Roy Copping
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Roy Copping has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Miguel Toro-González
Oak Ridge National Laboratory
2 shared publications - Saed Mirzadeh
Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
2 shared publications - Allison Peacock
Radioisotope Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37830, USA
1 shared publication - Andrew Miskowiec
Oak Ridge National Laboratory
1 shared publication - David A. Cullen
Oak Ridge National Laboratory
1 shared publication - Jessika Viviana Rojas
Department of Mechanical and Nuclear Engineering, Virginia Commonwealth University, Richmond, USA
1 shared publication
Latest Publications
- Open Access
- 23 January 2021
- Published by MDPI AG in Journal of Nanotheranostics
- Vol. 2 (1) , 33-50
Tailoring the Radionuclide Encapsulation and Surface Chemistry of La(223Ra)VO4 Nanoparticles for Targeted Alpha Therapy
The development of targeted alpha therapy (TAT) as a viable cancer treatment requires innovative solutions to challenges associated with radionuclide retention to enhance local tumor cytotoxicity and to minimize off-target effects. Nanoparticles (NPs) with high encapsulation and high retention of radionuclides have shown potential in overcoming these issues. This article shows the influence of pH on the structure of lanthanum vanadate (LaVO4) NPs and its impact on the radiochemical yield of 223Ra and subsequent retention of its decay daughters, 211Pb and 211Bi. An acidic pH (4.9) results in a high fraction of La(223Ra)VO4 NPs with tetragonal structure (44.6–66.1%) and a 223Ra radiochemical yield 80% of La(223Ra)VO4 NPs with monoclinic structure and increases the 223Ra radiochemical yield >85%. The leakage of decay daughters from La(223Ra)VO4 NPs (pH 11) was 223Ra)VO4 NPs with carboxylate and phosphate compounds resulted in a threefold decrease in hydrodynamic diameter and a 223Ra radiochemical yield between 74.7% and 99.6%. These results show the importance of tailoring the synthesis parameters and surface chemistry of LaVO4 NPs to obtain high encapsulation and retention of radionuclides.
- 23 January 2021
- Published by MDPI AG in Journal of Nanotheranostics
- Vol. 2 (1) , 33-50
Open AccessTailoring the Radionuclide Encapsulation and Surface Chemistry of La(223Ra)VO4 Nanoparticles for Targeted Alpha Therapy
The development of targeted alpha therapy (TAT) as a viable cancer treatment requires innovative solutions to challenges associated with radionuclide retention to enhance local tumor cytotoxicity and to minimize off-target effects. Nanoparticles (NPs) with high encapsulation and high retention of radionuclides have shown potential in overcoming these issues. This article shows the influence of pH on the structure of lanthanum vanadate (LaVO4) NPs and its impact on the radiochemical yield of 223Ra and subsequent retention of its decay daughters, 211Pb and 211Bi. An acidic pH (4.9) results in a high fraction of La(223Ra)VO4 NPs with tetragonal structure (44.6–66.1%) and a 223Ra radiochemical yield 80% of La(223Ra)VO4 NPs with monoclinic structure and increases the 223Ra radiochemical yield >85%. The leakage of decay daughters from La(223Ra)VO4 NPs (pH 11) was 223Ra)VO4 NPs with carboxylate and phosphate compounds resulted in a threefold decrease in hydrodynamic diameter and a 223Ra radiochemical yield between 74.7% and 99.6%. These results show the importance of tailoring the synthesis parameters and surface chemistry of LaVO4 NPs to obtain high encapsulation and retention of radionuclides.
- 13 November 2018
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry B
- Vol. 6 (47) , 7985-7997
Multifunctional GdVO4:Eu core–shell nanoparticles containing225Ac for targeted alpha therapy and molecular imaging
Development of actinium-225 doped Gd0.8Eu0.2VO4core–shell nanoparticles as multifunctional platforms for multimodal molecular imaging and targeted radionuclide therapy.
- 13 November 2018
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry B
- Vol. 6 (47) , 7985-7997
Multifunctional GdVO4:Eu core–shell nanoparticles containing225Ac for targeted alpha therapy and molecular imaging
Development of actinium-225 doped Gd0.8Eu0.2VO4core–shell nanoparticles as multifunctional platforms for multimodal molecular imaging and targeted radionuclide therapy.