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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">zldm</journal-id><journal-title-group><journal-title xml:lang="ru">Заводская лаборатория. Диагностика материалов</journal-title><trans-title-group xml:lang="en"><trans-title>Industrial laboratory. Diagnostics of materials</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1028-6861</issn><issn pub-type="epub">2588-0187</issn><publisher><publisher-name>ООО «Издательство «ТЕСТ-ЗЛ»</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.26896/1028-6861-2019-85-9-5-14</article-id><article-id custom-type="elpub" pub-id-type="custom">zldm-1055</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>АНАЛИЗ ВЕЩЕСТВА</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>SUBSTANCES ANALYSIS</subject></subj-group></article-categories><title-group><article-title>Модифицированные твердоконтактные сенсоры для определения цефуроксима и цефалексина в лекарственных средствах и ротовой жидкости</article-title><trans-title-group xml:lang="en"><trans-title>Modified solid-contact sensors for determination of cefuroxime and cefalexin in medicines and oral fluid</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>Кулапина</surname><given-names>Е. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Kulapina</surname><given-names>E. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кулапина Елена Григорьевна </p><p>410012, г. Саратов, ул. Астраханская, 83</p></bio><bio xml:lang="en"><p> Elena G. Kulapina</p><p>83 Astrakhanskaya st., Saratov, 410012</p></bio><email xlink:type="simple">kulapinaeg@mail.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>Дубасова</surname><given-names>А. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Dubasova</surname><given-names>A. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Дубасова Анастасия Евгеньевна </p><p>410012, г. Саратов, ул. Астраханская, 83</p></bio><bio xml:lang="en"><p> Anastasia E. Dubasova</p><p>83 Astrakhanskaya st., Saratov, 410012</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кулапина</surname><given-names>О. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Kulapina</surname><given-names>O. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кулапина Ольга Ивановна </p><p>410012, г. Саратов, ул. Боль¬шая Казачья, 112</p></bio><bio xml:lang="en"><p>Olga I. Kulapina</p><p>112 Bol’shaya Kazach’ya st., Saratov, 410012</p></bio><email xlink:type="simple">olgakulapina@mail.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Саратовский национальный исследовательский государственный университет им. Н. Г. Чернышевского</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Saratov State University, Department of Chemistry</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Саратовский государственный медицинский университет им. В. И. Разумовского</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Saratov State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>23</day><month>09</month><year>2019</year></pub-date><volume>85</volume><issue>9</issue><fpage>5</fpage><lpage>14</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Кулапина Е.Г., Дубасова А.Е., Кулапина О.И., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Кулапина Е.Г., Дубасова А.Е., Кулапина О.И.</copyright-holder><copyright-holder xml:lang="en">Kulapina E.G., Dubasova A.E., Kulapina O.I.</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.zldm.ru/jour/article/view/1055">https://www.zldm.ru/jour/article/view/1055</self-uri><abstract><p>Цефуроксим и цефалексин — цефалоспориновые антибиотики широкого спектра действия. Для их определения в различных объектах используют спектроскопические, хроматографические, электрохимические, иммуноферментные и другие методы, которые требуют применения дорогостоящей аппаратуры и органических растворителей. Потенциометрические сенсоры позволяют экспрессно детектировать цефалоспориновые антибиотики в малых объемах проб, без предварительной пробоподготовки. Предложены модифицированные твердоконтактные потенциометрические сенсоры для определения цефуроксима и цефалексина в водных, биологических средах и фармацевтических препаратах. В качестве активных компонентов мембран использовали соединение тетрадециламмония (ТДА) с комплексом серебро (I) — цефуроксим (Ag(Cefur)2); модификаторы — полианилин и наночастицы оксида меди. Определены основные электроаналитические и операционные характеристики исследуемых сенсоров в водных растворах антибиотиков и на фоне жидкости ротовой полости (ЖРП). Исследуемые сенсоры на основе Ag(Cefur)2iyi,A характеризуются небольшим временем отклика: для модифицированных полианилином и наночастицами оксида меди — в пределах 5 - 10 с, для немодифицированных — 10-20 с. Линейный диапазон электродных функций сенсоров в растворах антибиотиков составляет 1 • Ю-4 - 1 • Ю-1 моль/л, предел обнаружения — 7,4 • 10~5 моль/л для немодифицированных и 6,3 • Ю-5 моль/л для модифицированных сенсоров. Дрейф потенциала составляет 6 - 12 и 4-6 мВ/сут, срок службы — 1,5 и 2 мес. для немодифицированных и модифицированных сенсоров соответственно. Модификаторы стабилизируют электродный потенциал и выполняют функцию медиатора электронного переноса, что приводит к улучшению электроаналитических характеристик сенсоров. Выявлено влияние окислительно-восстановительных агентов на свойства сенсоров: 1 • 10~3 - 1 • Ю-4 М растворы К2Сг207 и FeCl3 уменьшают интервалы линейности электродных функций, KI и соль Мора не влияют на характеристики сенсоров в растворах цефуроксима и цефалексина. Коэффициенты потенциометрической селективности модифицированных наночастицами СиО цефуроксим-селективных сенсоров по отношению к цефазолину, цефотаксиму и цефалексину близки к единице; Kfot по отношению к неорганическим анионам, входящим в состав ротовой жидкости (СП, Вг~, 1 ,НСОд,HgPO^,НРО|~), составляют п • Ю-2 - п • Ю-3. Это свидетельствует о возможности применения сенсоров для определения индивидуальных цефалоспориновых антибиотиков или их суммарного содержания в присутствии 100 - 1000-кратных избытков неорганических ионов в лекарственных и биологических средах, малых объемах проб, что важно при исследовании фармакокинетики антибиотиков, определения максимальной терапевтической дозы, корректировки процесса лечения. </p></abstract><trans-abstract xml:lang="en"><p>Cefuroxime, cefuroxime axetil and cefalexin are broad-spectrum pluripotential cephalosporin antibiotics. Their determination in various objects suggests using expensive spectroscopic, chromatographic, electrochemical equipment and organic solvents. Potentiometric sensors can provide rapid detection of cephalosporin antibiotics in a small sample volume without a preliminary sample preparation. The study is aimed at the developing of modified solid-contact potentiometric sensors for determination of cefuroxime and cefalexin in aqueous, biological media, and pharmaceuticals. The electroanalytical characteristics of unmodified and modified polyaniline and copper oxide nanoparticle sensors are evaluated. Tetradecylammonium(TDA) with a silver (I) – cefuroxime complex are used as the active membrane components, whereas polyaniline and copper oxide nanoparticles are used as modifiers. The main electroanalytic and operational characteristics of the studied sensors in aqueous solutions of antibiotics and against the background of oral fluid (LRP) are determined. The results of comparative evaluation of the electroanalytical properties of unmodified and modified solid-contact sensors in aqueous media of some â-lactam antibiotics and against the background of oral fluid are presented. The sensors based on Ag (Cefur)2TDA are characterized by a short response time: for modified polyaniline (PAN) and copper oxide nanoparticles within 5 – 10 sec, for unmodified — 10 – 20 sec. The linear range of the electrode functions for unmodified and modified sensors is 1 × 10–4 – 1 × 10–1 M, the detection limit is 7.4 × 10–5 M for unmodified and 6.3 × 10–5 M for modified sensors, respectively. The potential drift is 6 – 12 and 4 – 6 mV/day, service life is 1.5 and 2 months for unmodified and modified sensors, respectively. The modifiers stabilize the electrode potential, perform the function of the electron transfer mediator thus enhancing the electroanalytical characteristics of the sensors. The effect of the redox agents on the sensor properties is revealed: 1 × 10–3 – 1 × 10–4 MK 2Cr2O7 and FeCl3 solutions reduce the linearity intervals of the electrode functions, KI and Mohr’s salt do not affect the characteristics of the sensors in cefuroxime and cephalexin solutions. The coefficients of potentiometric selectivity of cefuroxime-selective sensors (modified with CuO nanoparticles) with respect to cefazolin, cefotaxime, and cefalexin are close to unity; Kijpot with respect to inorganic anions being part of the oral fluid (, Cl Br,I,HCO3 ,H PO 24 ,HPO4 2) are n × 10–2 – n × 10–3. This indicates the possibility of using sensors for detecting individual cephalosporin antibiotics or their total content in the presence of 100 – 1000 fold excesses of inorganic ions in medicinal and biological environments, small sample volumes, which is important when studying the pharmacokinetics of antibiotics and in determination of the maximum therapeutic dose when adjusting the treatment process.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>потенциометрические сенсоры</kwd><kwd>полианилин</kwd><kwd>наночастицы оксида меди</kwd><kwd>цефуроксим</kwd><kwd>цефуроксим аксетил</kwd><kwd>цефалексин</kwd></kwd-group><kwd-group xml:lang="en"><kwd>potentiometric sensors</kwd><kwd>polyaniline</kwd><kwd>copper oxide nanoparticles</kwd><kwd>cefuroxime</kwd><kwd>cefuroxime axetil</kwd><kwd>cefalexin</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">Беликов В. Г. 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