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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">scbmt</journal-id><journal-title-group><journal-title xml:lang="ru">БИОМЕДИЦИНА</journal-title><trans-title-group xml:lang="en"><trans-title>Journal Biomed</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2074-5982</issn><issn pub-type="epub">2713-0428</issn><publisher><publisher-name>Scientific center of biomedical technologies of Federal Medical and Biological Agency</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">scbmt-668</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>Статьи</subject></subj-group></article-categories><title-group><article-title>Некоторые вопросы оценки токсичности
генно-инженерных лекарственных препаратов</article-title><trans-title-group xml:lang="en"><trans-title></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>Неугодова</surname><given-names>Н. П.</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>Долгова</surname><given-names>Г. В.</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>Гавриков</surname><given-names>А. В.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Научный центр экспертизы средств медицинского применения Министерства
    здравоохранения и социального обеспечения Российской Федерации, Москва</institution><country>Russian Federation</country></aff><aff xml:lang="ru" id="aff-2"><institution>ЗАО «Мосагроген», Москва</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2011</year></pub-date><pub-date pub-type="epub"><day>13</day><month>02</month><year>2020</year></pub-date><volume>1</volume><issue>3</issue><fpage>98</fpage><lpage>100</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Неугодова Н.П., Долгова Г.В., Гавриков А.В., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Неугодова Н.П., Долгова Г.В., Гавриков А.В.</copyright-holder><copyright-holder xml:lang="en">Неугодова Н.П., Долгова Г.В., Гавриков А.В.</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://journal.scbmt.ru/jour/article/view/668">https://journal.scbmt.ru/jour/article/view/668</self-uri><abstract><p>Лекарственные препараты, полученные с помощью технологии рекомбинантных ДНК, должны
контролироваться по показателю «Аномальная токсичность», но не в испытаниях на животных (in
vivo), а с помощью методик, использующих клеточные культуры или одноклеточные микроорганизмы
и основанных на фундаментальных исследованиях биологии и цитологии.
The drugs obtained with recombinant DNA technology should be controlled to «abnormal toxicity» test,
but not in laboratory animals test (in vivo), and with methods based on fundamental biology and cytology
researches. That is in cell-cultures tests or in microorganisms (bacteria) tests.</p></abstract><kwd-group xml:lang="ru"><kwd>генно-инженерные лекарственные препараты</kwd><kwd>аномальная токсичность</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
