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Omokawa, Marina*; Kimura, Hiroyuki*; Hatsukawa, Yuichi*; Kawashima, Hidekazu*; Tsukada, Kazuaki; Yagi, Yusuke*; Naito, Yuki*; Yasui, Hiroyuki*
Bioorganic & Medicinal Chemistry, 97, p.117557_1 - 117557_6, 2024/01
Times Cited Count:0 Percentile:0.01(Biochemistry & Molecular Biology)Iimura, Shun*; Rosenbusch, M.*; Takamine, Aiko*; Tsunoda, Yusuke*; Wada, Michiharu*; Chen, S.*; Hou, D. S.*; Xian, W.*; Ishiyama, Hironobu*; Yan, S.*; et al.
Physical Review Letters, 130(1), p.012501_1 - 012501_6, 2023/01
Times Cited Count:5 Percentile:94.66(Physics, Multidisciplinary)Hatsukawa, Yuichi*; Hayakawa, Takehito*; Tsukada, Kazuaki; Hashimoto, Kazuyuki*; Sato, Tetsuya; Asai, Masato; Toyoshima, Atsushi; Tanimori, Toru*; Sonoda, Shinya*; Kabuki, Shigeto*; et al.
PLOS ONE (Internet), 13(12), p.e0208909_1 - e0208909_12, 2018/12
Times Cited Count:3 Percentile:30.05(Multidisciplinary Sciences)Imaging of Tc radioisotope was conducted using an electron tracking-Compton camera (ETCC). Tc emits 204, 582, and 835 keV rays, and was produced in the Mo(p,n)Tc reaction with a Mo-enriched target. The recycling of the Mo-enriched molybdenum trioxide was investigated, and the recycled yield of Mo was achieved to be 70% - 90%. The images were obtained with each of the three rays. Results showed that the spatial resolution increases with increasing -ray energy, and suggested that the ETCC with high-energy -ray emitters such as Tc is useful for the medical imaging of deep tissue and organs in the human body.
Ito, Yuta*; Schury, P.*; Wada, Michiharu*; Arai, Fumiya*; Haba, Hiromitsu*; Hirayama, Yoshikazu*; Ishizawa, Satoshi*; Kaji, Daiya*; Kimura, Sota*; Koura, Hiroyuki; et al.
Physical Review Letters, 120(15), p.152501_1 - 152501_6, 2018/04
Times Cited Count:60 Percentile:93.36(Physics, Multidisciplinary)Masses of Es, Fm and the transfermium nuclei Md, and No, produced by hot- and cold-fusion reactions, in the vicinity of the deformed neutron shell closure, have been directly measured using a multi-reflection time-of-flight mass spectrograph. The masses of Es and Md were measured for the first time. Using the masses of Md as anchor points for decay chains, the masses of heavier nuclei, up to Bh and Mt, were determined. These new masses were compared with theoretical global mass models and demonstrated to be in good agreement with macroscopic-microscopic models in this region. The empirical shell gap parameter derived from three isotopic masses was updated with the new masses and corroborate the existence of the deformed neutron shell closure for Md and Lr.
Schury, P.*; Wada, Michiharu*; Ito, Yuta*; Kaji, Daiya*; Haba, Hiromitsu*; Hirayama, Yoshikazu*; Kimura, Sota*; Koura, Hiroyuki; MacCormick, M.*; Miyatake, Hiroari*; et al.
Nuclear Instruments and Methods in Physics Research B, 407, p.160 - 165, 2017/06
Times Cited Count:14 Percentile:78.05(Instruments & Instrumentation)Various isotopes of Ac, Ra, Fr, and Rn were produced by fusion-evaporation reactions using a Ca beam. The energetic ions were stopped in and extracted from a helium gas cell. The extracted ions were identified using a multi-reflection time-of-fight mass spectrograph. In all cases, it was observed that the predominant charge state for the extracted ions, including the alkali Fr, was 2+.
Schury, P.*; Wada, Michiharu*; Ito, Yuta*; Kaji, Daiya*; Arai, Fumiya*; MacCormick, M.*; Murray, I.*; Haba, Hiromitsu*; Jeong, S.*; Kimura, Sota*; et al.
Physical Review C, 95(1), p.011305_1 - 011305_6, 2017/01
Times Cited Count:48 Percentile:96.07(Physics, Nuclear)Using a multireflection time-of-flight mass spectrograph located after a gas cell coupled with the gas-filled recoil ion separator GARIS-II, the masses of several -decaying heavy nuclei were directly and precisely measured. The nuclei were produced via fusion-evaporation reactions and separated from projectilelike and targetlike particles using GARIS-II before being stopped in a helium-filled gas cell. Time-of-flight spectra for three isobar chains, Fr-Rn-At-Po, Fr- Rn-At-Po-Bi, and Fr-Rn-At, were observed. Precision atomic mass values were determined for Fr, Rn, and At. Identifications of Bi, Po, Rn, and At were made with N10 detected ions, representing the next step toward use of mass spectrometry to identify exceedingly low-yield species such as superheavy element ions.
Hatsukawa, Yuichi; Hashimoto, Kazuyuki; Tsukada, Kazuaki; Sato, Tetsuya; Asai, Masato; Toyoshima, Atsushi; Nagai, Yasuki; Tanimori, Toru*; Sonoda, Shinya*; Kabuki, Shigeto*; et al.
Journal of Radioanalytical and Nuclear Chemistry, 303(2), p.1283 - 1285, 2015/02
Times Cited Count:2 Percentile:17.57(Chemistry, Analytical)Technetium-99m (Tc) is used in radioactive medical diagonostic tests, for example as a radioactive tracer that medical equipment can detect in the human body. It is well suited to the role because it emits readily detectable 141 keV rays, and its half-life is 6.01 hours (meaning that about 94% of it decays to technetium-99 in 24 hours). There are at least 31 commonly used radiopharmaceuticals based on technetium-99m for imaging and functional studies of the brain, myocardium, thyroid, lungs, liver, gallbladder, kidneys, skeleton, blood, and tumors. Recent years, with the develop-ment of the Compton camera which can realize high position resolution, technetium isotopes emitting high energy -rays are required. In this study, technetium-95m which emits some rays around 800 keV was produced by the Mo(p,n)Tc reaction.
Ogawa, Kazuma*; Kawashima, Hidekazu*; Kinuya, Seigo*; Shiba, Kazuhiro*; Onoguchi, Masahisa*; Kimura, Hiroyuki*; Hashimoto, Kazuyuki; Odani, Akira*; Saji, Hideo*
Annals of Nuclear Medicine, 23(10), p.843 - 848, 2009/12
Times Cited Count:9 Percentile:31.42(Radiology, Nuclear Medicine & Medical Imaging)Rhenium is one of the most valuable elements for internal radiotherapy because Re have favorable physical characteristics. However, there are problems when proteins such as antibodies are used as carriers of Re. Labeling methods require the complicated processes. Therefore, we planned the preparation by a simple method and evaluation of a stable Re-labeled antibody. For this purpose, we selected Re(I) tricarbonyl complex as a chelating site. A7 was used as a model protein. Re-labeled A7 was prepared by directly reacting a Re(I) tricarbonyl precursor with A7. Re-(CO)-A7 were prepared with radiochemical yields of 23-28%. After purification, Re-(CO)-A7 showed a radiochemical purity of over 95%. In biodistribution experiments, Re-labeled A7 showed high uptakes in the tumor.
Ogawa, Kazuma*; Kawashima, Hidekazu*; Kinuya, Seigo*; Yoshimoto, Mitsuyoshi*; Shiba, Kazuhiro*; Kimura, Hiroyuki*; Hashimoto, Kazuyuki; Mori, Hirofumi*; Saji, Hideo*
no journal, ,
Re is one of the most useful radionuclides for internal radiotherapy. However, there is a problem when protein such as antibody is used as a carrier of Re. The labeling method using bifunctional chelating agents require the conjugation of Re-complex to protein after radiolabeling with the bifunctional chelating agent. Then, we planned the preparation of a stable Re-labeled protein by a simple method. A7 monoclonal antibody was labeled by reacting Re(I) tricarbonyl precursor with A7 directly. Re labeled A7 was prepared with radiochemical yield of 23%. After purification, Re labeled A7 showed radiochemical purity over 98%. After 24 hours of incubation, about 93% of Re-A7 remained intact, which indicates Re-A7 is stable in vitro. In biodistribution experiment, 11.2% of the injected dose/g of Re-A7 accumulated in the tumor at 24 hours postinjection, and tumor to blood ratio was over 1.0 at the same time.
Hirasawa, Makoto*; Kawashima, Hidekazu*; Ogawa, Kazuma*; Kimura, Hiroyuki*; Ono, Masahiro*; Hashimoto, Kazuyuki; Saji, Hideo*
no journal, ,
no abstracts in English
Kawashima, Hidekazu*; Hirasawa, Makoto*; Kimura, Hiroyuki*; Ono, Masahiro*; Hashimoto, Kazuyuki; Saji, Hideo*
no journal, ,
no abstracts in English
Sonoda, Shinya*; Nabetani, Akira*; Kimura, Hiroyuki*; Kabuki, Shigeto*; Takada, Atsushi*; Kubo, Hidetoshi*; Komura, Shotaro*; Sawano, Tatsuya*; Tanimori, Toru*; Matsuoka, Yoshihiro*; et al.
no journal, ,
We present the performance results using this new ETCC such as the imaging test using F-18 in point-like and rod-like phantoms with varying the intense of radiation. In addition, the measurementof Tc-95m which is produced by Japan Atomic Energy Agency was performed. Tc-95m emitsthe -rays with the energy, 204, 583, and 835 keV, and then an image with multi-energies is examined. The position resolution achieves less than about 8 degrees from 10 degrees at 511 keV by this improvement. Further improvement of the angular resolution (position resolution) will be presented until 2015 spring. Also, we are developing the next ETCC by increasing the thickness of the scintillator from 1 rad. to 2 rad. and the gas pressure from 1 atm to 3 atm which improvethe detection efficiency by a factor of 5 at 511 keV. By these improvements, the imaging time of mouse is expected to be reduced from several hours with to 20 minutes for lots of kinds of RIs with the energy band from 0.1-2 MeV.
Hatsukawa, Yuichi; Tsukada, Kazuaki; Hashimoto, Kazuyuki; Sato, Tetsuya; Asai, Masato; Toyoshima, Atsushi; Nagai, Yasuki; Tanimori, Toru*; Sonoda, Shinya*; Kabuki, Shigeto*; et al.
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In recent years, the Compton camera which is originally developed for the astrophysical studies was applied for medical diagnostic usage. For the Compton camera imaging require technetium isotopes emitting higher energy -rays. Two Tc isotopes, Tc (T = 60 d; E = 204, 582 and 835 keV) and Tc(T = 4.28 d, E = 778 and 812 keV) are candidates for Compton camera imaging. Compton camera imaging can realize high position resolution without collimator. Because of no collimator using, the Compton camera makes higher -ray detection efficiency. Compared with SPECT with Tc, the Compton camera imaging technique can be expected that radiation exposure deduce to 1/5-1/10. In this study, technetium-95m was produced by the Mo(p,n)Tc reaction.
Nakamura, Satoshi; Ban, Yasutoshi; Sugimoto, Mie; Tambo, Masaki; Fukaya, Hiroyuki; Hiruta, Kenta; Yoshida, Takuya; Uehara, Hiroyuki; Obata, Hiroki; Kimura, Yasuhiko; et al.
no journal, ,
In Nuclear Science Research Institute at JAEA, detailed studies with regard to the elemental and nuclide compositions of fuel debris have been proceeding. We have conducted dissolution of the samples by alkaline fusion with sodium peroxide and chemical analysis by ICP-AES, alpha and gamma spectrometer, and TIMS. After studying the dissolution methods with various types of simulated debris, a demonstration test with TMI-2 debris was conducted. The elemental composition in the dissolved solution of TMI-2 debris consistent with the results of SEM/WDX and XRD analyses, and the validity of the present method was confirmed. In this presentation, the details of each analysis and the issues raised through the analysis will be introduced.