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Short life fission products extracted from molten salt reactor fuel for radiopharmaceutical applications

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Short life fission products extracted from molten salt reactor fuel for radiopharmaceutical applications. / Degueldre, Claude; Findlay, Joshua; Cheneler, David et al.
In: Applied Radiation and Isotopes, Vol. 205, 111146, 31.03.2024.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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Degueldre C, Findlay J, Cheneler D, Sardar S, Green S. Short life fission products extracted from molten salt reactor fuel for radiopharmaceutical applications. Applied Radiation and Isotopes. 2024 Mar 31;205:111146. Epub 2023 Dec 27. doi: 10.1016/j.apradiso.2023.111146

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@article{39f8704338d44ee08cc39d7cc6ccd0d3,
title = "Short life fission products extracted from molten salt reactor fuel for radiopharmaceutical applications",
abstract = "This work studies the potential of using short life fission product ( AFp) radioisotopes e.g. 82Br, 86Rb, ( 90Sr) - 90mY, ( 99Mo) - 99mTc, 103Ru - 103mRh, 111Ag, 127Sb - 127(m)Te, 126I, 131I, 133Xe, 136Cs, 141Ce, 143Ce, 143Pr, 147Nd - 147Pm, 149Pm, 153Sm, 156Eu, 159Gd and 161Tb, extracted from a molten salt reactor and their separation using specific thermodynamic and radiochemical conditions. Their utilisation for coupled radiodiagnostics and radiotherapy is a key consideration. A molten salt reactor produces fission products during operation. These radioisotopes can be separated at line from the liquid fuel by evaporation/distillation, chemical reduction (using H 2 doped gas), electro-deposition and/or chemical oxidation (using Cl 2 doped gas). They can be refined and chemically treated for radiopharmaceutical use for imaging and radiodiagnostics utilising γ radioscopy or positron emission tomography, and potentially in radiotherapy to target specific cancers or viral diseases using β − emitters. Some of the AFp isotopes are currently used for radiodiagnostics because they emit γ rays of energy 50–200 keV. However, some may also be used in parallel for radiotherapy utilising their β − (E Mean ≈ 100 keV) emission whose mean free pathway of c.a. 100 nm in biological tissue is much smaller than their penetration depth. Focus is given to 86Rb, 90Y, 99mTc, 131I and 133Xe as well as on the ALn isotopes ( 141Ce, 143Ce - 143Pr, 147Nd - 147Pm, 149Pm and 153Sm) because of their strong potential for complexation with bio-ligands (e.g. DOTA) or for their ability to form micro-nano-spheres, and because of their potential for dual radiodiagnostics and radiotherapy. It is shown that these radio-lanthanides could also replace 177Lu for the treatment of specific cancers.",
author = "Claude Degueldre and Joshua Findlay and David Cheneler and Suneela Sardar and Sarah Green",
year = "2024",
month = mar,
day = "31",
doi = "10.1016/j.apradiso.2023.111146",
language = "English",
volume = "205",
journal = "Applied Radiation and Isotopes",
issn = "0969-8043",
publisher = "Elsevier Limited",

}

RIS

TY - JOUR

T1 - Short life fission products extracted from molten salt reactor fuel for radiopharmaceutical applications

AU - Degueldre, Claude

AU - Findlay, Joshua

AU - Cheneler, David

AU - Sardar, Suneela

AU - Green, Sarah

PY - 2024/3/31

Y1 - 2024/3/31

N2 - This work studies the potential of using short life fission product ( AFp) radioisotopes e.g. 82Br, 86Rb, ( 90Sr) - 90mY, ( 99Mo) - 99mTc, 103Ru - 103mRh, 111Ag, 127Sb - 127(m)Te, 126I, 131I, 133Xe, 136Cs, 141Ce, 143Ce, 143Pr, 147Nd - 147Pm, 149Pm, 153Sm, 156Eu, 159Gd and 161Tb, extracted from a molten salt reactor and their separation using specific thermodynamic and radiochemical conditions. Their utilisation for coupled radiodiagnostics and radiotherapy is a key consideration. A molten salt reactor produces fission products during operation. These radioisotopes can be separated at line from the liquid fuel by evaporation/distillation, chemical reduction (using H 2 doped gas), electro-deposition and/or chemical oxidation (using Cl 2 doped gas). They can be refined and chemically treated for radiopharmaceutical use for imaging and radiodiagnostics utilising γ radioscopy or positron emission tomography, and potentially in radiotherapy to target specific cancers or viral diseases using β − emitters. Some of the AFp isotopes are currently used for radiodiagnostics because they emit γ rays of energy 50–200 keV. However, some may also be used in parallel for radiotherapy utilising their β − (E Mean ≈ 100 keV) emission whose mean free pathway of c.a. 100 nm in biological tissue is much smaller than their penetration depth. Focus is given to 86Rb, 90Y, 99mTc, 131I and 133Xe as well as on the ALn isotopes ( 141Ce, 143Ce - 143Pr, 147Nd - 147Pm, 149Pm and 153Sm) because of their strong potential for complexation with bio-ligands (e.g. DOTA) or for their ability to form micro-nano-spheres, and because of their potential for dual radiodiagnostics and radiotherapy. It is shown that these radio-lanthanides could also replace 177Lu for the treatment of specific cancers.

AB - This work studies the potential of using short life fission product ( AFp) radioisotopes e.g. 82Br, 86Rb, ( 90Sr) - 90mY, ( 99Mo) - 99mTc, 103Ru - 103mRh, 111Ag, 127Sb - 127(m)Te, 126I, 131I, 133Xe, 136Cs, 141Ce, 143Ce, 143Pr, 147Nd - 147Pm, 149Pm, 153Sm, 156Eu, 159Gd and 161Tb, extracted from a molten salt reactor and their separation using specific thermodynamic and radiochemical conditions. Their utilisation for coupled radiodiagnostics and radiotherapy is a key consideration. A molten salt reactor produces fission products during operation. These radioisotopes can be separated at line from the liquid fuel by evaporation/distillation, chemical reduction (using H 2 doped gas), electro-deposition and/or chemical oxidation (using Cl 2 doped gas). They can be refined and chemically treated for radiopharmaceutical use for imaging and radiodiagnostics utilising γ radioscopy or positron emission tomography, and potentially in radiotherapy to target specific cancers or viral diseases using β − emitters. Some of the AFp isotopes are currently used for radiodiagnostics because they emit γ rays of energy 50–200 keV. However, some may also be used in parallel for radiotherapy utilising their β − (E Mean ≈ 100 keV) emission whose mean free pathway of c.a. 100 nm in biological tissue is much smaller than their penetration depth. Focus is given to 86Rb, 90Y, 99mTc, 131I and 133Xe as well as on the ALn isotopes ( 141Ce, 143Ce - 143Pr, 147Nd - 147Pm, 149Pm and 153Sm) because of their strong potential for complexation with bio-ligands (e.g. DOTA) or for their ability to form micro-nano-spheres, and because of their potential for dual radiodiagnostics and radiotherapy. It is shown that these radio-lanthanides could also replace 177Lu for the treatment of specific cancers.

U2 - 10.1016/j.apradiso.2023.111146

DO - 10.1016/j.apradiso.2023.111146

M3 - Journal article

VL - 205

JO - Applied Radiation and Isotopes

JF - Applied Radiation and Isotopes

SN - 0969-8043

M1 - 111146

ER -