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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">kurskvest</journal-id><journal-title-group><journal-title xml:lang="ru">Человек и его здоровье</journal-title><trans-title-group xml:lang="en"><trans-title>Humans and their health</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1998-5746</issn><issn pub-type="epub">1998-5754</issn><publisher><publisher-name>Kursk State Medical University</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21626/vestnik/2018-2/15</article-id><article-id custom-type="elpub" pub-id-type="custom">kurskvest-373</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ФАРМАЦЕВТИЧЕСКИЕ НАУКИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PHARMACEUTICAL SCIENCES</subject></subj-group></article-categories><title-group><article-title>Особенности определения 2-диметиламино-1,3-бис-(фенилсульфонилтио)пропана (бенсултапа) в лекарственном растительном сырье</article-title><trans-title-group xml:lang="en"><trans-title>Peculiarities of determining 2-dimethylamine-1.3-bis- (phenylsulphonylthio) propane (bensultap) in vegetable raw materials</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Баранов</surname><given-names>Ю. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Baranov</surname><given-names>Yu. N.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шорманов</surname><given-names>В. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Shormanov</surname><given-names>V. K.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сухомлинов</surname><given-names>Ю. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Sukhomlinov</surname><given-names>Yu. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кучер</surname><given-names>М. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Kucher</surname><given-names>M. M.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Коваленко</surname><given-names>Е. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Kovalenko</surname><given-names>E. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Курский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Kursk State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Львовский национальный медицинский университет имени Данила Галицкого</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Lviv National Medical University named after Danil Galitsky</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>20</day><month>06</month><year>2018</year></pub-date><volume>0</volume><issue>2</issue><fpage>94</fpage><lpage>99</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Баранов Ю.Н., Шорманов В.К., Сухомлинов Ю.А., Кучер М.М., Коваленко Е.А., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Баранов Ю.Н., Шорманов В.К., Сухомлинов Ю.А., Кучер М.М., Коваленко Е.А.</copyright-holder><copyright-holder xml:lang="en">Baranov Y.N., Shormanov V.K., Sukhomlinov Y.A., Kucher M.M., Kovalenko E.A.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.kursk-vestnik.ru/jour/article/view/373">https://www.kursk-vestnik.ru/jour/article/view/373</self-uri><abstract><p>Обоснованы преимущества изолирования анализируемого соединения из надземных и подземных органов лекарственных растений смесью органических растворителей ацетонитрил-дихлорэтан-этилацетат (6:2:2 по объему) путем двукратного настаивания при продолжительности каждого этапа настаивания 30 минут и массовом соотношении изолирующего агента и биоматрицы 4:1. Для очистки извлекаемого из растительных биоматриц 2-диметиламино-1,3-бис-(фенилсульфонилтио)пропана применена макроколоночная адсорбционная хроматография в колонке силикагеля «Merk» 40/63 µ и элюирование последовательно гексаном и системой растворителей диэтиловый эфир-гексан (8:2 по объему). Разработана методика определения 2-диметиламино-1,3-бис-(фенилсульфонилтио)пропана в лекарственном растительном сырье с использованием метода ГХ-МС после предварительной термодеструкции анализируемого соединения. Предел обнаружения 2-диметиламино-1,3-бис-(фенилсульфонилтио)пропана составляет 1,0∙10-4 г в 100 г биоматериала.</p></abstract><trans-abstract xml:lang="en"><p>The advantages of isolating the analyzed compound from aboveground and underground parts of medicinal plants with a mixture of organic solvents acetonitrile-dichloroethane-ethyl acetate (6:2:2 by volume) are substantiated by double infusion with the duration of each infusion stage of 30 minutes and the mass ratio of the isolating agent to the biomatrix of 4:1. To purify 2-dimethylamino-1.3-bis-(phenylsulphonylthio) propane recovered from plant biomatrices, macrocolumnic adsorption chromatography on a 40/63 μ silica gel column and successive elution with hexane and a solvent system of diethyl ether-hexane (8:2 by volume) were used. A procedure was developed for the determination of 2-dimethylamino-1.3-bis (phenylsulphonylthio) propane in medicinal plant raw materials using the GC-MS method after preliminary thermal destruction of the test compound. The detection limit of 2-dimethylamino-1.3-bis-(phenylsulphonylthio) propane is 1.0∙10-4 g in 100 g of biomaterial.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>2-диметиламино-1</kwd><kwd>3-бис-(фенилсульфонилтио)пропан (бенсултап)</kwd><kwd>лекарственные растения</kwd><kwd>изолирование</kwd><kwd>очистка</kwd><kwd>ГХ-МС</kwd><kwd>определение</kwd><kwd>2-dimethylamino-1.3-bis-(phenylsulphonylthio) propane (bensultap)</kwd><kwd>medicinal plants</kwd><kwd>isolation</kwd><kwd>purification</kwd><kwd>GC-MS</kwd><kwd>determination</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Баранов Ю.Н., Шорманов В.К., Коваленко Е.А. 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