Relevant bibliographies by topics / Copper radionuclides

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  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Copper radionuclides'

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Published: 4 June 2021
Last updated: 5 February 2022

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Journal articles on the topic "Copper radionuclides"

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Stephan, Holger, Ralf Bergmann, Jörg Steinbach, Leone Spiccia, and Peter Comba. "Versatile new bifunctional chelators for copper radionuclides." Nuclear Medicine and Biology 37, no. 6 (August 2010): 695. http://dx.doi.org/10.1016/j.nucmedbio.2010.04.086.

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2

Blower, Philip J., Jason S. Lewis, and Jamal Zweit. "Copper radionuclides and radiopharmaceuticals in nuclear medicine." Nuclear Medicine and Biology 23, no. 8 (November 1996): 957–80. http://dx.doi.org/10.1016/s0969-8051(96)00130-8.

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3

Cai, Zhengxin, and Carolyn J. Anderson. "Chelators for copper radionuclides in positron emission tomography radiopharmaceuticals." Journal of Labelled Compounds and Radiopharmaceuticals 57, no. 4 (December 18, 2013): 224–30. http://dx.doi.org/10.1002/jlcr.3165.

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Follacchio, Giulia Anna, Maria Silvia De Feo, Giuseppe De Vincentis, Francesco Monteleone, and Mauro Liberatore. "Radiopharmaceuticals Labelled with Copper Radionuclides: Clinical Results in Human Beings." Current Radiopharmaceuticals 11, no. 1 (April 4, 2018): 22–33. http://dx.doi.org/10.2174/1874471011666171211161851.

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Nakamura, Takashi, Tohru Ohkubo, and Yoshimoto Uwamino. "Spatial distribution of radionuclides produced in copper by photonuclear spallation reactions." Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment 256, no. 3 (May 1987): 505–12. http://dx.doi.org/10.1016/0168-9002(87)90294-4.

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6

McInnes, Lachlan E., Asif Noor, Peter D. Roselt, Catriona A. McLean, Jonathan M. White, and Paul S. Donnelly. "A Copper Complex of a Thiosemicarbazone-Pyridylhydrazone Ligand Containing a Vinylpyridine Functional Group as a Potential Imaging Agent for Amyloid-β Plaques." Australian Journal of Chemistry 72, no. 10 (2019): 827. http://dx.doi.org/10.1071/ch19311.

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Complexes containing positron-emitting radionuclides of copper have the potential to be of use for diagnostic imaging with positron emission tomography. Alzheimer’s disease is characterised by the presence of amyloid-β plaques in the brain. A new thiosemicarbazone-pyridyl hydrazone tetradentate ligand with a pyridyl-4-vinylpyridine functional group was prepared with the aim of making a copper complex that binds to amyloid-β plaques to assist in the diagnosis of Alzheimer’s disease. The ligand forms a charge neutral complex with copper(ii) that was characterised by X-ray crystallography and the electrochemical behaviour of the complex was investigated by cyclic voltammetry. The new ligand can be radiolabelled with positron-emitting copper-64 at room temperature in excellent radiochemical yields. The new complex interacts with synthetic amyloid-β fibrils and binds amyloid-β plaques present in post-mortem Alzheimer’s disease brain tissue.
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7

Idemitsu, Kazuya, Keisuke Yoshida, Yaohiro Inagaki, and Tatsumi Arima. "Migration Behavior of Copper in Compacted Bentonite Using Electromigration Techniques." MRS Advances 5, no. 3-4 (2020): 141–47. http://dx.doi.org/10.1557/adv.2020.55.

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ABSTRACTCopper is a candidate for use as an overpack material in deep underground nuclear waste disposal. Copper, however, is susceptible to corrosion following closure of the repository and migration of the corrosion products through the buffer material may affect the migration of redox-sensitive radionuclides. Electromigration experiments were performed whereby a copper coupon, which was in contact with compacted bentonite, served as the working electrode and was held at a constant potential of between +100 to +400 mV vs. Ag/AgCl electrode for up to 48 h. The amounts of copper that migrated into the bentonite specimens were found to be in good agreement with the calculated values based on the corrosion current flow for the assumption that copper underwent anodic dissolution as Cu(II). A model based on dispersion and electromigration was able to explain the measured copper profiles in the bentonite specimens. The fitted values of the dispersion coefficient did not depend on the applied potential and were about 10-12 m2/s.
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ANTONIOU, Z. K., M. DASSENAKIS, D. PANAGOPOULOS, and E. SOFOULI. "Copper and manganese in loggerhead turtles (Caretta caretta) tissues in the Mediterranean." Mediterranean Marine Science 5, no. 1 (June 1, 2004): 109. http://dx.doi.org/10.12681/mms.215.

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The natural radionuclides 238U ,234Th, 40K and the main man-made 137Cs, have been studied inMytilus galloprovincialis (Lamarck, 1819) sampled in the Thermaikos gulf – North Aegean Sea, considered as a bioindicator for radiological assessment in the Mediterranean. The ratio 234U/238U has also been determined. In terms of 137Cs, the activity concentrations in seawater from the studied area have been measured as well, and the concentration factors of 137Cs in Mytilus galloprovincialis are given as a parameter of the organism response to radioactive pollution.
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Pupillo, Gaia, Liliana Mou, Petra Martini, Micòl Pasquali, Alessandra Boschi, Gianfranco Cicoria, Adriano Duatti, Férid Haddad, and Juan Esposito. "Production of 67Cu by enriched 70Zn targets: first measurements of formation cross sections of 67Cu, 64Cu, 67Ga, 66Ga, 69mZn and 65Zn in interactions of 70Zn with protons above 45 MeV." Radiochimica Acta 108, no. 8 (August 27, 2020): 593–602. http://dx.doi.org/10.1515/ract-2019-3199.

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AbstractDespite its insufficient availability, Copper-67 is currently attracting much attention for its enormous potential for cancer therapy as theranostic radionuclide. This work aims to accurately measure the unexplored cross section 70Zn(p,x)67Cu in the energy range 45–70 MeV and to evaluate its potential advantages in the case of high-intensity proton beams provided by compact cyclotrons. Thin target foils of enriched 70Zn were manufactured by lamination at the INFN-LNL and irradiated at the ARRONAX facility using the stacked-foils method. A radiochemical procedure for the separation of Cu, Ga and Zn contaminants and the isolation of 67Cu from the irradiated material was developed. The efficiency of the chemical processing was determined for each foil by monitoring the activity of selected tracer radionuclides (61Cu, 66Ga and 69mZn) through γ-spectrometry. Experimental data of the 70Zn(p,x)67Cu, 64Cu, 67Ga, 66Ga, 69mZn, 65Zn cross sections were measured for the first time in the energy range 45–70 MeV and compared with the theoretical results obtained by using the TALYS code. The 67Cu production yield by using enriched 70Zn thick targets was compared with the results obtained by using 68Zn targets in the same irradiation conditions.
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Rollog, Mark, Nigel J. Cook, Paul Guagliardo, Kathy Ehrig, Cristiana L. Ciobanu, and Matt Kilburn. "Detection of Trace Elements/Isotopes in Olympic Dam Copper Concentrates by nanoSIMS." Minerals 9, no. 6 (May 30, 2019): 336. http://dx.doi.org/10.3390/min9060336.

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Many analytical techniques for trace element analysis are available to the geochemist and geometallurgist to understand and, ideally, quantify the distribution of trace and minor components in a mineral deposit. Bulk trace element data are useful, but do not provide information regarding specific host minerals—or lack thereof, in cases of surface adherence or fracture fill—for each element. The CAMECA nanoscale secondary ion mass spectrometer (nanoSIMS) 50 and 50L instruments feature ultra-low minimum detection limits (to parts-per-billion) and sub-micron spatial resolution, a combination not found in any other analytical platform. Using ore and copper concentrate samples from the Olympic Dam mining-processing operation, South Australia, we demonstrate the application of nanoSIMS to understand the mineralogical distribution of potential by-product and detrimental elements. Results show previously undetected mineral host assemblages and elemental associations, providing geochemists with insight into mineral formation and elemental remobilization—and metallurgists with critical information necessary for optimizing ore processing techniques. Gold and Te may be seen associated with brannerite, and Ag prefers chalcocite over bornite. Rare earth elements may be found in trace quantities in fluorapatite and fluorite, which may report to final concentrates as entrained liberated or gangue-sulfide composite particles. Selenium, As, and Te reside in sulfides, commonly in association with Pb, Bi, Ag, and Au. Radionuclide daughters of the 238U decay chain may be located using nanoSIMS, providing critical information on these trace components that is unavailable using other microanalytical techniques. These radionuclides are observed in many minerals but seem particularly enriched in uranium minerals, some phosphates and sulfates, and within high surface area minerals. The nanoSIMS has proven a valuable tool in determining the spatial distribution of trace elements and isotopes in fine-grained copper ore, providing researchers with crucial evidence needed to answer questions of ore formation, ore alteration, and ore processing.
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Dissertations / Theses on the topic "Copper radionuclides"

1

Peters, Adam J. "A study of the binding of trace metals and radionuclides by humic substances." Thesis, Lancaster University, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310586.

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Juran, Stefanie. "Entwicklung neuer radioaktiver Kupferkomplexe hoher Stabilität auf der Basis sechszähniger 3,7-Diazabicyclo[3.3.1]nonan-Derivate." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2009. http://nbn-resolving.de/urn:nbn:de:bsz:14-ds-1231326126632-95160.

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Die Entwicklung von Komplexbildnern für Kupferradionuklide im Hinblick auf eine nuklearmedizinische Anwendung ist ein intensiv bearbeitetes und in rascher Entwicklung begriffenes Forschungsgebiet. Dabei spielen verschiedene Faktoren – wie die günstigen kernphysikalischen Eigenschaften der verfügbaren Kupferradionuklide (Halbwertszeit, Umwandlungsart und -energien), die synthetische Zugänglichkeit und Modifizierbarkeit der Liganden sowie Markierungsausbeute und In-vivo-Stabilität der radioaktiven Kupferkomplexe – eine entscheidende Rolle. Liganden auf der Basis des 3,7-Diazabicyclo[3.3.1]nonans (Bispidine) besitzen für derartige radiopharmazeutische Anwendungen ein hohes Potential. Sie bilden mit Cu2+ sehr stabile Koordinationsverbindungen, wobei die Komplexstabilität im Bereich makrocyclischer Chelatoren liegt (logK ~ 20). Ferner weisen Bispidin-Derivate eine schnelle Komplexbildungskinetik mit Cu2+ auf. Damit sind radioaktiv markierte Bispidin-Liganden prinzipiell für einen Einsatz in der Nuklearmedizin (64Cu: Diagnostik, 67Cu: Therapie) geeignet und zwar insbesondere dann, wenn das Ligand-Grundgerüst mit zielsuchenden Biomolekülen, wie spezifischen Peptiden, Antikörpern oder Nukleinsäurebausteinen, funktionalisiert werden kann. Im Rahmen der vorliegenden Arbeit wurden neuartige sechszähnige Bispidin-Derivate mit Pyridyl-, Imidazolyl- und/oder Benzimidazolyl-Donoreinheiten mit Hilfe einer doppelten Mannich-Kondensation synthetisiert sowie koordinationschemisch und spektroskopisch charakterisiert. • Die Darstellung dieser Liganden erfolgte durch eine systematische Variation der Donoreinheiten an den C2/C4-Kohlenstoffatomen sowie den tertiären Aminostickstoffatomen N3/N7. Hierbei wurde insbesondere untersucht, wie sich der Einbau der unterschiedlichen Donorgruppen an den verschiedenen Positionen des Grundgerüsts auf das Löslichkeits- und Komplexbildungsverhalten auswirkt. Auf der Basis NMR-spektroskopischer Untersuchungen konnte gezeigt werden, dass die Einführung von Imidazolyl-Substituenten in N3- und N7 Position ausschließlich zu Isomeren führt, die eine trans-Stellung der Donoreinheiten an den C2/C4-Positionen aufweisen. Demgegenüber ist es möglich, durch den Einbau von Methylimidazolyl-Einheiten an C2 und C4, das im Hinblick auf die Komplexbildung mit Cu2+ gewünschte cis-Isomer zu isolieren. Diese Ergebnisse konnten anhand von Röntgenkristallstrukturanalysen der entsprechenden CuII-Komplexverbindungen bestätigt werden. • Mit Hilfe der Cyclovoltammetrie wurden CuII/CuI-Redoxpotentiale für ausgewählte CuII Bispidinkomplexe bestimmt. Da eine starke Korrelation dieser Redoxpotentiale mit den jeweiligen Stabilitätskonstanten besteht, können auf diese Weise Vorhersagen zur Komplexstabilität getroffen werden. Dabei konnte gezeigt werden, dass Bispidin-Liganden mit Pyridyl-Gruppen an N3/N7 sowie Methylimidazolyl- bzw. Pyridyl-Einheiten an C2/C4 sehr stabile Komplexe mit Cu2+ bilden. Hinsichtlich der synthetischen Zugänglichkeit ergeben sich jedoch für den Pyridyl-substituierten Liganden A Vorteile. Deshalb wurden Untersuchungen zur Biofunktionalisierung an diesem Derivat erprobt. Durch eine selektive Reduktion der Carbonylgruppe in 9-Stellung wurde der entsprechende Monoalkohol (B) als anti-Epimer dargestellt. Dieser Reaktionsschritt implizierte sowohl eine erhöhte chemische Stabilität des Liganden als auch eine gesteigerte Komplexstabilität des korrespondierenden CuII Komplexes. Die Hydrolyse der Methylestergruppen in Anwesenheit von Cäsiumhydroxid führte in hoher Ausbeute zur Verbindung C, welche an C1 und C5 über kupplungsfähige Carboxylgruppen verfügt. • Die Röntgenkristallstrukturen der CuII-Komplexe der Derivate B und C zeigen eine verzerrt oktaedrische Geometrie, wobei eine sechsfache Koordination mit dem Zentralatom vorzufinden ist. Dieser Aspekt führt zu einer nahezu vollständigen Abschirmung des Zentralatoms. Stabilitätsuntersuchungen auf der Basis der UV-Vis-Spektroskopie in Gegenwart des Konkurrenzliganden Glutathion ergaben, dass diese CuII-Komplexe selbst bei einem 100fachen Überschuss an Glutathion über mindestens 24 Stunden stabil sind. • Es wurde eine Reihe von Untersuchungen zur Kupplung von Linkereinheiten und Biomolekülen am Beispiel des Bispidin-Derivates C vollzogen. Im Rahmen der Arbeiten gelang es, Spacereinheiten wie γ-Aminobuttersäure, Ethylendiamin oder auch Maleinimid-Derivate an das Bispidin-Grundgerüst zu kuppeln. Die Funktionalisierung des Rückgrats mit Target-spezifischen Strukturen erfolgte anhand der Peptidsequenzen Neurotensin(8-13) und Bombesin(7-14). Dabei konnte demonstriert werden, dass eine Erhöhung der Ausbeuten an Peptidkonjugat ausgehend von Spacer-funktionalisierten Liganden erzielt werden kann. • Die radioaktive Markierung der Bispidin-Liganden mit den Radionukliden 64/67Cu verläuft unter physiologischen Bedingungen innerhalb weniger Minuten in hohen radiochemischen Ausbeuten (≥ 99%). In-vitro-Stabilitätsuntersuchungen (Rattenplasma, Challenge-Experimente mit Superoxid-Dismutase) an 64Cu-markierten Bispidin-Liganden und entsprechenden Peptidkonjugaten belegen, dass das Radionuklid über einen Zeitraum von 24 Stunden stabil gebunden bleibt. • Im Rahmen von In-vivo-Studien erfolgten Bioverteilungsuntersuchungen sowie Kleintier-PET-Aufnahmen an verschiedenen Bispidin-Derivaten. Das Bioverteilungsmuster der radiomarkierten Ligand- und Peptidkonjugat-Komplexe in männlichen Wistar-Ratten zeigte eine schnelle renale Ausscheidung der Verbindungen. Metabolitenanalysen bestätigten eine hohe In-vivo-Stabilität der 64Cu Bispidin-Komplexe. PET-Studien an PC3-Tumor-Mäusen unter Einsatz des 64Cu markierten Bispidin-Bombesin-Derivates belegen eine gute Tumoranreicherung dieser Verbindung sowie eine klare Visualisierung des Tumors.
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3

Juran, Stefanie. "Entwicklung neuer radioaktiver Kupferkomplexe hoher Stabilität auf der Basis sechszähniger 3,7-Diazabicyclo[3.3.1]nonan-Derivate." Doctoral thesis, Technische Universität Dresden, 2008. https://tud.qucosa.de/id/qucosa%3A23626.

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Die Entwicklung von Komplexbildnern für Kupferradionuklide im Hinblick auf eine nuklearmedizinische Anwendung ist ein intensiv bearbeitetes und in rascher Entwicklung begriffenes Forschungsgebiet. Dabei spielen verschiedene Faktoren – wie die günstigen kernphysikalischen Eigenschaften der verfügbaren Kupferradionuklide (Halbwertszeit, Umwandlungsart und -energien), die synthetische Zugänglichkeit und Modifizierbarkeit der Liganden sowie Markierungsausbeute und In-vivo-Stabilität der radioaktiven Kupferkomplexe – eine entscheidende Rolle. Liganden auf der Basis des 3,7-Diazabicyclo[3.3.1]nonans (Bispidine) besitzen für derartige radiopharmazeutische Anwendungen ein hohes Potential. Sie bilden mit Cu2+ sehr stabile Koordinationsverbindungen, wobei die Komplexstabilität im Bereich makrocyclischer Chelatoren liegt (logK ~ 20). Ferner weisen Bispidin-Derivate eine schnelle Komplexbildungskinetik mit Cu2+ auf. Damit sind radioaktiv markierte Bispidin-Liganden prinzipiell für einen Einsatz in der Nuklearmedizin (64Cu: Diagnostik, 67Cu: Therapie) geeignet und zwar insbesondere dann, wenn das Ligand-Grundgerüst mit zielsuchenden Biomolekülen, wie spezifischen Peptiden, Antikörpern oder Nukleinsäurebausteinen, funktionalisiert werden kann. Im Rahmen der vorliegenden Arbeit wurden neuartige sechszähnige Bispidin-Derivate mit Pyridyl-, Imidazolyl- und/oder Benzimidazolyl-Donoreinheiten mit Hilfe einer doppelten Mannich-Kondensation synthetisiert sowie koordinationschemisch und spektroskopisch charakterisiert. • Die Darstellung dieser Liganden erfolgte durch eine systematische Variation der Donoreinheiten an den C2/C4-Kohlenstoffatomen sowie den tertiären Aminostickstoffatomen N3/N7. Hierbei wurde insbesondere untersucht, wie sich der Einbau der unterschiedlichen Donorgruppen an den verschiedenen Positionen des Grundgerüsts auf das Löslichkeits- und Komplexbildungsverhalten auswirkt. Auf der Basis NMR-spektroskopischer Untersuchungen konnte gezeigt werden, dass die Einführung von Imidazolyl-Substituenten in N3- und N7 Position ausschließlich zu Isomeren führt, die eine trans-Stellung der Donoreinheiten an den C2/C4-Positionen aufweisen. Demgegenüber ist es möglich, durch den Einbau von Methylimidazolyl-Einheiten an C2 und C4, das im Hinblick auf die Komplexbildung mit Cu2+ gewünschte cis-Isomer zu isolieren. Diese Ergebnisse konnten anhand von Röntgenkristallstrukturanalysen der entsprechenden CuII-Komplexverbindungen bestätigt werden. • Mit Hilfe der Cyclovoltammetrie wurden CuII/CuI-Redoxpotentiale für ausgewählte CuII Bispidinkomplexe bestimmt. Da eine starke Korrelation dieser Redoxpotentiale mit den jeweiligen Stabilitätskonstanten besteht, können auf diese Weise Vorhersagen zur Komplexstabilität getroffen werden. Dabei konnte gezeigt werden, dass Bispidin-Liganden mit Pyridyl-Gruppen an N3/N7 sowie Methylimidazolyl- bzw. Pyridyl-Einheiten an C2/C4 sehr stabile Komplexe mit Cu2+ bilden. Hinsichtlich der synthetischen Zugänglichkeit ergeben sich jedoch für den Pyridyl-substituierten Liganden A Vorteile. Deshalb wurden Untersuchungen zur Biofunktionalisierung an diesem Derivat erprobt. Durch eine selektive Reduktion der Carbonylgruppe in 9-Stellung wurde der entsprechende Monoalkohol (B) als anti-Epimer dargestellt. Dieser Reaktionsschritt implizierte sowohl eine erhöhte chemische Stabilität des Liganden als auch eine gesteigerte Komplexstabilität des korrespondierenden CuII Komplexes. Die Hydrolyse der Methylestergruppen in Anwesenheit von Cäsiumhydroxid führte in hoher Ausbeute zur Verbindung C, welche an C1 und C5 über kupplungsfähige Carboxylgruppen verfügt. • Die Röntgenkristallstrukturen der CuII-Komplexe der Derivate B und C zeigen eine verzerrt oktaedrische Geometrie, wobei eine sechsfache Koordination mit dem Zentralatom vorzufinden ist. Dieser Aspekt führt zu einer nahezu vollständigen Abschirmung des Zentralatoms. Stabilitätsuntersuchungen auf der Basis der UV-Vis-Spektroskopie in Gegenwart des Konkurrenzliganden Glutathion ergaben, dass diese CuII-Komplexe selbst bei einem 100fachen Überschuss an Glutathion über mindestens 24 Stunden stabil sind. • Es wurde eine Reihe von Untersuchungen zur Kupplung von Linkereinheiten und Biomolekülen am Beispiel des Bispidin-Derivates C vollzogen. Im Rahmen der Arbeiten gelang es, Spacereinheiten wie γ-Aminobuttersäure, Ethylendiamin oder auch Maleinimid-Derivate an das Bispidin-Grundgerüst zu kuppeln. Die Funktionalisierung des Rückgrats mit Target-spezifischen Strukturen erfolgte anhand der Peptidsequenzen Neurotensin(8-13) und Bombesin(7-14). Dabei konnte demonstriert werden, dass eine Erhöhung der Ausbeuten an Peptidkonjugat ausgehend von Spacer-funktionalisierten Liganden erzielt werden kann. • Die radioaktive Markierung der Bispidin-Liganden mit den Radionukliden 64/67Cu verläuft unter physiologischen Bedingungen innerhalb weniger Minuten in hohen radiochemischen Ausbeuten (≥ 99%). In-vitro-Stabilitätsuntersuchungen (Rattenplasma, Challenge-Experimente mit Superoxid-Dismutase) an 64Cu-markierten Bispidin-Liganden und entsprechenden Peptidkonjugaten belegen, dass das Radionuklid über einen Zeitraum von 24 Stunden stabil gebunden bleibt. • Im Rahmen von In-vivo-Studien erfolgten Bioverteilungsuntersuchungen sowie Kleintier-PET-Aufnahmen an verschiedenen Bispidin-Derivaten. Das Bioverteilungsmuster der radiomarkierten Ligand- und Peptidkonjugat-Komplexe in männlichen Wistar-Ratten zeigte eine schnelle renale Ausscheidung der Verbindungen. Metabolitenanalysen bestätigten eine hohe In-vivo-Stabilität der 64Cu Bispidin-Komplexe. PET-Studien an PC3-Tumor-Mäusen unter Einsatz des 64Cu markierten Bispidin-Bombesin-Derivates belegen eine gute Tumoranreicherung dieser Verbindung sowie eine klare Visualisierung des Tumors.
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4

Guddehalli, Parameswarappa Sharavathi. "Bifunctional cyclooctynes in copper-free click chemistry for applications in radionuclide chemistry nd 4-Alkylpyridine derivatives in intramolecular dearomatization and heterocycle synthesis." Diss., University of Iowa, 2011. https://ir.uiowa.edu/etd/2710.

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Part A. Bifunctional cyclooctynes in copper-free click chemistry for applications in radionuclide chemistry: A new monofluorinated cyclooctyne (MFCO) with a reasonable kinetic profile was synthesized in three steps. We have demonstrated that MFCO can be used as a lynchpin to conjugate biomolecules to radionuclide chelators using copper-free 1,3-dipolar cycloaddition reactions with azides. Many bifunctional biomolecule-chelators were synthesized, and then radiolabelled with very high radiochemical purity and specific activity. MFCO-amine analogues were also synthesized and used in construction of chelator-biomolecule conjugates (particularly, NDP-α-MSH analogues) for applications in radioimaging. Bis-MFCO based bivalent ligands with various linker lengths were also synthesized as precursors to multivalent ligands for use in cancer diagnosis and therapy. Part B. 4-Alkylpyridine derivatives in intramolecular dearomatization and heterocycle synthesis: 4-Alkylpyridine derivatives substituted with different carbon nucleophiles were synthesized and subjected to intramolecular spirocyclization under various conditions to afford synthetically useful diazaspiro[4.5]decanes as well as diazaspiro[5.5]undecanes in good yields. The same 4-alkyl substrates were used to synthesize anhydrobase intermediates which, then participated in aldol-like condensation in the presence of Lewis acid to yield highly conjugated dihydropyridines. Acid hydrolysis produced substituted pyridines tethered with functionalized butyro- and valero lactams. The synthesis of related azaspiro[4.5]decanes and azaspiro[5.5]undecanes from reaction of hypervalent iodine reagents with 4-methoxy-substituted benzyl and phenethyl substrates linked to β-keto amide nucleophiles was also briefly investigated.
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5

Liu, Longcheng. "Oxidative Dissolution of Spent Fuel and Release of Nuclides from a Copper/Iron Canister : Model Developments and Applications." Doctoral thesis, KTH, Kemiteknik, 2001. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-3292.

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Three models have been developed and applied in the performance assessment of a final repository. They are based on accepted theories and experimental results for known and possible mechanisms that may dominate in the oxidative dissolution of spent fuel and the release of nuclides from a canister. Assuming that the canister is breached at an early stage after disposal, the three models describe three sub-systems in the near field of the repository, in which the governing processes and mechanisms are quite different. In the model for the oxidative dissolution of the fuel matrix, a set of kinetic descriptions is provided that describes the oxidative dissolution of the fuel matrix and the release of the embedded nuclides. In particular, the effect of autocatalytic reduction of hexavalent uranium by dissolved H2, using UO2 (s) on the fuel pellets as a catalyst, is taken into account. The simulation results suggest that most of the radiolytic oxidants will be consumed by the oxidation of the fuel matrix, and that much less will be depleted by dissolved ferrous iron. Most of the radiolytically produced hexavalent uranium will be reduced by the autocatalytic reaction with H2 on the fuel surface. It will reprecipitate as UO2 (s) on the fuel surface, and thus very little net oxidation of the fuel will take place. In the reactive transport model, the interactions of multiple processes within a defective canister are described, in which numerous redox reactions take place as multiple species diffuse. The effect of corrosion of the cast iron insert of the canister and the reduction of dissolved hexavalent uranium by ferrous iron sorbed onto iron corrosion products and by dissolved H2 are particularly included. Scoping calculations suggest that corrosion of the iron insert will occur primarily under anaerobic conditions. The escaping oxidants from the fuel rods will migrate toward the iron insert. Much of these oxidants will, however, be consumed by ferrous iron that comes from the corrosion of iron. The nonscavenged hexavalent uranium will be reduced by ferrous iron sorbed onto the iron corrosion products and by dissolved hydrogen. In the transport resistance network model, the transport of reactive actinides in the near field is simulated. The model describes the transport resistance in terms of coupled resistors by a coarse compartmentalisation of the repository, based on the concept that various ligands first come into the canister and then diffuse out to the surroundings in the form of nuclide complexes. The simulation results suggest that carbonate accelerates the oxidative dissolution of the fuel matrix by stabilizing uranyl ions, and that phosphate and silicate tend to limit the dissolution by the formation of insoluble secondary phases. The three models provide powerful tools to evaluate "what if" situations and alternative scenarios involving various interpretations of the repository system. They can be used to predict the rate of release of actinides from the fuel, to test alternative hypotheses and to study the response of the system to various parameters and conditions imposed upon it.
QC 20100521
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Mattová, Jana. "Chelatující polymery pro léčbu Wilsonovy nemoci." Doctoral thesis, 2017. http://www.nusl.cz/ntk/nusl-266287.

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Wilson's disease is a hereditary disorder of copper metabolism, which causes copper accumulation in organism, especially in the liver, kidneys and brain. Current treatment is based on using low-molecular weight copper chelators and high doses of zinc salts. Unfortunately, they can induce some severe side effects due to systemic action. The aim of this thesis is to improve the treatment of Wilson's disease by using of polymeric drug delivery systems. The size of polymer particles in tens of microns should provide non-resorbability of the drug after oral administration. Synthetic microparticles of poly(glycidyl methacrylate-co- ethylene dimethacrylate), natural microcrystalline cellulose and cross-linked chitosan were used as polymer matrices. N,N-di(2-pyridylmethyl)amine, triethylenetetraamine and 8-hydroxyquinoline were selected as specific copper chelators, which can complex copper cations with high efficiency. The principle of the proposed treatment is that the polymeric carrier-bound chelator complex copper directly from the food in digestive tract of the organism. Because of non-resorbability, the entire complex should be eliminated from the body together with stools. This virtually eliminates systemic side effects. The ability of adsorption of copper and the stability of polymer complex under...
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Lan, Der-Jang, and 藍得彰. "Ⅰ.Characterization and Removal of Radionuclide 60Co from the Sediment Using Microwave Energy Ⅱ.A Study for Determination of Copper, Lead, Cadmium, Nickel and Chromium in Fly Ash and Bottom Ash from Municipal Waste Incinerator by Microwave Digestion with." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/89166396648334244933.

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碩士
淡江大學
水資源及環境工程學系
87
Ⅰ. Characterization and Removal of Radionuclide 60Co from the Sediment Using Microwave Energy The goals of this study are to characterize the radionuclides 60Co absorbed on soil and to remove this metal from contaminated soil by microwave treatment. This study is concentrated on the application of microwave oven for chemical extraction of radionuclide 60Co in soil. The various experimental condition (microwave power, organic reagents, chelating agent, extraction time, and extraction sequences) were explored and optimized to improve the removing efficiency. The results showed that the removal of 60Co was 42.76% after microwave treatment with ammonium oxalate solution. However, the microwave removing efficiency of 60Co with ammonium oxalate solution twice were improved and increased to 72.37%. The microwave treatment has advantages of simple operation, decrease processing time and low cost equipment required. Ⅱ.A Study for Determination of Copper, Lead, Cadmium, Nickel and Chromium in Fly Ash and Bottom Ash from Municipal Waste Incinerator by Microwave Digestion with Inductively Coupled Plasma-Atomic Emission Spectrometry The traditional techniques for sample preparation such as alkaline fusion and aqua regia dissolution will take many hours to digest the ash samples. In contrast, the samples digested by microwave energy are fast due to the increased heating that occurs from the microwave interaction with the reagents and samples. Therefore, microwave digestion procedures are becoming more popular as they considerably reduce the amount of time spent preparing the sample for the spectrometric analysis. This study was based on modified USEPA Method 3052 and the operating conditions as microwave power, the type and the concentration of acids, the numbers of digestion and digestion time were explored and optimized to digest the ashes from municipal waste incineration completely. The conditions of microwave digesting methods were as following: 0.2g sample was weighed into a vessel and added with 3mL HNO3, 1mL each of HCl and HF. The microwave digestion system was programmed as that of Method 3052. After completion of the microwave program and cooling to room temperature, 10mL of H3BO3 was added to the vessel. The system was programmed again as the same parameters. The results were in good agreement with certified reference material (BCR No. 176), and successfully applied to the determination of copper, lead, cadmium, nickel and chromium in fly ash and bottom ash from municipal waste incineration.
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Book chapters on the topic "Copper radionuclides"

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Anderson, Carolyn J., Mark A. Green, and Yasuhisa Fujibayashi. "Chemistry of Copper Radionuclides and Radiopharmaceutical Products." In Handbook of Radiopharmaceuticals, 401–22. Chichester, UK: John Wiley & Sons, Ltd, 2005. http://dx.doi.org/10.1002/0470846380.ch12.

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Alberto, R., and H. Braband. "SPECT/PET Imaging with Technetium, Gallium, Copper, and Other Metallic Radionuclides." In Comprehensive Inorganic Chemistry II, 785–817. Elsevier, 2013. http://dx.doi.org/10.1016/b978-0-08-097774-4.00331-4.

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"Some of these could also be operated in the energy range above lOMeV for experiments designed to determine at which energy level radioactivity can be induced in the irradiated medium. A linac with a maximum energy of 25 MeV was commissioned for the U.S. Army Natick Research and Development Labora­ tories in 1963. Its beam power was 6.5 kW at an electron energy of 10 MeV, 18 kW at 24 MeV. Assuming 100% efficiency, a 1-kW beam can irradiate 360 kg of product with a dose of 10 kGy/h. The efficiency of electron accelerators is higher than that of gamma sources because the electron beam can be directed at the product, whereas the gamma sources emit radiation in all directions. An efficiency of 50% is a realistic assumption for accelerator facilities. With that and 6.5 kW beam power an accelerator of the type built for the Natick laboratories can process about 1.2t/h at 10 kGy. In Odessa in the former Soviet Union, now in the Ukraine, two 20-kW accelerators with an energy of 1.4 MeV installed next to a grain elevator went into operation in 1983. Each accelerator has the capacity to irradiate 200 t of wheat per hour with a dose of 200 Gy for insect disinfestation. This corresponds to a beam utilization of 56% (9). In France, a facility for electron irradiation of frozen deboned chicken meat commenced operation at Berric near Vannes (Brittany) in late 1986. The purpose of irradiation is to improve the hygienic quality of the meat by destroying salmonella and other disease-causing (pathogenic) microorganisms. The electron beam accelerator is a 7 MeV/10 kW Cassitron built by CGR-MeV (10). An irradiation facility of this type is shown in Figure . Because of their relatively low depth of penetration electron beams cannot be used for the irradiation of animal carcasses, large packages, or other thick materials. However, this difficulty can be overcome by converting the electrons to x-rays. As indicated in Figure 9, this can be done by fitting a water-cooled metal plate to the scanner. Whereas in conventional x-ray tubes the conversion of electron energy to x-ray energy occurs only with an efficiency of about %, much higher efficiencies can be achieved in electron accelerators. The conversion efficiency depends on the material of the converter plate (target) and on the electron energy. Copper converts 5-MeV electrons with about 7% efficiency, 10-MeV electrons with 12% efficiency. A tungsten target can convert 5-MeV electrons with about 20%, 10-MeV electrons with 30% efficiency. (Exact values depend on target thickness.) In contrast to the distinct gamma radiation energy emitted from radionuclides and to the monoenergetic electrons produced by accelerators, the energy spectrum of x-rays is continuous from the value equivalent to the energy of the bombarding electrons to zero. The intensity of this spectrum peaks at about one-tenth of the maximum energy value. The exact location of the intensity peak depends on the thickness of the converter plate and on some other factors. As indicated in Figure." In Safety of Irradiated Foods, 40. CRC Press, 1995. http://dx.doi.org/10.1201/9781482273168-31.

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Conference papers on the topic "Copper radionuclides"

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Avramenko, Valentin, Svetlana Bratskaya, Veniamin Zheleznov, Irina Sheveleva, Dmitry Marinin, and Valentin Sergienko. "Latex Particles Functionalized With Transition Metals Ferrocyanides for Cesium Uptake and Decontamination of Solid Bulk Materials." In ASME 2010 13th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2010. http://dx.doi.org/10.1115/icem2010-40302.

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Decontamination of spent ion-exchange resins, corrosion-unstable metal structures, soil, ground, and construction materials contaminated by fission, corrosion and transuranic radionuclides remains one of the most urgent and complicated ecological problems. Among the existing methods having different efficiencies in regard to such materials decontamination, application of selective sorbents put into a humid medium to be decontaminated (ground, bulk materials) appears to be rather extensive. However, the efficiency of such an approach is significantly limited by difficulties concerned with uniform sorbent distribution in porous media and completeness of spent sorbents removal for final disposal. In this paper we suggest a principally new approach to preparation of colloid-stable selective sorbents for cesium uptake using immobilization of transition metals (cobalt, nickel, and copper) ferrocyanides in nanosized carboxylic latex emulsions. The effects of ferrocyanide composition, pH, and media salinity on the sorption properties of the colloid-stable sorbents toward cesium ions were studied in solutions containing up to 200 g/1 sodium nitrate or potassium chloride. The sorption capacities of the colloid sorbents based on mixed potassium/transition metals ferrocyanides were in the range 1.45–1.86 mol Cs/mol ferrocyanide with the highest value found for the copper ferrocyanide. It was shown that the obtained colloid-stable sorbents were capable to penetrate through bulk materials without filtration that makes them applicable for decontamination of solids, e.g. soils, zeolites, spent ion-exchange resins contaminated with cesium radionuclides. After decontamination of liquid or solid radioactive wastes the colloid-stable sorbents can be easily separated from solutions by precipitation with cationic flocculants providing localization of radionuclides in a small volume of the precipitates formed. Besides, functionalized latex particles can be used for preparation of carbon fiber/ferrocyanide composite materials for cesium uptake using electrodeposition method. Application of the carbon fibers as an inert support for ferrocyanides, in general, significantly improves the sorption kinetics, but washing out of ferrocyanide fines from the fiber surface limits the potential of such materials. When ferrocyanides are deposited in a form of nanocrystals stabilized by latexes which undergo electropolymerization on the fiber surface, the thin polymeric film formed substantially improves the stability of the composite and prevents loss of ferrocyanide during sorbent application. The effect of electrodeposition conditions on composite morphology, ferrocyanide loading and cesium distribution coefficient in media with different salinity has been discussed.
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Parish, Theodore A., and Anthony P. Belian. "Measured radionuclide production from copper, gold and lead spallation targets." In The international conference on accelerator-driven transmutation technologies and applications. AIP, 1995. http://dx.doi.org/10.1063/1.49058.

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