creating a suitable surface for an o-ring seal. A prepared Nb-backed CoSe cyclotron target was analyzed by X-ray diffraction using a Bruker D8 Discovery X-ray Diffractometer with a Cu K (1.54 ) X-ray source and a Vantec-500 detector. Diffraction data was acquired using a 2 mm cone diameter and 0.6 per min sample rotations.

Cyclotron Irradiation of CoSe Targets

[0035] Cyclotron irradiations with 0.25-2.5 hour durations of Co.sup.natSe, Co.sup.80Se, Co.sup.76Se, and Co.sup.77Se targets with 5-40 A of 11-16 MeV orthogonally incident protons were performed using the University of Wisconsin GE PETtrace cyclotron. CoSe targets were cooled with a water-jet directly to the back of the Nb disc using an ARTMS QIS solid target system. The radiobromine production yield and radionuclidic purity at the end of bombardment (EoB) was investigated at four proton energies by employing a water-cooled degrader foil positioned 3.6 cm away from the face of the CoSe target. Molybdenum and tungsten foils (Alfa Acsar) were used as proton energy degrader foils with a 0.25 mm Mo foil degrading the 16 MeV primary beam to 11 MeV, a 0.20 mm Mo foil degrading to 12 MeV, and a 0.10 mm W foil degrading to 13 MeV, based on calculations performed with SRIM-2013.00. (Ziegler et al., 2010. Nucl. Inst. Meth. Phys. Res. B 268(11-12), 1818-1823.) The radioactivity in the CoSe target was directly estimated by high purity germanium (HPGe) spectrometry or dose calibrator measurements of fractions following radiochemical separation.

Dry Distillation of Radiobromine from CoSe Targets

[0036] Radiobromine was isolated from irradiated CoSe targets by thermal chromatographic distillation using the furnace assembly shown in FIG. 1. Following irradiation, the Nb-backed CoSe was removed from the QIS transfer capsule, dried, placed in the flat-bottomed quartz tube (104), sealed inside the assembly, and flushed with 50 mL/min argon flow. The sealed, argon-flushed quartz tube (104) was then lowered into the tube furnace preheated to 1050 C. Collimated detectors monitored the radioactivity in the CoSe target (106) and the initial H.sub.2O trap (116). After 5-15 minutes of heating, the quartz tube (104) was lifted from the furnace and immediately immersed in water, rapidly cooling the CoSe target. Argon flow continued while the assembly thermally cooled for 5-10 minutes. After cooling, the assembly was allowed to come to atmospheric pressure, and through manipulation of the 3-way valve (112), in five aliquots, a total of 1-10 mL of warm water was used to rinse the top 4 cm of the quartz outlet tube and the PTFE outlet line (114) (in ice bath 115) into the initial H.sub.2O trap (116) and scrubber assembly (118) with empty, H.sub.2O, and 1 mM Na.sub.2S.sub.2O.sub.5 tubes. The collected water solution was passed through a prepared QMA light cartridge, trapping the radiobromide, which was then eluted with 700 L of 20 mM K.sub.2SO.sub.4 in 1:1::MeCN:H.sub.2O. Radiochemical yield of the distillation process was assessed by HPGe spectrometry and dose calibrator measurements.

Radiochemical Labeling using .sup.77Br Product

[0037] The radiochemical quality of the [.sup.77Br]bromide in 20 mM K.sub.2SO.sub.4 was evaluated by copper-mediated aryl boronic ester bromination, synthesizing a novel .sup.77Br-labeled analogue of the DNA damage response protein, poly ADP ribose polymerase 1 (PARP-1) inhibitor, rucaparib. The radiochemical reaction, shown in FIG. 2, was investigated by using 1 mole pre-KX1-Bpin with varying solvent volume and composition, K.sub.2SO.sub.4 load, and temperature. Reactions were monitored by autoradiography visualized thin layer chromatography (radioTLC) on silica gel plates with 3:1::ethyl acetate:acetonitrile as mobile phase. The reactions were purified by diluting in 15 mL water, loading on a prepared C18 light cartridge, rinsing with 10 mL water, and eluting crude product in 700 L ethanol. Following a 1:1 dilution with water, the product was purified by preparative HPLC (Kinetix XB-C18, 5 m, 100 , 10250 mm, 4 mL/min 40:60::MeCN:0.1 M ammonium formate, pH 4.5), followed by a final C18 light cartridge purification to obtain the product in a small volume of ethanol solution. Radiochemical conversion was determined by dose calibrator measurement of purified fractions. Stable iodinated KX1 was used as a standard to estimate the mass/254 nm absorbance calibration curve for the .sup.77Br-labeled compound.

Results and Discussion

Preparation and Characterization of Cobalt Selenide Target Material

[0038] Elemental cobalt and selenium powder readily fused into solid pieces (27020 mg) following heating at 1200 C. for 1 hour inside a vacuum ampule. Typical mass losses to the ampule walls were 64% (n=10). Examination of the CoSe binary phase diagram shows that there exists an intermetallic species with stoichiometric flexibility near Co.sub.0.88Se with a melting point of 1078 C. (Okamoto, 1990. Binary Intermetallic compound Phase Diagrams vol. 2, Second Edition, ASM International, Materials Park, Ohio, pp. 1235-1237.)

Preparation and Characterization of CoSe Cyclotron Targets

[0039] The stepwise process of CoSe cyclotron target formation resulted in 6010% of initial CoSe melting into the Nb pocket, with 224% of CoSe reclaimed as powder and a loss of 164% CoSe (n=2). The bulk of this loss was during the scraping and sanding of CoSe that overflowed the pocket in the target disc.

[0040] The CoSe cyclotron targets contained 180-220 mg of CoSe in a 9.5 mm diameter pocket. Calculations using SRIM estimate that this CoSe thickness would degrade 16 MeV incident protons to 10 MeV, 13 MeV protons to 5 MeV, 12 MeV protons to 3 MeV, and stop 11 MeV protons. (Ziegler et al., 2010.) Thus, while the targets were sufficiently thick to effectively maximize the production yield of (p,n) nuclear reactions from 13, 12, and 11 MeV protons, they were too thin to maximize production with 16 MeV protons.

[0041] The X-ray diffraction data taken on Nb-backed CoSe targets included peaks at 33.26, 44.87, 61.66, 69.68, and 82.26, in good agreement with the International Centre for Diffraction Data (ICDD) Powder Diffraction File (PDF) number 04-006-8806 for hexagonal Co.sub.0.85Se. (Zhan et al., 2000. Solid State Chem. 152, 537-539.) These data indicate the successful formation of the desired CoSe intermetallic species using these high-temperature synthesis and hot pressing methods.

Cyclotron Irradiation of CoSe Targets

[0042] Water-cooled CoSe cyclotron targets tolerated proton irradiation extremely well at all investigated proton energies (11-16 MeV) and intensities (5-40 A). No visual changes in appearance were observed to CoSe targets following irradiation, and no mass loss was measured after irradiation. Several factors likely contributed to the exceptional performance of these targets. First, hot pressing provided excellent wetting and thermal contact between the CoSe target material and the niobium backing. Second, the direct water-jet cooling of the niobium backing allowed for very effective removal of the hundreds of watts of proton beam power deposited in the irradiation target.

[0043] Radiobromine yield from a Co.sup.80Se target was investigated as a function of 16.1 MeV proton irradiation intensity (see FIG. 3). The .sup.80mBr production rate was similar between 10 and 40 A, indicating that the CoSe intermetallic target robustly retains radiobromine up to 640 watts of power deposition (at 40 A).

[0044] Targets of Co.sup.natSe, Co.sup.80Se, Co.sup.77Se, and Co.sup.76Se were irradiated with 5-40 A of 11-16 MeV protons (Table 2 and FIG. 4). As shown in Table 3, the isotopically enriched target material allowed for the production of .sup.77Br, .sup.76Br, and .sup.80mBr with excellent radionuclidic purity with the exception of .sup.77Br produced at 16.1 MeV, where the higher energy formed .sup.76Br via the .sup.77Se(p,2n).sup.76Br nuclear reaction. The production of high radionuclidically purity .sup.77Br was observed at proton energies of 13 MeV or less. Minimal proton energy dependent production of .sup.58Co was observed with 0.140.05 MBq/(A.Math.h) at 16 MeV (n=4) and 0.020.01 MBq/(A.Math.h) at 13 MeV (n=3).

TABLE-US-00002 TABLE 2 Cyclotron production yield of .sup.82Br, .sup.80mBr, .sup.76Br, and .sup.77Br from various isotopic compositions of CoSe targets at four proton energies (E.sub.p). Reported uncertainties represent standard deviations of multiple irradiations and estimated when n = 1. Limits of detection calculated from HPGe spectra [Aniin and Yap, 1987] are reported. In some cases (denoted as n/a), HPGe measurements were not performed promptly enough after EoB to quantify short-lived .sup.80mBr. E.sub.p Target Physical yield (MBq/A .Math. h) (MeV) comp. n= .sup.82Br .sup.80mBr .sup.76Br .sup.77Br 16 Co.sup.natSe 4 2.0 0.3 62 7 9.9 0.9 2.8 0.4 Co.sup.80Se 12 0.0011 0.0001 103 10 0.0072 0.0005 0.006 0.005 Co.sup.77Se 1 <0.07 n/a 12 ~1 23 ~2 Co.sup.76Se 2 <0.06 n/a 88 10 0.05 ~0.005 13 Co.sup.80Se 2 0.0015 0.0002 77 7 0.0040 0.0005 <0.002 Co.sup.77Se 3 <0.02 <0.3 0.07 0.01 17 1 Co.sup.76Se 1 <0.004 n/a 50 ~5 0.1 ~0.01 12 Co.sup.77Se 2 <0.002 <0.5 0.048 0.001 13.1 0.5 11 Co.sup.80Se 8 0.0015 0.0003 48 3 0.0010 0.0001 <0.002

TABLE-US-00003 TABLE 3 End of bombardment (EoB) radionuclidic purity of .sup.80mBr, .sup.77Br, and .sup.76Br produced from irradiation of various isotopic compositions of CoSe targets at various proton energies (E.sub.p). E.sub.p Target EoB (MeV) comp. radionuclidic purity 16 Co.sup.80Se 99.99% .sup.80mBr Co.sup.77Se 63% .sup.77Br Co.sup.76Se 99.9% .sup.76Br 13 Co.sup.80Se 99.99% .sup.80mBr Co.sup.77Se 99.6% .sup.77Br Co.sup.76Se 99.8% .sup.76Br 12 Co.sup.77Se 99.6% .sup.77Br 11 Co.sup.80Se 99.99% .sup.80mBr
Dry Distillation of Radiobromine from CoSe Targets

[0045] The isolation of radiobromine from proton irradiated CoSe was readily accomplished by dry distillation at 1050 C. in the vertical furnace assembly shown in FIG. 1. Typical traces of the detectors collimated on the CoSe target (106) and initial H.sub.2O trap (116) are shown in FIG. 5, graph regions (a)-(d). Following the lowering of the assembly into the preheated furnace, radiobromine was distilled from the CoSe in 5-6 minutes. Some non-bromine radioactivity remained in the CoSe target, including .sup.93mMo and .sup.58Co, as shown in FIG. 5, graph region (a). The CoSe was then removed from the furnace in the quartz tube and cooled in water for 10-15 minutes with Ar flow. During cooling (FIG. 5, graph region (b)), the migration of radiobromine was observed through the continuous increase in radiation signal in the H.sub.2O trap detector. After cooling, argon flow was halted, the assembly was allowed to come to atmospheric pressure, and the quartz outlet tube (108) and the PTFE outlet line (114) were rinsed with warm water into the initial H.sub.2O trap (116), moving radiobromine into the H.sub.2O trap (FIG. 5, graph region (c)). After rinsing, the water contained in the H.sub.2O trap was passed through the prepared QMA light cartridge with Ar back pressure (FIG. 5, graph region (d)). Radiobromide was reclaimed from the QMA cartridge by slowly eluting with 700 L of 20 mM K.sub.2SO.sub.4 in 1:1::CH.sub.3CN:H.sub.2O.

[0046] Brassy, black, and red deposits of cobalt and selenium were observed along the quartz outlet tube between the top of the furnace and the level of the Ar gas inlet (102). Additionally, very faint red deposits were visible after distillation in the PTFE outlet line (114) and in the initial H.sub.2O trap (116). Despite this, the loss of macroscopic cobalt and selenium target material was minimal. A Co.sup.77Se target exhibited a total mass loss of 5.3 mg (3% of total Co.sup.77Se target material) after six irradiations (220 A.Math.h total) and four distillations. Additionally, a Co.sup.80Se target seeing 22 irradiations (650 A.Math.h total) and 13 distillations continued to demonstrate no significant change to its .sup.80mBr production yield despite extensive use. The durability of the CoSe targets is likely due to the inherent properties of the CoSe intermetallic species, to the minimal amount of time the targets were heated during distillation, and to the rapid quenching to prevent hot CoSe from partitioning into less resilient cobalt- and selenium-containing species during cool down.

[0047] Radiochemical yield of the dry distillation process was 5525% (n=12) of cyclotron produced radiobromine recovered in a small volume of aqueous solution suitable for radiochemistry. For some distillations, low yield of 3314% (n=6) was attributed to furnace malfunction, QMA cartridge degradation, loose fittings, improper cleaning of quartz outlet tubes, or the accidental inclusion of radiobromine-absorbing rubber tubing. Excluding these results, a radiobromine yield of 7611% (n=6) was observed.

Radiochemical Labeling using .sup.77Br Product

[0048] Following radiochemical isolation by dry distillation, the [.sup.77Br]bromide was used for reaction in a copper-mediated aryl boronic ester bromination to study its radiochemical lability and molar activity. [.sup.77Br] Bromide in 20 mM K.sub.2SO.sub.4, 1:1::MeCN:H.sub.2O was either used directly or following a fast and lossless drying step under argon flow at 120 C. Radiochemical conversions from 4.7-95% were observed for the reaction conditions, as summarized in Table 4. Reaction conditions {1-4} were adapted from work by Reilly et al., and the conditions in {5} were adapted from the work by Zhou et al. (Reilly, S. W. et al., 2018. Org. Lett. 20, 1752-1755 and Zhou, D., et al., 2018. Tetrahedron Letters 59, 1963-1967.) In general, larger reaction volumes and larger water contents negatively affected reactivity, as evidenced by the increase in radiochemical conversion between reactions {2} and {4} from 16% to 26%. Additionally, the use of dimethylsulfoxide (DMSO) as the reaction solvent combined with elevated reaction temperature (80 C.) as in reaction {5} improved radiochemical conversion compared with the similar reaction conditions of {2}, despite lacking the 3,4,7,8-tetramethyl-1,10-phenanthroline as an auxiliary ligand.

[0049] The presence of the K.sub.2SO.sub.4 significantly impeded the bromination reaction, likely as a result of its coordination and deactivation of the tetrakis(pyridine)copper (II) triflate catalyst. Copper sulfate is a poor catalyst in copper-mediated [.sup.18F]fluorination of boronic acids. Comparison of reactions {2} and {4} demonstrates that the hot DMSO conditions proposed by Zhou et al. appear more tolerant to the presence of K.sub.2SO.sub.4. (Zhou et al., 2018.) Potassium sulfate was included in these reactions as it is an effective, non-basic QMA release agent for [.sup.77Br]bromide.

[0050] The collected purified fractions of .sup.77Br-labeled compound were repurified by preparative HPLC to obtain a clean 254 nm absorbance peak coeluting with the radiopeak. Based on absorbance measurements of the iodinated compound, the mass corresponding to .sup.77Br-labeled compound was estimated, yielding an apparent molar activity of 520 GBq/mole (14 Ci/mole) at the time of analysis. This value is 25% of the theoretical maximum .sup.77Br molar activity of 2000 GBq/mole (55 Ci/mole).

TABLE-US-00004 TABLE 4 Radiochemical reaction conditions and radiochemical conversion results of the reaction of [.sup.77Br]bromide in a copper-mediated aryl boronic ester bromination. pre- Reaction solvent KX1- Radiochemical volume Bpin Cu(py).sub.4(OTf).sub.2 Lig K.sub.2SO.sub.4 Temp Time conversion (L) composition (mol) (mol) (mol) (mol) ( C.) (min) (%) {1} 70 11:2:1 ::: 1 0.5 0.5 0.2 20 60 95 MeCN:MeOH:H.sub.2O {2} 110 7.5:1:2.5 ::: 1 0.5 0.5 1 20 90 16 MeCN:MeOH:H.sub.2O {3} 160 10:1:50 ::: 1 0.5 0.5 2 20 110 4.7 MeCN:MeOH:H.sub.2O {4} 65 8:2:1 ::: 1 0.5 0.5 1 20 45 26 MeCN:MeOH:H.sub.2O {5} 140 30:1 :: DMSO:H.sub.2O 1 0.5 0 1.4 80 45 31

Example 2: Production of Germanium Radionuclides from Cobalt Gallium Intermetallic Compounds

[0051] This example describes a method by which high radionuclidic purity .sup.69Ge is produced via the proton irradiation of Co.sup.natGa targets.

[0052] CoGa targets were made by weighing and combining cobalt and gallium masses in round-bottom quartz glass test tubes in atom ratios of Co:Ga 1:2, 1:3, and 1:4. As indicated by their binary phase diagram, these atom ratios were expected to have melting points between 1075 and 925 C., respectively. The combined masses of cobalt and gallium (500 mg each) were flushed with argon gas, evacuated to 10.sup.4 bar using a roughing pump, and then sealed into ampoules with an oxypropane torch. The quartz glass ampoules were then placed in a Thermolyne Model 10500 furnace and heated to a temperature above the indicated melting temperature (1100 C. for 1:2::Co:Ga, 1050 C. for 1:3::Co:Ga, and 950 C. for 1:4::Co:Ga) for about 2 hours before being removed and rapidly quenched to room temperature in a water bath. The ampoules were then breached, and the resulting pellets were weighed to assess the change in mass during forging.

[0053] Pellets with Co:Ga atom ratios 1:3 and 1:4 (n=3 each) were then hot-pressed into niobium crucibles. This was accomplished by placing an empty niobium crucible (19 mm wide, 2 mm deep niobium coin with a centered 9.5 mm OD1 mm deep cavity) in a flat bottom, quartz tube, and then placing a sample pellet in the crucible pocket. Then a boron nitride tamp was placed on top of the pellet and held in place by a quartz glass, bell-ended rod. The quartz tube assembly was sealed with gas adapters, flushed with a continuous nitrogen gas flow, and lowered into the pre-heated, vertical tube furnace cavity. The furnace temperature settings were the same as those listed above for the various atom ratios. After 5 minutes of exposure to the heat of the furnace, the pellet became malleable, and the glass rod was depressed manually to fill the crucible pocket with the sample. Finally, the assembly was removed from the furnace and rapidly quenched to room temperature in a water bath. Both empty crucibles and hot-pressed crucibles were weighed to quantify any mass loss.

[0054] The hot-pressed material and backings were mounted in a cyclotron target holder with a water jet directed onto the back of the target. A 200 m molybdenum containment foil mounted to the front of the target prevented interaction between the target material and cyclotron components. This target holder was in turn mounted on a GE PETtrace 16 MeV (H+) cyclotron and irradiated with beam intensities ranging from 10-35 A for 30-60 minutes. Produced radioactivity and radionuclidic purity was quantified by High Purity Germanium crystal (HPGe) gamma spectrometry of the targets.

[0055] Following irradiation with 13 MeV protons, radiochemical isolation of the germanium isotope was carried out by single column extraction chromatography using an extraction resin functionalized with N,N,N, N-tetrakis-2-ethylhexyldiglycolamide (branched DGA, Eichrom), as described in H. F. Valdovinos (2017), Production, labeling and in vivo studies with the theranostic positron-emitting radiometals .sup.44Sc, .sup.55/58m/58gCo, .sup.61/64Cu, .sup.86Y and .sup.69Gc, PhD Dissertation, University of Wisconsin-Madison, Madison, WI. Irradiated targets were dissolved in 1-2 hours with 5 mL of c. HNO.sub.3. Aliquots of the dissolved targets were diluted with c. HNO.sub.3 and loaded onto approximately 200 mg of resin. The column was subsequently rinsed with c. HNO.sub.3 and eluted with approximately 1.5 mL 0.1 M HNO.sub.3. The contents of the load, wash, and elution fractions were quantified by HPGe to track the retention of the .sup.69Ge.sup.4+ ions on the resin columns and in the different eluates.

Results

[0056] The masses of cobalt powder and chunks of gallium sealed in the ampules were observed to have formed orange-hot, glowing pellets when removed from the furnace immediately prior to quenching. The average change in mass during the pellet forging in the ampules observed initially was less than 5%. The average change in mass during the pellet pressing observed initially was less than 1%. None of the targets showed any appreciable melting or mass loss during the irradiation with up to 5 A of 13 MeV protons. For .sup.69Ge, the first 1:3::Co:Ge atom ratio target irradiated showed an experimental yield of 0.36 mCi/(A h). The targets dissolved in c. HNO.sub.3 produced a dark reddish-brown solution. Initial separation results showed over 60% retention of the .sup.69Ge on the branched DGA resin.

[0057] The word illustrative is used herein to mean serving as an example, instance, or illustration. Any aspect or design described herein as illustrative is not necessarily to be construed as preferred or advantageous over other aspects or designs. Further, for the purposes of this disclosure and unless otherwise specified, a or an means one or more.

[0058] The foregoing description of illustrative embodiments of the invention has been presented for purposes of illustration and of description. It is not intended to be exhaustive or to limit the invention to the precise form disclosed, and modifications and variations are possible in light of the above teachings or may be acquired from practice of the invention. The embodiments were chosen and described in order to explain the principles of the invention and as practical applications of the invention to enable one skilled in the art to utilize the invention in various embodiments and with various modifications as suited to the particular use contemplated. It is intended that the scope of the invention be defined by the claims appended hereto and their equivalents.