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61.
Theranostics is a precision medicine which integrates diagnostic nuclear medicine and radionuclide therapy for various cancers throughout body using suitable tracers and treatment that target specific biological pathways or receptors. This review covers traditional theranostics for thyroid cancer and pheochromocytoma with radioiodine compounds. In addition, recent theranostics of radioimmunotherapy for non-Hodgkin lymphoma, and treatment of bone metastasis using bone seeking radiopharmaceuticals are described. Furthermore, new radiopharmaceuticals for prostatic cancer and pancreatic cancer have been added. Of particular, F-18 Fluoro-2-Deoxyglucose (FDG) Positron Emission Tomography (PET) is often used for treatment monitoring and estimating patient outcome. A recent clinical study highlighted the ability of alpha-radiotherapy with high linear energy transfer (LET) to overcome treatment resistance to beta--particle therapy. Theranostics will become an ever-increasing part of clinical nuclear medicine. 相似文献
62.
Makoto Shimizu Takato Kawamura Shinya Fukumoto Isao Mizota Yusong Zhu 《Journal of heterocyclic chemistry》2021,58(3):751-756
The ketene silyl acetal derived from ethyl 2-benzyltetrahydroisoquinoline-1-carboxylate undergoes a rapid oxidation reaction with N-bromosuccinimide to form 3,4-dihydroisoquinolinium ion, which reacts with Grignard reagents to give 1,1-disubstituted tetrahydroisoquinolines in good yields. 相似文献
63.
Kawamura Taiga Wu Hao Kim Seong-Yun 《Journal of Radioanalytical and Nuclear Chemistry》2021,329(2):1001-1009
Journal of Radioanalytical and Nuclear Chemistry - (HDEHP?+?Hexa)/SiO2-P, a silica-based adsorbent, was prepared and used to separate Y(III) from a mixed solution of Sr(II) and Y(III).... 相似文献
64.
Well‐Defined Iron Complexes as Efficient Catalysts for “Green” Atom‐Transfer Radical Polymerization of Styrene,Methyl Methacrylate,and Butyl Acrylate with Low Catalyst Loadings and Catalyst Recycling 下载免费PDF全文
So‐ichiro Nakanishi Dr. Mitsunobu Kawamura Hidetomo Kai Prof. Dr. Ren‐Hua Jin Dr. Yusuke Sunada Prof. Dr. Hideo Nagashima 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(19):5802-5814
Environmentally friendly iron(II) catalysts for atom‐transfer radical polymerization (ATRP) were synthesized by careful selection of the nitrogen substituents of N,N,N‐trialkylated‐1,4,9‐triazacyclononane (R3TACN) ligands. Two types of structures were confirmed by crystallography: “[(R3TACN)FeX2]” complexes with relatively small R groups have ionic and dinuclear structures including a [(R3TACN)Fe(μ‐X)3Fe(R3TACN)]+ moiety, whereas those with more bulky R groups are neutral and mononuclear. The twelve [(R3TACN)FeX2]n complexes that were synthesized were subjected to bulk ATRP of styrene, methyl methacrylate (MMA), and butyl acrylate (BA). Among the iron complexes examined, [{(cyclopentyl)3TACN}FeBr2] ( 4 b ) was the best catalyst for the well‐controlled ATRP of all three monomers. This species allowed easy catalyst separation and recycling, a lowering of the catalyst concentration needed for the reaction, and the absence of additional reducing reagents. The lowest catalyst loading was accomplished in the ATRP of MMA with 4 b (59 ppm of Fe based on the charged monomer). Catalyst recycling in ATRP with low catalyst loadings was also successful. The ATRP of styrene with 4 b (117 ppm Fe atom) was followed by precipitation from methanol to give polystyrene that contained residual iron below the calculated detection limit (0.28 ppm). Mechanisms that involve equilibria between the multinuclear and mononuclear species were also examined. 相似文献
65.
Mapping Platinum Species in Polymer Electrolyte Fuel Cells by Spatially Resolved XAFS Techniques 下载免费PDF全文
Dr. Shinobu Takao Dr. Oki Sekizawa Dr. Shin‐ichi Nagamatsu Dr. Takuma Kaneko Dr. Takashi Yamamoto Dr. Gabor Samjeské Dr. Kotaro Higashi Dr. Kensaku Nagasawa Dr. Takuya Tsuji Dr. Motohiro Suzuki Dr. Naomi Kawamura Dr. Masaichiro Mizumaki Prof. Dr. Tomoya Uruga Prof. Dr. Yasuhiro Iwasawa 《Angewandte Chemie (International ed. in English)》2014,53(51):14110-14114
There is limited information on the mechanism for platinum oxidation and dissolution in Pt/C cathode catalyst layers of polymer electrolyte fuel cells (PEFCs) under the operating conditions though these issues should be uncovered for the development of next‐generation PEFCs. Pt species in Pt/C cathode catalyst layers are mapped by a XAFS (X‐ray absorption fine structure) method and by a quick‐XAFS(QXAFS) method. Information on the site‐preferential oxidation and leaching of Pt cathode nanoparticles around the cathode boundary and the micro‐crack in degraded PEFCs is provided, which is relevant to the origin and mechanism of PEFC degradation. 相似文献
66.
Jianjun Lu Shozo Tokinaga 《The European Physical Journal B - Condensed Matter and Complex Systems》2016,89(10):231
This paper analyses the propagation of the state changes of agents that are induced byexternal forces applied to a plane. In addition, we propose two models for the behavior ofthe agents placed on a lattice plane, both of which are affected by local interactions. Wefirst assume that agents are allowed to move to another site to maximise theirsatisfaction. Second, we utilise a model in which the agents choose activities on eachsite. The results show that the migration (activity) patterns of agents in both modelsachieve stability without any external forces. However, when we apply an impulsiveexternal force to the state of the agents, we then observe the propagation of the changesin the agents’ states. Using simulation studies, we show the conditions for thepropagation of the state changes of the agents. We also show the propagation of the statechanges of the agents allocated in scale-free networks and discuss the estimation of theagents’ decisions in real state changes. Finally, we discuss the estimation of the agents’decisions in real state temporal changes using economic and social data from Japan and theUnited States. 相似文献
67.
68.
Quasi-solid-state dye-sensitized solar cells using room temperature molten salts and a low molecular weight gelator 总被引:1,自引:0,他引:1
Kubo W Kitamura T Hanabusa K Wada Y Yanagida S 《Chemical communications (Cambridge, England)》2002,(4):374-375
A dye-sensitized solar cell fabricated using the room temperature molten salt, 1-hexyl-3-methylimidazolium iodide, iodine and a low molecular weight gelator as a quasisolid-state electrolyte showed a 5.0% light-to-electricity conversion efficiency under AM 1.5 irradiation, and high-temperature stability. 相似文献
69.
Multi-layered thin films, which consisted of metallic silver, GeSe3 glass, and silver oxyhalide superionic conductor glass were prepared. Photo- and electrochemical reaction of metallic silver with the chalcogenide glass layer was studied by optical absorbance and cyclic-voltammetry. Photo-doping of silver through the superionic glass layer was observed using evaporated AgI---Ag2MoO4 film and it was partly undoped by electrochemical treatment. However, no photo-doping was observed for the cell consisting of a AgI---AgPO3 dip-coated layer. The doped silver was dissolved into the GeSe3 layer during the photo-doping process. However, it formed another intermediate compound layer (probably silver selenide) during the electrodoping process. 相似文献
70.
The behavior of arsenite, methylarsonic acid, dimethylarsinic acid, trimethylarsine oxide, dimethyl-R-arsine oxides, and trimethyl-R-arsonium compounds (R = carboxymethyl, 2-carboxyethyl, 2-hydroxyethyl) toward sodium borohydride and hot aqueous sodium hydroxide was investigated. The arsines obtained by sodium borohydride reduction of the undigested and digested solutions were collected in a liquid-nitrogen cooled trap, separated with a gas chromatograph, and detected with a mass spectrometer in the selected-ion-monitoring mode. The investigated arsenic compounds were stable in hot 2 mol dm?3 sodium hydroxide except arsenobetaine [trimethyl(carboxymethyl)arsonium zwitterion] that was converted to trimethylarsine oxide, and dimethyl(ribosyl)arsine oxides that were decomposed to dimethylarsinic acid. Hydride generation before and after digestion of extracts from marine organisms allowed inorganic arsenic, methylated arsenic, arsenobetaine, and ribosyl arsenic compounds to be identified and quantified. This method was applied to extracts from shellfish, fish, crustaceans, and seaweeds. 相似文献