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<article article-type="research-article" dtd-version="1.2" xml:lang="ru" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><front><journal-meta><journal-id journal-id-type="issn">2658-6533</journal-id><journal-title-group><journal-title>Research Results in Biomedicine</journal-title></journal-title-group><issn pub-type="epub">2658-6533</issn></journal-meta><article-meta><article-id pub-id-type="doi">10.18413/2313-8955-2017-3-3-74-81</article-id><article-id pub-id-type="publisher-id">1194</article-id><article-categories><subj-group subj-group-type="heading"><subject>Archive categories</subject></subj-group></article-categories><title-group><article-title>QUANTITATIVE DETERMINATION OF THE INNOVATIVE NEOPIOID ANALGETIC IN A MUKOADAGESIVE DOSAGE FORM</article-title><trans-title-group xml:lang="en"><trans-title>QUANTITATIVE DETERMINATION OF THE INNOVATIVE NEOPIOID ANALGETIC IN A MUKOADAGESIVE DOSAGE FORM</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Avtina</surname><given-names>Tatiana V.</given-names></name><name xml:lang="en"><surname>Avtina</surname><given-names>Tatiana V.</given-names></name></name-alternatives><email>avtina_t@bsu.edu.ru</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Pokrovskii</surname><given-names>Mikhail V.</given-names></name><name xml:lang="en"><surname>Pokrovskii</surname><given-names>Mikhail V.</given-names></name></name-alternatives><email>pokrovskii@bsuedu.ru</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Kulikov</surname><given-names>Aleksandr L.</given-names></name><name xml:lang="en"><surname>Kulikov</surname><given-names>Aleksandr L.</given-names></name></name-alternatives><email>kulikov@bsu.edu.ru</email></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="ru"><surname>Avtina</surname><given-names>Natalia V.</given-names></name><name xml:lang="en"><surname>Avtina</surname><given-names>Natalia V.</given-names></name></name-alternatives></contrib></contrib-group><pub-date pub-type="epub"><year>2017</year></pub-date><volume>3</volume><issue>3</issue><fpage>0</fpage><lpage>0</lpage><self-uri content-type="pdf" xlink:href="/media/medicine/2017/3/74-81.pdf" /><abstract xml:lang="ru"><p>Introduction. The TRPA1 channel blocker (ZC02-0012) is an innovative drug belonging to the class of non-opioid analgesics. According to the results of his pharmacokinetic studies, a decision was made on the expediency of developing its prolonged dosage form, which was chosen as biopolymer films, which are one of the innovative long-acting dosage forms intended for topical application and possessing a number of positive properties. In order to standardize the dosage form in terms of the &amp;quot;Quantitative Content&amp;quot; indicator, there was developed a method using a highly efficient liquid chromatograph with a diode-array detector. Materials and methods. The subject of the study includes biopolymer films containing a non-opioid analgesic, a blocker of TRPA1 channels (ZC02-0012). The quantitative content of the non-opioid analgesic was confirmed by HPLC under the following conditions: instrument &amp;ndash; a liquid chromatograph with a working pressure range of 0-60 mPa; detector is spectrophotometric with a diode array system operating in the range of 195-400 nm; protective column &amp;ndash; Zorbax SB C8 12.5 &amp;times; 4.6 mm with a particle size of 5.0 &amp;mu;m; column &amp;ndash; Zorbax SB C8 150 &amp;times; 4.6 mm with a particle size of 3.5 &amp;mu;m; mobile phase A &amp;ndash; 10.35 g/l KCLO4 + 2.6 ml/l HCLO4; mobile phase B &amp;ndash; acetonitrile; the temperature of the sample thermostat is 5&amp;ordm;C; the temperature of the column thermostat is 40&amp;ordm;C; injection volume &amp;ndash; 20 &amp;mu;l; retention time of ZC02-0012 is about 7.0 minutes; wavelength is 291 nm (190-400 nm for identification); separation mode &amp;ndash; linear gradient elution. The method of quantitative determination of a non-opioid analgesic in a biopolymer film was studied by validation characteristics: specificity, accuracy, linearity and precision. Results and discussion. Validation procedure proved the accuracy, linearity and precision of the method of quantitative determination of a non-opioid analgesic in a biodegradable polymeric film in the concentration range of 80-120% of the nominal content of a pharmacologically active substance. The validation characteristics of the method were obtained: accuracy (er max &amp;ndash; 0.31%, er average &amp;ndash; 0.07%, &amp;Delta;er = 0.04%); linearity (linear dependence of optical density on analgesic concentration is observed, r = 0.99987); precision (Sraverage &amp;ndash; 1.45%, &amp;epsilon;average &amp;ndash; 1.03%). The quantitative content of the non-opioid analgesic in the biopolymer film ranges from 90% to 110%. Conclusion. The developed and validated method for the quantitative determination of the non-opioid analgesic was successfully applied to standardize the biopolymer film ZC02-0012 in terms of the &amp;quot;Quantitative content&amp;quot; indicator.</p></abstract><trans-abstract xml:lang="en"><p>Introduction. The TRPA1 channel blocker (ZC02-0012) is an innovative drug belonging to the class of non-opioid analgesics. According to the results of his pharmacokinetic studies, a decision was made on the expediency of developing its prolonged dosage form, which was chosen as biopolymer films, which are one of the innovative long-acting dosage forms intended for topical application and possessing a number of positive properties. In order to standardize the dosage form in terms of the &amp;quot;Quantitative Content&amp;quot; indicator, there was developed a method using a highly efficient liquid chromatograph with a diode-array detector. Materials and methods. The subject of the study includes biopolymer films containing a non-opioid analgesic, a blocker of TRPA1 channels (ZC02-0012). The quantitative content of the non-opioid analgesic was confirmed by HPLC under the following conditions: instrument &amp;ndash; a liquid chromatograph with a working pressure range of 0-60 mPa; detector is spectrophotometric with a diode array system operating in the range of 195-400 nm; protective column &amp;ndash; Zorbax SB C8 12.5 &amp;times; 4.6 mm with a particle size of 5.0 &amp;mu;m; column &amp;ndash; Zorbax SB C8 150 &amp;times; 4.6 mm with a particle size of 3.5 &amp;mu;m; mobile phase A &amp;ndash; 10.35 g/l KCLO4 + 2.6 ml/l HCLO4; mobile phase B &amp;ndash; acetonitrile; the temperature of the sample thermostat is 5&amp;ordm;C; the temperature of the column thermostat is 40&amp;ordm;C; injection volume &amp;ndash; 20 &amp;mu;l; retention time of ZC02-0012 is about 7.0 minutes; wavelength is 291 nm (190-400 nm for identification); separation mode &amp;ndash; linear gradient elution. The method of quantitative determination of a non-opioid analgesic in a biopolymer film was studied by validation characteristics: specificity, accuracy, linearity and precision. Results and discussion. Validation procedure proved the accuracy, linearity and precision of the method of quantitative determination of a non-opioid analgesic in a biodegradable polymeric film in the concentration range of 80-120% of the nominal content of a pharmacologically active substance. The validation characteristics of the method were obtained: accuracy (er max &amp;ndash; 0.31%, er average &amp;ndash; 0.07%, &amp;Delta;er = 0.04%); linearity (linear dependence of optical density on analgesic concentration is observed, r = 0.99987); precision (Sraverage &amp;ndash; 1.45%, &amp;epsilon;average &amp;ndash; 1.03%). The quantitative content of the non-opioid analgesic in the biopolymer film ranges from 90% to 110%. Conclusion. The developed and validated method for the quantitative determination of the non-opioid analgesic was successfully applied to standardize the biopolymer film ZC02-0012 in terms of the &amp;quot;Quantitative content&amp;quot; indicator.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>polymer film</kwd><kwd>quantitative determination</kwd><kwd>non-opioid analgesic</kwd><kwd>blocker TRPA1 channels</kwd><kwd>high-performance liquid chromatography</kwd></kwd-group><kwd-group xml:lang="en"><kwd>polymer film</kwd><kwd>quantitative determination</kwd><kwd>non-opioid analgesic</kwd><kwd>blocker TRPA1 channels</kwd><kwd>high-performance liquid chromatography</kwd></kwd-group></article-meta></front><back><ref-list><title>Список литературы</title><ref id="B1"><mixed-citation>Lazarev A.I., Chestnikova S.E., Erofeeva L.N., Pankrusheva T.A. Use of polymeric application antibacterial films for the treatment of patients with perforated odontogenic maxillary sinusitis. 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