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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">zhps</journal-id><journal-title-group><journal-title xml:lang="ru">Журнал прикладной спектроскопии</journal-title><trans-title-group xml:lang="en"><trans-title>Zhurnal Prikladnoii Spektroskopii</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0514-7506</issn><publisher><publisher-name>B. I. Stepanov Institute of Physics of the National Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">zhps-211</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>***</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>***</subject></subj-group></article-categories><title-group><article-title>БЫСТРОЕ ОБНАРУЖЕНИЕ ТЕТРОДОТОКСИНА С ИСПОЛЬЗОВАНИЕМ СПЕКТРОСКОПИИ ГИГАНТСКОГО КОМБИНАЦИОННОГО РАССЕЯНИЯ И Fe3O4/SiO2/Au ЗОЛОТЫХ/МАГНИТНЫХ НАНОЧАСТИЦ</article-title><trans-title-group xml:lang="en"><trans-title>RAPID DETECTION OF TETRODOTOXIN USING SURFACE-ENHANCED RAMAN SPECTROSCOPY AND Fe3O4/SiO2/Au GOLD/MAGNETIC NANOPARTICLES</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>Neng</surname><given-names>J. .</given-names></name><name name-style="western" xml:lang="en"><surname>Neng</surname><given-names>J. .</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>Wang</surname><given-names>X. .</given-names></name><name name-style="western" xml:lang="en"><surname>Wang</surname><given-names>X. .</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>Jia</surname><given-names>K. .</given-names></name><name name-style="western" xml:lang="en"><surname>Jia</surname><given-names>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>Sun</surname><given-names>P. .</given-names></name><name name-style="western" xml:lang="en"><surname>Sun</surname><given-names>P. .</given-names></name></name-alternatives><email xlink:type="simple">sun_pl@zjut.edu.cn</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Океанический колледж, Технологический университет Чжэцзян</institution></aff><aff xml:lang="en"><institution>Ocean College, Zhejiang University of Technology</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>10</day><month>03</month><year>2020</year></pub-date><volume>85</volume><issue>1</issue><elocation-id>169(1)-169(7)</elocation-id><permissions><copyright-statement>Copyright &amp;#x00A9; Neng J..., Wang X..., Jia K..., Sun P..., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Neng J..., Wang X..., Jia K..., Sun P...</copyright-holder><copyright-holder xml:lang="en">Neng J..., Wang X..., Jia K..., Sun P...</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://zhps.ejournal.by/jour/article/view/211">https://zhps.ejournal.by/jour/article/view/211</self-uri><abstract><p>Наночастицы Fe3O4 модифицированы тетраэтоксисиланом с образованием наночастиц (НЧ) Fe3O4/SiO2, после чего к ним добавлены 3-аминопропил- и 3-тиолпропил-триэтоксисилан, чтобы внедрить NH2- и SH-группы на поверхность наночастиц Fe3O4/SiO2. Затем на их поверхности дополнительно размещались НЧ Au посредством электростатической адсорбции NH2 и Au-S. В результате получены состоящие из ядра и оболочки стабильные магнитные НЧ Fe3O4/SiO2/Au, которые исследованы методами просвечивающей электронной микроскопии (TEM) и энергодисперсионного рентгеновского анализа. Синтезированные НЧ соединены с тетродотоксин-антителами (Ab) и использованы как КР-активный субстрат (Fe3O4/SiO2/Au-Ab), где в качестве КР-метки выступают меченные родамином B (RhB) тетродотоксин-антитела (Ab-RhB). При соединении этих реагентов с тетродотоксином (TTX) генерируется сандвич-комплекс [Fe3O4/SiO2/Au-Ab···TTX···Ab-RhB], обусловленный специфическими взаимодействиями антиген-антитело. Полученный иммунокомплекс отделяли внешним магнитным полем и концентрировали в точечную гранулу, которая при лазерном воздействии давала сильный сигнал, характерный для RhB. Обнаружено, что логарифм интенсивности сигнала пропорционален концентрации TTX с пределом обнаружения 0.01 мкг/мл и диапазоном линейности детектирования ~0.01-0.5 мкг/мл. Разработанный метод обладает повышенной чувствительностью обнаружения и не требует сложных процедур традиционного центрифугирования, колонного разделения и инкубации, что обеспечивает быстрое обнаружение тетродотоксина. </p></abstract><trans-abstract xml:lang="en"><p>Fe3O4 nanoparticles were first modified with tetraethoxylsilane to form Fe3O4/SiO2 nanoparticles, followed by the addition of 3-aminopropyltriethoxysilane and 3-thiolpropyltriethoxysilane to introduce -NH2 and -SH groups to the surface of Fe3O4/SiO2 nanoparticles. Gold nanoparticles were further assembled on the surface of Fe3O4/SiO2 via the electrostatic adsorption of -NH2 and the Au-S bond to produce stable core-shell Fe3O4/SiO2/Au gold/magnetic nanoparticles. These Fe3O4/SiO2/Au gold/magnetic nanoparticles were characterized by a variety of techniques such as transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX), and afterwards conjugated with tetrodotoxin antibodies (Ab) and used as a Raman active substrate (Fe3O4/SiO2/Au-Ab) with Rhodamine B (RhB)-labeled tetrodotoxin antibody as a Raman reporter (Ab-RhB). Upon mixing these reagents with tetrodotoxin (TTX), a sandwich complex [Fe3O4/SiO2/Au-Ab···TTX···Ab-RhB] was generated due to the specific antibody-antigen interactions. The immunocomplex was subsequently separated by an externally applied magnetic source and concentrated into a pellet point, where the laser interrogation of the pellet produced a strong signal characteristic of RhB. The logarithmic intensity of the signal was found to be proportional to the concentration of TTX with a limit of detection of 0.01µg/mL and a detection linearity range of ~0.01-0.5 µg/mL. The established method eliminates the complicated procedures of traditional centrifuging, column separation, and incubation and achieves a rapid detection of tetrodotoxin with improved detection sensitivity. </p></trans-abstract><kwd-group xml:lang="ru"><kwd>спектроскопия гигантского комбинационного рассеяния</kwd><kwd>быстрое обнаружение</kwd><kwd>тетродотоксин</kwd><kwd>магнитные наночастицы</kwd><kwd>surface-enhanced Raman spectroscopy</kwd><kwd>rapid detection</kwd><kwd>tetrodotoxin</kwd><kwd>magnetic nanoparticles</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">E. P. Ragelis, J. Assoc. Chem., 65, 327-331 (1982).</mixed-citation><mixed-citation xml:lang="en">E. P. Ragelis, J. Assoc. Chem., 65, 327-331 (1982).</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">A. S. May, Chem. 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