The Foundations of the Development of Technologies of the Synthesis of Radiopharmaceuticals / M. Larkina, E. V. Podrezova, O. Bragina [et al.]

Уровень набора: (RuTPU)RU\TPU\network\4816, AIP Conference ProceedingsАльтернативный автор-лицо: Larkina, M. S., pharmacist, Researcher of the Tomsk Polytechnic University, Candidate of Pharmaceutical Sciences, 1984-, Mariya Sergeevna;Podrezova, E. V., Chemist, Engineer of Tomsk Polytechnic University, 1992-, Ekaterina Vladimirovna;Bragina, O. D., specialist in the field of medical technology, Associate Scientist of Tomsk Polytechnic University, Candidate of medical Sciences, 1986-, Olga Dmitrievna;Stasyuk, E. S., Specialist in the field of nuclear power engineering, Researcher of Tomsk Polytechnic University, Candidate of technical sciences, 1978-, Elena Sergeyevna;Yusubov, M. S., chemist, Professor of Tomsk Polytechnic University, Doctor of chemical sciences, 1961-, Mekhman Suleiman-Ogly (Suleimanovich);Chernov, V. I., specialist in the field of medical technology, lead engineer of Tomsk Polytechnic University, doctor of medical sciences, 1962-, Vladimir Ivanovich;Zelchan, R. V., specialist in the field of medical technology, laboratory Tomsk Polytechnic University, 1984-, Roman Vladimirovich;Skuridin, V. S., Physicist, Specialist in the field of nuclear power engineering, Professor of Tomsk Polytechnic University, Doctor of technical sciences, 1946-, Viktor Sergeyevich;Belousov, M.;Deev, S. M., biologist, the expert of Tomsk Polytechnic University, doctor of biological Sciences, Sergey MikhaylovichКоллективный автор (вторичный): Национальный исследовательский Томский политехнический университет (ТПУ), Институт природных ресурсов (ИПР), Кафедра технологии органических веществ и полимерных материалов (ТОВПМ);Национальный исследовательский Томский политехнический университет (ТПУ), Физико-технический институт (ФТИ), Лаборатория № 31 ядерного реактора (Лаборатория № 31 ЯР);Национальный исследовательский Томский политехнический университет, Исследовательская школа химических и биомедицинских технологий (ИШХБМТ), (2017- )Язык: английский.Резюме или реферат: The selection of precursors (for example chelating agents) and development of a technique of chemical modification of the target molecules retaining its ability to bind to specific receptors are very important in the synthesis of radiopharmaceuticals. As some important precursors for target radiopharmaceuticals omega-iodo-aliphatic carboxylic acids and their esters can be used. We have developed an environmentally safe process for producing omega-iodoaliphatic carboxylic acids and their esters of the available, inexpensive and low toxic aliphatic cyclic ketones. We proposed a new method for the synthesis of the chelating agents omega-thia- or (bis(2-hydroxyethyl)amino)- aliphatic carboxylic acids (chelate 1 and chelate 2), which was caused by the existing disadvantages in the existing methods. Thus, based on our method the precursors (chelates) with yield of over 70-90% on the final stage were synthesized, and then the high effectiveness in producing target radiopharmaceuticals using different biomolecules was showed. 99mTc-chelates complexes were prepared with radiochemical purity >91% and found to be stable at room temperature for six hours..Примечания о наличии в документе библиографии/указателя: [References: 15 tit.].Аудитория: .Тематика: электронный ресурс | труды учёных ТПУ | синтез | радиофармпрепараты | мишени | ядерная медицина | радионуклиды | терапия Ресурсы он-лайн:Щелкните здесь для доступа в онлайн | Щелкните здесь для доступа в онлайн
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[References: 15 tit.]

The selection of precursors (for example chelating agents) and development of a technique of chemical modification of the target molecules retaining its ability to bind to specific receptors are very important in the synthesis of radiopharmaceuticals. As some important precursors for target radiopharmaceuticals omega-iodo-aliphatic carboxylic acids and their esters can be used. We have developed an environmentally safe process for producing omega-iodoaliphatic carboxylic acids and their esters of the available, inexpensive and low toxic aliphatic cyclic ketones. We proposed a new method for the synthesis of the chelating agents omega-thia- or (bis(2-hydroxyethyl)amino)- aliphatic carboxylic acids (chelate 1 and chelate 2), which was caused by the existing disadvantages in the existing methods. Thus, based on our method the precursors (chelates) with yield of over 70-90% on the final stage were synthesized, and then the high effectiveness in producing target radiopharmaceuticals using different biomolecules was showed. 99mTc-chelates complexes were prepared with radiochemical purity >91% and found to be stable at room temperature for six hours.

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