<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">pharmjournal</journal-id><journal-title-group><journal-title xml:lang="ru">Разработка и регистрация лекарственных средств</journal-title><trans-title-group xml:lang="en"><trans-title>Drug development &amp; registration</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2305-2066</issn><issn pub-type="epub">2658-5049</issn><publisher><publisher-name>LLC «CPHA»</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">pharmjournal-289</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>ФАРМАЦЕВТИЧЕСКАЯ ТЕХНОЛОГИЯ И НАНОТЕХНОЛОГИИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PHARMACEUTICAL TECHNOLOGY AND NANOTECHNOLOGY</subject></subj-group></article-categories><title-group><article-title>ВЛИЯНИЕ ГИДРОКСИЭТИЛЦЕЛЛЮЛОЗЫ НА ВЫСВОБОЖДЕНИЕ ГЛИБЕНКЛАМИДА ИЗ ТАБЛЕТОК ПРОЛОНГИРОВАННОГО ДЕЙСТВИЯ</article-title><trans-title-group xml:lang="en"><trans-title>EFFECT OF HYDROXYETHYLCELLULOSE ON THE RELEASE OF GLIBENCLAMIDE FROM SUSTAINED RELEASE TABLETS</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>Трофимов</surname><given-names>С. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Trofimov</surname><given-names>S. V.</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>Пятигорский медико-фармацевтический институт - филиал ГБОУ ВПО «Волгоградский государственный медицинский университет» Министерства здравоохранения Российской Федерации</institution></aff><aff xml:lang="en"><institution>Pyatigorsk Medico-Pharmaeutical Institute, departament of State Federal - Funded Educational Institution of Higher Vocational Training Volgograd State Medical University of the Ministry of Health of the Russian Federation</institution></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>09</day><month>01</month><year>2019</year></pub-date><volume>0</volume><issue>3</issue><fpage>52</fpage><lpage>58</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Трофимов С.В., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Трофимов С.В.</copyright-holder><copyright-holder xml:lang="en">Trofimov S.V.</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.pharmjournal.ru/jour/article/view/289">https://www.pharmjournal.ru/jour/article/view/289</self-uri><abstract><p>Приведены практические результаты исследования влияния размера частиц и способа обработки активной субстанции глибенкламида на профиль высвобождения из матричной таблетированной формы пролонгированного действия. Изучено влияние гидроксиэтилцеллюлозы как компонента, используемого для пролонгации высвобождения, а так же как вещества, способного улучшать скорость рас творения и способствовать более полному высвобождению активной субстанции из пролонгированной готовой лекарственной формы.</p></abstract><trans-abstract xml:lang="en"><p>With this study the results of influence particle size distribution and method of modification API on dissolution profile from matrix tablets with sustained release are shown. The effect of Hydroxyethylcellulose, which is used as sustained release agent, also as an excipient, able to improve dissolution speed and maintain more complete release of an API from sustained release formulation, with glibenclamide as an example has been studied.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>гидроксиэтилцеллюлоза</kwd><kwd>глибенкламид</kwd><kwd>растворение</kwd><kwd>пролонгированное высвобождение</kwd></kwd-group><kwd-group xml:lang="en"><kwd>Hydroxyethylcellulose</kwd><kwd>glibenclamide</kwd><kwd>dissolution</kwd><kwd>sustained release</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">K. Wu, J. Li. Formation and characterization of solid dispersions of piroxicam and polyvinylpyrrolidone using spray drying and precipitation with compressed antisolvent // Journal of pharmaceutical sciences. 2009. V. 98(7). P. 2422-2431.</mixed-citation><mixed-citation xml:lang="en">K. Wu, J. Li. Formation and characterization of solid dispersions of piroxicam and polyvinylpyrrolidone using spray drying and precipitation with compressed antisolvent // Journal of pharmaceutical sciences. 2009. V. 98(7). P. 2422-2431.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">S. Kumar, J. Shen, D.J. Burgess. Nano-amorphous spray dried powder to improve oral bioavailability of itraconazole // Journal of Controlled Release. 2014. V. 192. P. 95-102.</mixed-citation><mixed-citation xml:lang="en">S. Kumar, J. Shen, D.J. Burgess. Nano-amorphous spray dried powder to improve oral bioavailability of itraconazole // Journal of Controlled Release. 2014. V. 192. P. 95-102.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">B. Chauhan, S. Shimpi, A. Padarkar. Preparation and evaluation of glibenclamide-polyglycolized glycerides solid dispersions with silicon dioxide by spray drying technique // European Journal of Pharmaceutical Sciences. 2005. V. 26(2). P. 219-230.</mixed-citation><mixed-citation xml:lang="en">B. Chauhan, S. Shimpi, A. Padarkar. Preparation and evaluation of glibenclamide-polyglycolized glycerides solid dispersions with silicon dioxide by spray drying technique // European Journal of Pharmaceutical Sciences. 2005. V. 26(2). P. 219-230.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">E. Gue, S. Muschert, J.F. Willart, F. Danede, M. Descamps, E. Delcourt-Debruyne, J. Siepmann. Accelerated fenofibrate release from spray-dried microparticles based on polymer blends // Journal of drug delivery science and technology. 2014. V. 24(2). P. 185-190.</mixed-citation><mixed-citation xml:lang="en">E. Gue, S. Muschert, J.F. Willart, F. Danede, M. Descamps, E. Delcourt-Debruyne, J. Siepmann. Accelerated fenofibrate release from spray-dried microparticles based on polymer blends // Journal of drug delivery science and technology. 2014. V. 24(2). P. 185-190.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">J. Fu, L. Xu, X. Wang, S. Zhang, X. Tao, X. Zhao, H. He, X. Tang. Nimodipine (NM) tablets with high dissolution containing NM solid dispersions prepared by hot-melt extrusion // Drug Development and Industrial Pharmacy. 2011. V. 37(8). P. 934-944.</mixed-citation><mixed-citation xml:lang="en">J. Fu, L. Xu, X. Wang, S. Zhang, X. Tao, X. Zhao, H. He, X. Tang. Nimodipine (NM) tablets with high dissolution containing NM solid dispersions prepared by hot-melt extrusion // Drug Development and Industrial Pharmacy. 2011. V. 37(8). P. 934-944.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">R.K. Rajeswari, K. Abbulu, M. Sudhakar. Development, characterization and solubility study of solid dispersion of Valsartan // Journal of Chemical and Pharmaceutical Research. 2014. V. 3(1). P. 180-187.</mixed-citation><mixed-citation xml:lang="en">R.K. Rajeswari, K. Abbulu, M. Sudhakar. Development, characterization and solubility study of solid dispersion of Valsartan // Journal of Chemical and Pharmaceutical Research. 2014. V. 3(1). P. 180-187.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">D.S. Johes, D.N. Margetson, M.S. McAllister, Y. Tao, S. Li, C.P. McCoy, G.P. Andrews. Thermodynamically stable amorphous drug dispersions in amorphous hydrophilic polymers engineered by hot melt extrusion // Chemical Engineering Research and Design. 2014. V. 92(12). P. 3046-3054.</mixed-citation><mixed-citation xml:lang="en">D.S. Johes, D.N. Margetson, M.S. McAllister, Y. Tao, S. Li, C.P. McCoy, G.P. Andrews. Thermodynamically stable amorphous drug dispersions in amorphous hydrophilic polymers engineered by hot melt extrusion // Chemical Engineering Research and Design. 2014. V. 92(12). P. 3046-3054.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">P.C. Senapati, S.K. Sahoo, A.N. Sahu. Mixed surfactant based (SNEDDS) self-nanoemulsifying drug delivery system presenting efavirenz for enhancement of oral bioavailability // Biomedicine &amp; Pharmacotherapy. 2016. V. 80. P. 42-51.</mixed-citation><mixed-citation xml:lang="en">P.C. Senapati, S.K. Sahoo, A.N. Sahu. Mixed surfactant based (SNEDDS) self-nanoemulsifying drug delivery system presenting efavirenz for enhancement of oral bioavailability // Biomedicine &amp; Pharmacotherapy. 2016. V. 80. P. 42-51.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">U. Paaver, V. Matto, P. Veski. Effect of non-ionic surfactants on the dissolution of poorly soluble drugs // European journal of pharmaceutical sciences. 2007. V. 32(1). P. 34-35.</mixed-citation><mixed-citation xml:lang="en">U. Paaver, V. Matto, P. Veski. Effect of non-ionic surfactants on the dissolution of poorly soluble drugs // European journal of pharmaceutical sciences. 2007. V. 32(1). P. 34-35.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">C. Maderuelo, A. Zarzuelo, J. M. Lanao. Critical factors in the release of drugs from sustained release hydrophilic matrices // Journal of Controlled Release. 2011. V. 154. P. 2-19.</mixed-citation><mixed-citation xml:lang="en">C. Maderuelo, A. Zarzuelo, J. M. Lanao. Critical factors in the release of drugs from sustained release hydrophilic matrices // Journal of Controlled Release. 2011. V. 154. P. 2-19.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">L. Yang, R. Fassihi. Examination of drug solubility, polymer types, hydrodynamics and loading dose on drug release behavior from a triple-layer asymmetric configuration delivery system // International Journal of Pharmaceutics. 1997. V. 155. P. 219-229.</mixed-citation><mixed-citation xml:lang="en">L. Yang, R. Fassihi. Examination of drug solubility, polymer types, hydrodynamics and loading dose on drug release behavior from a triple-layer asymmetric configuration delivery system // International Journal of Pharmaceutics. 1997. V. 155. P. 219-229.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">S. Ensslin, K.P. Moll, K. Paulus, K. Mader. New insight into modified release pellets - Internal structure and drug release mechanism // Journal of Controlled Release. 2008. V. 128. P. 149-156.</mixed-citation><mixed-citation xml:lang="en">S. Ensslin, K.P. Moll, K. Paulus, K. Mader. New insight into modified release pellets - Internal structure and drug release mechanism // Journal of Controlled Release. 2008. V. 128. P. 149-156.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">S. Conti, L. Maggi, L. Segale, E. Ochoa Machiste, U. Conte, P. Grenier, G. Vergnault. Matrices containing NaCMC and HPMC. Swelling and release mechanism study// International Journal of Pharmaceutics 2007. V. 333. P. 143-151.</mixed-citation><mixed-citation xml:lang="en">S. Conti, L. Maggi, L. Segale, E. Ochoa Machiste, U. Conte, P. Grenier, G. Vergnault. Matrices containing NaCMC and HPMC. Swelling and release mechanism study// International Journal of Pharmaceutics 2007. V. 333. P. 143-151.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">D.S. Roy, B.D. Rohera. Comparative evaluation of rate of hydration and matrix erosion of HEC and HPC and study of drug release from their matrices // European Journal of Pharmaceutical Sciences. 2002. V. 16. P. 193-199.</mixed-citation><mixed-citation xml:lang="en">D.S. Roy, B.D. Rohera. Comparative evaluation of rate of hydration and matrix erosion of HEC and HPC and study of drug release from their matrices // European Journal of Pharmaceutical Sciences. 2002. V. 16. P. 193-199.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">S. Yalkowsky, S.C. Valvani. Solubility and Partitioning. I: Solubility of Nonelectrolytes in Water // Journal of Pharmaceutical Sciences. 1980. V. 69(8). P. 912-922.</mixed-citation><mixed-citation xml:lang="en">S. Yalkowsky, S.C. Valvani. Solubility and Partitioning. I: Solubility of Nonelectrolytes in Water // Journal of Pharmaceutical Sciences. 1980. V. 69(8). P. 912-922.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">http://www.drugbank.ca/drugs/DB01016 (дата обращения 04.03.2016).</mixed-citation><mixed-citation xml:lang="en">http://www.drugbank.ca/drugs/DB01016 (дата обращения 04.03.2016).</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Analytical profiles of drug substances: Glibenclamide / Ed. by Klaus Florey. - New Jersey: Academic Press. 1981. 727 p.</mixed-citation><mixed-citation xml:lang="en">Analytical profiles of drug substances: Glibenclamide / Ed. by Klaus Florey. - New Jersey: Academic Press. 1981. 727 p.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Z.H. Loh, A.K. Samanta, P.W.S. Heng. Overview of milling techniques for improving the solubility of poorly water-soluble drugs // Asian journal of pharmaceutical sciences. 2015. V. 10. P. 255-274.</mixed-citation><mixed-citation xml:lang="en">Z.H. Loh, A.K. Samanta, P.W.S. Heng. Overview of milling techniques for improving the solubility of poorly water-soluble drugs // Asian journal of pharmaceutical sciences. 2015. V. 10. P. 255-274.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">P. Khadka, J. Ro, H. Kim, I. Kim, J. T. Kim, Hyunil Kim, J.M. Cho, G. Yun, J. Lee. Pharmaceutical particle technologies: An approach to improve drug solubility, dissolution and bioavailability // Asian journal of pharmaceutical sciences. 2014. V. 9. P. 304-316.</mixed-citation><mixed-citation xml:lang="en">P. Khadka, J. Ro, H. Kim, I. Kim, J. T. Kim, Hyunil Kim, J.M. Cho, G. Yun, J. Lee. Pharmaceutical particle technologies: An approach to improve drug solubility, dissolution and bioavailability // Asian journal of pharmaceutical sciences. 2014. V. 9. P. 304-316.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">J. Lee, J.Y. Choi, C.H. Park. Characteristics of polymers enabling nano-comminution of water-insoluble drugs // International journal of pharmaceutics. 2008. V. 355. P. 328-336.</mixed-citation><mixed-citation xml:lang="en">J. Lee, J.Y. Choi, C.H. Park. Characteristics of polymers enabling nano-comminution of water-insoluble drugs // International journal of pharmaceutics. 2008. V. 355. P. 328-336.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">R. Chen, C. Yi, H. Wu, S. Guo. Degradation kinetics and molecular structure development of hydroxyethyl cellulose under the solid state mechanochemical treatment // Carbohydrate Polymers. 2010. V. 81. P. 188-195.</mixed-citation><mixed-citation xml:lang="en">R. Chen, C. Yi, H. Wu, S. Guo. Degradation kinetics and molecular structure development of hydroxyethyl cellulose under the solid state mechanochemical treatment // Carbohydrate Polymers. 2010. V. 81. P. 188-195.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">ОФС 1.4.1.0015.15. Таблетки // Государственная фармакопея Российской Федерации. 13-е изд. - М., 2015.</mixed-citation><mixed-citation xml:lang="en">ОФС 1.4.1.0015.15. Таблетки // Государственная фармакопея Российской Федерации. 13-е изд. - М., 2015.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">ОФС 1.4.2.0014.15. Растворение для твердых дозированных лекарственных форм // Государственная фармакопея Российской Федерации. 13-е изд. - М., 2015.</mixed-citation><mixed-citation xml:lang="en">ОФС 1.4.2.0014.15. Растворение для твердых дозированных лекарственных форм // Государственная фармакопея Российской Федерации. 13-е изд. - М., 2015.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">H. Liu, L.S. Taylor, K.J. Edgar. The role of polymers in oral bioavailability enhancement: a review // Polymer. 2015. V. 77. P. 399-415.</mixed-citation><mixed-citation xml:lang="en">H. Liu, L.S. Taylor, K.J. Edgar. The role of polymers in oral bioavailability enhancement: a review // Polymer. 2015. V. 77. P. 399-415.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">N.S. Abbas, M. Amin, M.A. Hussain, K.J. Edgar, M.N. Tahir, W. Tremel. Extended release and enhanced bioavailability of moxifloxacin conjugated with hydrophilic cellulose ethers // Carbohydrate Polymers. 2016. V. 136. P. 1297-1306.</mixed-citation><mixed-citation xml:lang="en">N.S. Abbas, M. Amin, M.A. Hussain, K.J. Edgar, M.N. Tahir, W. Tremel. Extended release and enhanced bioavailability of moxifloxacin conjugated with hydrophilic cellulose ethers // Carbohydrate Polymers. 2016. V. 136. P. 1297-1306.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">W.H. De Jong, P.J.A. Borm. Drug delivery and nano- particles: Applications and hazards // International journal of nanomedicine. 2008. V. 3(2). P. 133-149.</mixed-citation><mixed-citation xml:lang="en">W.H. De Jong, P.J.A. Borm. Drug delivery and nano- particles: Applications and hazards // International journal of nanomedicine. 2008. V. 3(2). P. 133-149.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">K. Mitchell, J.L. Ford, D.J. Armstrong, P.N.C. Elliott, J.E. Hogan, C. Rostron. The influence of the particle size of hydroxypropylmethylcellulose K15M on its hydration and performance in matrix tablets // International Journal of Pharmaceutics, 1993. V. 100. P. 175-179.</mixed-citation><mixed-citation xml:lang="en">K. Mitchell, J.L. Ford, D.J. Armstrong, P.N.C. Elliott, J.E. Hogan, C. Rostron. The influence of the particle size of hydroxypropylmethylcellulose K15M on its hydration and performance in matrix tablets // International Journal of Pharmaceutics, 1993. V. 100. P. 175-179.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">P.W.S. Heng, L.W. Chan, M.G. Easterbrook, X. Li. Investigation of the influence of mean HPMC particle size and number of polymer particles on the release of aspirin from swellable hydrophilic matrix tablets // Journal of Controlled Release. 2001. V. 76. P. 39-49.</mixed-citation><mixed-citation xml:lang="en">P.W.S. Heng, L.W. Chan, M.G. Easterbrook, X. Li. Investigation of the influence of mean HPMC particle size and number of polymer particles on the release of aspirin from swellable hydrophilic matrix tablets // Journal of Controlled Release. 2001. V. 76. P. 39-49.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">M.V. Velasco, J.L. Ford, P. Rowe, A.R. Rajabi-Siahboomi. Influence of drug: hydroxypropylmethylcellulose ratio, drug and polymer particle size and compression force on the release of diclofenac sodium from HPMC tablets // Journal of Controlled Release. 1999. V. 57. P. 75-85.</mixed-citation><mixed-citation xml:lang="en">M.V. Velasco, J.L. Ford, P. Rowe, A.R. Rajabi-Siahboomi. Influence of drug: hydroxypropylmethylcellulose ratio, drug and polymer particle size and compression force on the release of diclofenac sodium from HPMC tablets // Journal of Controlled Release. 1999. V. 57. P. 75-85.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">C. Eapen, V.G. Prasanth, A. Rai. Development of UV Spectrometric Method of Glibenclamide (Glyburide) in Bulk and Pharmaceutical Formulations // International Journal of ChemTech Research. 2012. V. 4(1). P. 356-360.</mixed-citation><mixed-citation xml:lang="en">C. Eapen, V.G. Prasanth, A. Rai. Development of UV Spectrometric Method of Glibenclamide (Glyburide) in Bulk and Pharmaceutical Formulations // International Journal of ChemTech Research. 2012. V. 4(1). P. 356-360.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">V.V. Karkhanis, A.D. Captain, P.H. Patel. Development and Validation of UV Spectrophotometric method for estimation of Glibenclamide in bulk and Pharmaceutical dosage forms // Journal of Pharmacy Research Biomed Rx. 2013. V. 1(1). P. 1-3.</mixed-citation><mixed-citation xml:lang="en">V.V. Karkhanis, A.D. Captain, P.H. Patel. Development and Validation of UV Spectrophotometric method for estimation of Glibenclamide in bulk and Pharmaceutical dosage forms // Journal of Pharmacy Research Biomed Rx. 2013. V. 1(1). P. 1-3.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">НД 42-3120-05. Манинил 3,5 мг. 2005.</mixed-citation><mixed-citation xml:lang="en">НД 42-3120-05. Манинил 3,5 мг. 2005.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">The Unired States Pharmacopeial Convention. USP 36 NF-31.2013.</mixed-citation><mixed-citation xml:lang="en">The Unired States Pharmacopeial Convention. USP 36 NF-31.2013.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">E. Aparecida dos Santos Gianotto, R. Pires Arantes, M.J. Lara-Filho, A.C. Saraiva. Casimiro Filho, M.M. Fregonezi-Nery. Dissolution test for glibenclamide tablets // Quimica Nova. 2007. V. 30(5). P. 1218-1221.</mixed-citation><mixed-citation xml:lang="en">E. Aparecida dos Santos Gianotto, R. Pires Arantes, M.J. Lara-Filho, A.C. Saraiva. Casimiro Filho, M.M. Fregonezi-Nery. Dissolution test for glibenclamide tablets // Quimica Nova. 2007. V. 30(5). P. 1218-1221.</mixed-citation></citation-alternatives></ref></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>
