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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">phkinetica</journal-id><journal-title-group><journal-title xml:lang="ru">Фармакокинетика и Фармакодинамика</journal-title><trans-title-group xml:lang="en"><trans-title>Pharmacokinetics and Pharmacodynamics</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2587-7836</issn><issn pub-type="epub">2686-8830</issn><publisher><publisher-name>ООО «Издательство ОКИ»</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">phkinetica-156</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>АКТУАЛЬНЫЙ ОБЗОР</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CURRENT REVIEWS</subject></subj-group></article-categories><title-group><article-title>Факторы, влияющие на биологическую доступность лекарственных препаратов</article-title><trans-title-group xml:lang="en"><trans-title>Factors, effecting on drug bioavailability</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>Бочков</surname><given-names>П. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Bochkov</surname><given-names>P. .</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>Шевченко</surname><given-names>Р. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Shevchenko</surname><given-names>R. .</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>Литвин</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Litvin</surname><given-names>A. .</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>Колыванов</surname><given-names>Г. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Kolyvanov</surname><given-names>G. .</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>Жердев</surname><given-names>Владимир Павлович</given-names></name><name name-style="western" xml:lang="en"><surname>Zherdev</surname><given-names>V. .</given-names></name></name-alternatives><email xlink:type="simple">zherdevpharm@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБНУ «НИИ фармакологии имени В.В. Закусова»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>FSBSI «Zakusov Institute of Pharmacology»</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>09</day><month>04</month><year>2020</year></pub-date><volume>0</volume><issue>1</issue><fpage>12</fpage><lpage>20</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Бочков П.О., Шевченко Р.В., Литвин А.А., Колыванов Г.Б., Жердев В.П., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Бочков П.О., Шевченко Р.В., Литвин А.А., Колыванов Г.Б., Жердев В.П.</copyright-holder><copyright-holder xml:lang="en">Bochkov P..., Shevchenko R..., Litvin A..., Kolyvanov G..., Zherdev 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.pharmacokinetica.ru/jour/article/view/156">https://www.pharmacokinetica.ru/jour/article/view/156</self-uri><abstract><p>Рассматривается влияние таких факторов, как вспомогательное вещество, тип и общий физико-химический характер лекарственной формы, некоторые технологические приемы производства лекарственных форм на биологическую доступность лекарственных препаратов. Влияние перечисленных факторов рассмотрено на примерах препаратов, используемых в медицинской практике.</p></abstract><trans-abstract xml:lang="en"><p>Effects such as excipients, type and general physico-chemical properties of drug form, some of technological manufacturing approaches of the drug forms on bioavailability were consider. Effects of the above-listed factors on the examples used in medical practice were demonstrated.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>фармакокинетика</kwd><kwd>биологическая доступность</kwd><kwd>вспомогательные вещества</kwd><kwd>системы контролируемого высвобождения препарата</kwd><kwd>твёрдые дисперсные системы</kwd><kwd>pharmacokinetics</kwd><kwd>bioavalability</kwd><kwd>excipients</kwd><kwd>drug delivery systems</kwd><kwd>solid dispersion systems</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">Aleeva G.N., Zhuravleva M.V., Khafiz’yanova R.K. The role of excipients in determining the pharmaceutical and therapeutic properties of medicinal agents (Review). Pharm. Chem. J. 2009; 43: 4: 230-234.</mixed-citation><mixed-citation xml:lang="en">Aleeva G.N., Zhuravleva M.V., Khafiz’yanova R.K. The role of excipients in determining the pharmaceutical and therapeutic properties of medicinal agents (Review). Pharm. Chem. J. 2009; 43: 4: 230-234.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Koo O.M.Y. Excipients-Application Challenges and Examples of New Excipients in Advanced Drug Delivery Systems. Am. Pharm. Rev. 2011; 14: 2: 60.</mixed-citation><mixed-citation xml:lang="en">Koo O.M.Y. Excipients-Application Challenges and Examples of New Excipients in Advanced Drug Delivery Systems. Am. Pharm. Rev. 2011; 14: 2: 60.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Almeida H., Amaral M.H., Lobao P. Temperature and pH stimuli-responsive polymers and their applications in controlled and selfregulated drug delivery. J. Appl. Pharm. Sci. 2012; 2: 6: 1-10.</mixed-citation><mixed-citation xml:lang="en">Almeida H., Amaral M.H., Lobao P. Temperature and pH stimuli-responsive polymers and their applications in controlled and selfregulated drug delivery. J. Appl. Pharm. Sci. 2012; 2: 6: 1-10.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Shen L., Zhang X., Liu M., Wang Z. Transferring of red Monascus pigments from nonionic surfactant to hydrophobic ionic liquid by novel microemulsion extraction. Sep. Purif. Technol. 2014; 138: 34-40.</mixed-citation><mixed-citation xml:lang="en">Shen L., Zhang X., Liu M., Wang Z. Transferring of red Monascus pigments from nonionic surfactant to hydrophobic ionic liquid by novel microemulsion extraction. Sep. Purif. Technol. 2014; 138: 34-40.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Vilar G., Tulla-Puche J., Albericio F. Polymers and drug delivery systems Curr. Drug Deliver. 2012; 9: 4: 367-394.</mixed-citation><mixed-citation xml:lang="en">Vilar G., Tulla-Puche J., Albericio F. Polymers and drug delivery systems Curr. Drug Deliver. 2012; 9: 4: 367-394.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Vyas A., Saraf S., Saraf S. Cyclodextrin based novel drug delivery systems J. Inclusion Phenom. Macrocyc. Chem. 2008; 62: 1-2: 23-42.</mixed-citation><mixed-citation xml:lang="en">Vyas A., Saraf S., Saraf S. Cyclodextrin based novel drug delivery systems J. Inclusion Phenom. Macrocyc. Chem. 2008; 62: 1-2: 23-42.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Di Cagno M., Nielsen T.T., Larsen K.L., Kuntsche J., Bauer-Brandl A. ß-Cyclodextrin-dextran polymers for the solubilization of poorly soluble drugs Int. J. Pharm. 2014; 468: 1: 258-263.</mixed-citation><mixed-citation xml:lang="en">Di Cagno M., Nielsen T.T., Larsen K.L., Kuntsche J., Bauer-Brandl A. ß-Cyclodextrin-dextran polymers for the solubilization of poorly soluble drugs Int. J. Pharm. 2014; 468: 1: 258-263.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Sammour O.A., Hammad M.A., Zidan A.S., Mowafy A.G. QbD approach of rapid disintegrating tablets incorporating indomethacin solid dispersion. Pharm. Dev. Technol. 2011; 16: 3: 219-227.</mixed-citation><mixed-citation xml:lang="en">Sammour O.A., Hammad M.A., Zidan A.S., Mowafy A.G. QbD approach of rapid disintegrating tablets incorporating indomethacin solid dispersion. Pharm. Dev. Technol. 2011; 16: 3: 219-227.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Laitinen R., Suihko E., Bjorkqvist M., et al. Perphenazine solid dispersions for orally fast-disintegrating tablets: physical stability and formulation Drug Dev. Ind. Pharm. 2010; 36: 5: 601-613.</mixed-citation><mixed-citation xml:lang="en">Laitinen R., Suihko E., Bjorkqvist M., et al. Perphenazine solid dispersions for orally fast-disintegrating tablets: physical stability and formulation Drug Dev. Ind. Pharm. 2010; 36: 5: 601-613.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Huang Y., Luo X., You X., et al. The preparation and evaluation of water-soluble SKLB610 nanosuspensions with improved bioavailability. AAPS PharmSciTech. 2013; 14: 3: 1236-1243.</mixed-citation><mixed-citation xml:lang="en">Huang Y., Luo X., You X., et al. The preparation and evaluation of water-soluble SKLB610 nanosuspensions with improved bioavailability. AAPS PharmSciTech. 2013; 14: 3: 1236-1243.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Lima Á.A.N., Soares-Sobrinho J.L., Silva J.L., et al. The use of solid dispersion systems in hydrophilic carriers to increase benznidazole solubility J. Pharm. Sci. 2011; 100:6: 2443-2451.</mixed-citation><mixed-citation xml:lang="en">Lima Á.A.N., Soares-Sobrinho J.L., Silva J.L., et al. The use of solid dispersion systems in hydrophilic carriers to increase benznidazole solubility J. Pharm. Sci. 2011; 100:6: 2443-2451.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Shah A., Serajuddin A.T.M. Conversion of solid dispersion prepared by acid-base interaction into free-flowing and tabletable powder by using Neusilin® US2. Int. J. Pharm. 2015; 484: 1: 172-180.</mixed-citation><mixed-citation xml:lang="en">Shah A., Serajuddin A.T.M. Conversion of solid dispersion prepared by acid-base interaction into free-flowing and tabletable powder by using Neusilin® US2. Int. J. Pharm. 2015; 484: 1: 172-180.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Kapse S.V., Gaikwad R.V., Samad A., Devarajan P.V., et al. Self nanoprecipitating preconcentrate of tamoxifen citrate for enhanced bioavailability. Int. J. Pharm. 2012; 429: 1: 104-112.</mixed-citation><mixed-citation xml:lang="en">Kapse S.V., Gaikwad R.V., Samad A., Devarajan P.V., et al. Self nanoprecipitating preconcentrate of tamoxifen citrate for enhanced bioavailability. Int. J. Pharm. 2012; 429: 1: 104-112.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Han M., Yu X., Guo Y., et al. Honokiol nanosuspensions: Preparation, increased oral bioavailability and dramatically enhanced biodistribution in the cardio-cerebro-vascular system. Colloids Surf., B: Biointerfaces. 2014; 116: 114-120.</mixed-citation><mixed-citation xml:lang="en">Han M., Yu X., Guo Y., et al. Honokiol nanosuspensions: Preparation, increased oral bioavailability and dramatically enhanced biodistribution in the cardio-cerebro-vascular system. Colloids Surf., B: Biointerfaces. 2014; 116: 114-120.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Liu Y., Zhang D., Duan C., et al. Studies on pharmacokinetics and tissue distribution of bifendate nanosuspensions for intravenous delivery J. Microencapsulation. 2012; 29: 2: 194-203.</mixed-citation><mixed-citation xml:lang="en">Liu Y., Zhang D., Duan C., et al. Studies on pharmacokinetics and tissue distribution of bifendate nanosuspensions for intravenous delivery J. Microencapsulation. 2012; 29: 2: 194-203.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Ali H.S.M., York P., Ali A.M.A., Blagden N. Hydrocortisone nanosuspensions for ophthalmic delivery: a comparative study between microfluidic nanoprecipitation and wet milling. J. Controlled Release. 2011; 149: 2: 175-181.</mixed-citation><mixed-citation xml:lang="en">Ali H.S.M., York P., Ali A.M.A., Blagden N. Hydrocortisone nanosuspensions for ophthalmic delivery: a comparative study between microfluidic nanoprecipitation and wet milling. J. Controlled Release. 2011; 149: 2: 175-181.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Momoh M.A., Brown S.A., Onunkwo G.C., et al. Effect of Hydrophilic and Hydrophobic Binders on the Physico-Chemical Properties of Sodium salicylate Tablet Formulation J. Pharm. Res. 2012; 5: 4: 2045-2048.</mixed-citation><mixed-citation xml:lang="en">Momoh M.A., Brown S.A., Onunkwo G.C., et al. Effect of Hydrophilic and Hydrophobic Binders on the Physico-Chemical Properties of Sodium salicylate Tablet Formulation J. Pharm. Res. 2012; 5: 4: 2045-2048.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Sarode A.L., Wang P., Obara S., Worthen D.R. Supersaturation, nucleation, and crystal growth during single-and biphasic dissolution of amorphous solid dispersions: Polymer effects and implications for oral bioavailability enhancement of poorly water soluble drugs. Eur. J. Pharm. Biopharm. 2014; 86: 3: 351-360.</mixed-citation><mixed-citation xml:lang="en">Sarode A.L., Wang P., Obara S., Worthen D.R. Supersaturation, nucleation, and crystal growth during single-and biphasic dissolution of amorphous solid dispersions: Polymer effects and implications for oral bioavailability enhancement of poorly water soluble drugs. Eur. J. Pharm. Biopharm. 2014; 86: 3: 351-360.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Six K., Daems T., Hoon J. de, et al. Clinical study of solid dispersions of itraconazole prepared by hot-stage extrusion. Eur. J. Pharm. Sci. 2005; 24: 2: 179-186.</mixed-citation><mixed-citation xml:lang="en">Six K., Daems T., Hoon J. de, et al. Clinical study of solid dispersions of itraconazole prepared by hot-stage extrusion. Eur. J. Pharm. Sci. 2005; 24: 2: 179-186.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Pasut G., Veronese F.M. PEG conjugates in clinical development or use as anticancer agents: an overview. Adv. Drug Deliver. Rev. 2009; 61: 13: 1177-1188.</mixed-citation><mixed-citation xml:lang="en">Pasut G., Veronese F.M. PEG conjugates in clinical development or use as anticancer agents: an overview. Adv. Drug Deliver. Rev. 2009; 61: 13: 1177-1188.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Sanchis J., Canal F., Lucas R., Vicent M.J. Polymer-drug conjugates for novel molecular targets. Nanomedicine. 2010; 5: 6: 915-935.</mixed-citation><mixed-citation xml:lang="en">Sanchis J., Canal F., Lucas R., Vicent M.J. Polymer-drug conjugates for novel molecular targets. Nanomedicine. 2010; 5: 6: 915-935.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Liu C., Desai K.G.H., Liu C. Enhancement of dissolution rate of valdecoxib using solid dispersions with polyethylene glycol 4000. Drug Dev. Ind. Pharm. 2005; 31: 1: 1-10.</mixed-citation><mixed-citation xml:lang="en">Liu C., Desai K.G.H., Liu C. Enhancement of dissolution rate of valdecoxib using solid dispersions with polyethylene glycol 4000. Drug Dev. Ind. Pharm. 2005; 31: 1: 1-10.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Du B., Shen G., Wang D., et al. Development and characterization ofglimepiride nanocrystal formulation and evaluation ofits pharmacokinetic in rats. Drug Deliver. 2013; 20: 1: 25-33.</mixed-citation><mixed-citation xml:lang="en">Du B., Shen G., Wang D., et al. Development and characterization ofglimepiride nanocrystal formulation and evaluation ofits pharmacokinetic in rats. Drug Deliver. 2013; 20: 1: 25-33.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Kim S., Kim J.-H., Jeon O., et al. Engineered polymers for advanced drug delivery. Eur. J. Pharm. Biopharm. 2009; 71: 3: 420-430.</mixed-citation><mixed-citation xml:lang="en">Kim S., Kim J.-H., Jeon O., et al. Engineered polymers for advanced drug delivery. Eur. J. Pharm. Biopharm. 2009; 71: 3: 420-430.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Parveen S., Sahoo S.K. Long circulating chitosan/PEG blended PLGA nanoparticle for tumor drug delivery. Eur. J. Pharm. 2011; 670: 2: 372-383.</mixed-citation><mixed-citation xml:lang="en">Parveen S., Sahoo S.K. Long circulating chitosan/PEG blended PLGA nanoparticle for tumor drug delivery. Eur. J. Pharm. 2011; 670: 2: 372-383.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Amiji M.M. Synthesis of anionic poly (ethylene glycol) derivative for chitosan surface modification in blood-contacting applications. Carbohydr. Polym. 1997; 32: 3: 193-199.</mixed-citation><mixed-citation xml:lang="en">Amiji M.M. Synthesis of anionic poly (ethylene glycol) derivative for chitosan surface modification in blood-contacting applications. Carbohydr. Polym. 1997; 32: 3: 193-199.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Dahan A., Miller J.M., Hoffman A. et al. The solubility-permeability interplay in using cyclodextrins as pharmaceutical solubilizers: mechanistic modeling and application to progesterone. J. Pharm. Sci. 2010; 99: 6: 2739-2749.</mixed-citation><mixed-citation xml:lang="en">Dahan A., Miller J.M., Hoffman A. et al. The solubility-permeability interplay in using cyclodextrins as pharmaceutical solubilizers: mechanistic modeling and application to progesterone. J. Pharm. Sci. 2010; 99: 6: 2739-2749.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Miller J.M., Beig A., Krieg B.J., et al. The solubility-permeability interplay: mechanistic modeling and predictive application of the impact of micellar solubilization on intestinal permeation. Molecular Pharmaceutics. 2011; 8: 5: 1848-1856.</mixed-citation><mixed-citation xml:lang="en">Miller J.M., Beig A., Krieg B.J., et al. The solubility-permeability interplay: mechanistic modeling and predictive application of the impact of micellar solubilization on intestinal permeation. Molecular Pharmaceutics. 2011; 8: 5: 1848-1856.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Beig A., Miller J.M., Dahan A. Accounting for the solubility - permeability interplay in oral formulation development for poor water solubility drugs: the effect of PEG-400 on carbamazepine absorption. Eur. J. Pharm. Biopharm. 2012; 81: 2: 386-391.</mixed-citation><mixed-citation xml:lang="en">Beig A., Miller J.M., Dahan A. Accounting for the solubility - permeability interplay in oral formulation development for poor water solubility drugs: the effect of PEG-400 on carbamazepine absorption. Eur. J. Pharm. Biopharm. 2012; 81: 2: 386-391.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Li Z., Han X., Zhai Y., et al. Critical determinant of intestinal permeability and oral bioavailability of pegylated all trans-retinoic acid prodrug-based nanomicelles: Chain length of poly (ethylene glycol) corona. Colloids Surf., B: Biointerfaces. 2015; 130: 133-140.</mixed-citation><mixed-citation xml:lang="en">Li Z., Han X., Zhai Y., et al. Critical determinant of intestinal permeability and oral bioavailability of pegylated all trans-retinoic acid prodrug-based nanomicelles: Chain length of poly (ethylene glycol) corona. Colloids Surf., B: Biointerfaces. 2015; 130: 133-140.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Hughey J.R., Keen J.M., Miller D.A., et. al. The use of inorganic salts to improve the dissolution characteristics of tablets containing Soluplus®-based solid dispersions. Eur. J. Pharm. Sci. 2013; 48: 4: 758-766.</mixed-citation><mixed-citation xml:lang="en">Hughey J.R., Keen J.M., Miller D.A., et. al. The use of inorganic salts to improve the dissolution characteristics of tablets containing Soluplus®-based solid dispersions. Eur. J. Pharm. Sci. 2013; 48: 4: 758-766.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Soh J.L.P., Grachet M., Whitlock M., Lukas T. Characterization, optimisation and process robustness of a co-processed mannitol for the development of orally disintegrating tablets. Pharm. Dev. Tech. 2013; 18: 1: 172-185.</mixed-citation><mixed-citation xml:lang="en">Soh J.L.P., Grachet M., Whitlock M., Lukas T. Characterization, optimisation and process robustness of a co-processed mannitol for the development of orally disintegrating tablets. Pharm. Dev. Tech. 2013; 18: 1: 172-185.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Marwaha M., Sandhu D., Marwaha R.K. Coprocessing of excipients: a review on excipient development for improved tabletting performance. Int. J. Appl. Pharm. 2010; 2: 3: 41-47.</mixed-citation><mixed-citation xml:lang="en">Marwaha M., Sandhu D., Marwaha R.K. Coprocessing of excipients: a review on excipient development for improved tabletting performance. Int. J. Appl. Pharm. 2010; 2: 3: 41-47.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Shamma R.N., Basha M. A novel polymeric solubilizer for optimization of Carvedilol solid dispersions: Formulation design and effect of method of preparation. Powder Technol. 2013; 237: 406-414.</mixed-citation><mixed-citation xml:lang="en">Shamma R.N., Basha M. A novel polymeric solubilizer for optimization of Carvedilol solid dispersions: Formulation design and effect of method of preparation. Powder Technol. 2013; 237: 406-414.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Giri T.K., Jana P., Sa B. Rapidly disintegrating fast release tablets of diazepam using solid dispersion: development and evaluation J. Sci. Ind. Res. 2008; 67: 6: 436-439.</mixed-citation><mixed-citation xml:lang="en">Giri T.K., Jana P., Sa B. Rapidly disintegrating fast release tablets of diazepam using solid dispersion: development and evaluation J. Sci. Ind. Res. 2008; 67: 6: 436-439.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Goddeeris C., Willems T., Van den Mooter G. Formulation of fast disintegrating tablets of ternary solid dispersions consisting of TPGS 1000 and HPMC 2910 or PVPVA 64 to improve the dissolution of the anti-HIV drug UC 781. Eur. J. Pharm. Sci. 2008; 34: 4: 293-302.</mixed-citation><mixed-citation xml:lang="en">Goddeeris C., Willems T., Van den Mooter G. Formulation of fast disintegrating tablets of ternary solid dispersions consisting of TPGS 1000 and HPMC 2910 or PVPVA 64 to improve the dissolution of the anti-HIV drug UC 781. Eur. J. Pharm. Sci. 2008; 34: 4: 293-302.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Dinunzio J.C., Schilling S. U., Coney A.W., et al. Use of highly compressible Ceolus™ microcrystalline cellulose for improved dosage form properties containing a hydrophilic solid dispersion. Drug Dev. Ind. Pharm. 2012; 38: 2: 180-189.</mixed-citation><mixed-citation xml:lang="en">Dinunzio J.C., Schilling S. U., Coney A.W., et al. Use of highly compressible Ceolus™ microcrystalline cellulose for improved dosage form properties containing a hydrophilic solid dispersion. Drug Dev. Ind. Pharm. 2012; 38: 2: 180-189.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Leane M.M., Sinclair W., Qian F., et al. Formulation and process design for a solid dosage form containing a spray-dried amorphous dispersion of ibipinabant. Pharm. Dev. Tech. 2013; 18: 2: 359-366.</mixed-citation><mixed-citation xml:lang="en">Leane M.M., Sinclair W., Qian F., et al. Formulation and process design for a solid dosage form containing a spray-dried amorphous dispersion of ibipinabant. Pharm. Dev. Tech. 2013; 18: 2: 359-366.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Fu Q., Sun J., Zhang D., et al. Nimodipine nanocrystals for oral bioavailability improvement: Preparation, characterization and pharmacokinetic studies. Colloids Surf., B: Biointerfaces. 2013; 109: 161-166.</mixed-citation><mixed-citation xml:lang="en">Fu Q., Sun J., Zhang D., et al. Nimodipine nanocrystals for oral bioavailability improvement: Preparation, characterization and pharmacokinetic studies. Colloids Surf., B: Biointerfaces. 2013; 109: 161-166.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Hong C., Dang Y., Lin G., et al. Effects of stabilizing agents on the development of myricetin nanosuspension and its characterization: An in vitro and in vivo evaluation. Int. J. Pharm. 2014; 477: 1: 251-260.</mixed-citation><mixed-citation xml:lang="en">Hong C., Dang Y., Lin G., et al. Effects of stabilizing agents on the development of myricetin nanosuspension and its characterization: An in vitro and in vivo evaluation. Int. J. Pharm. 2014; 477: 1: 251-260.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Ige P.P., Baria K., Gattani S. G. Fabrication of fenofibrate nanocrystals by probe sonication method for enhancement of dissolution rate and oral bioavailability. Colloids Surf., B: Biointerfaces. 2013; 108: 366-373.</mixed-citation><mixed-citation xml:lang="en">Ige P.P., Baria K., Gattani S. G. Fabrication of fenofibrate nanocrystals by probe sonication method for enhancement of dissolution rate and oral bioavailability. Colloids Surf., B: Biointerfaces. 2013; 108: 366-373.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Jiang T., Han N., Zhao B., et al. Enhanced dissolution rate and oral bioavailability of simvastatin nanocrystal prepared by sonoprecipitation. Drug Dev. Ind. Pharm. 2012; 38: 10: 1230-1239.</mixed-citation><mixed-citation xml:lang="en">Jiang T., Han N., Zhao B., et al. Enhanced dissolution rate and oral bioavailability of simvastatin nanocrystal prepared by sonoprecipitation. Drug Dev. Ind. Pharm. 2012; 38: 10: 1230-1239.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Di L., Fish P. V., Mano T. Bridging solubility between drug discovery and development. Drug Discovery Today. 2012; 17: 9: 486-495.</mixed-citation><mixed-citation xml:lang="en">Di L., Fish P. V., Mano T. Bridging solubility between drug discovery and development. Drug Discovery Today. 2012; 17: 9: 486-495.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Varshosaz J., Talari R., Mostafavi S.A., Nokhodchi A. Dissolution enhancement of gliclazide using in situ micronization by solvent change method. Powder Technol. 2008; 187: 3: 222-230.</mixed-citation><mixed-citation xml:lang="en">Varshosaz J., Talari R., Mostafavi S.A., Nokhodchi A. Dissolution enhancement of gliclazide using in situ micronization by solvent change method. Powder Technol. 2008; 187: 3: 222-230.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Kawabata Y., Wada K., Nakatani M., et al. Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: basic approaches and practical applications. Int. J. Pharm. 2011; 420: 1: 1-10.</mixed-citation><mixed-citation xml:lang="en">Kawabata Y., Wada K., Nakatani M., et al. Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: basic approaches and practical applications. Int. J. Pharm. 2011; 420: 1: 1-10.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Zeng N., Hu Q., Liu Z., et al. Preparation and characterization of paclitaxel-loaded DSPE-PEG-liquid crystalline nanoparticles (LCNPs) for improved bioavailability. Int. J. Pharm. 2012; 424: 1: 58-66.</mixed-citation><mixed-citation xml:lang="en">Zeng N., Hu Q., Liu Z., et al. Preparation and characterization of paclitaxel-loaded DSPE-PEG-liquid crystalline nanoparticles (LCNPs) for improved bioavailability. Int. J. Pharm. 2012; 424: 1: 58-66.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Seedher N., Kanojia M. Co-solvent solubilization of some poorly-soluble antidiabetic drugs. Pharm. Dev. Tech. 2009; 14: 2: 185-192.</mixed-citation><mixed-citation xml:lang="en">Seedher N., Kanojia M. Co-solvent solubilization of some poorly-soluble antidiabetic drugs. Pharm. Dev. Tech. 2009; 14: 2: 185-192.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Tiwari G., Tiwari R., Rai K. Studies on development of controlled delivery of combination drug (s) to periodontal pocket. Indian J. Dent. Res. 2010; 21: 1: 72-83.</mixed-citation><mixed-citation xml:lang="en">Tiwari G., Tiwari R., Rai K. Studies on development of controlled delivery of combination drug (s) to periodontal pocket. Indian J. Dent. Res. 2010; 21: 1: 72-83.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Asai K., Morishita M., Katsuta H., et al. The effects of water-soluble cyclodextrins on the histological integrity of the rat nasal mucosa. Int. J. Pharm. 2002; 246: 1: 25-35.</mixed-citation><mixed-citation xml:lang="en">Asai K., Morishita M., Katsuta H., et al. The effects of water-soluble cyclodextrins on the histological integrity of the rat nasal mucosa. Int. J. Pharm. 2002; 246: 1: 25-35.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Del Valle E.M.M. Cyclodextrins and their uses: a review. Process Biochem. 2004; 39: 9: 1033-1046.</mixed-citation><mixed-citation xml:lang="en">Del Valle E.M.M. Cyclodextrins and their uses: a review. Process Biochem. 2004; 39: 9: 1033-1046.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Carrier R.L., Miller L.A., Ahmed I. The utility of cyclodextrins for enhancing oral bioavailability. J. Controlled Release. 2007; 123: 2: 78-99.</mixed-citation><mixed-citation xml:lang="en">Carrier R.L., Miller L.A., Ahmed I. The utility of cyclodextrins for enhancing oral bioavailability. J. Controlled Release. 2007; 123: 2: 78-99.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Géczy J., Bruhwyler J., Scuv?e-Moreau J., et. al. The inclusion of fluoxetine into y-cyclodextrin increases its bioavailability: behavioural, electrophysiological and pharmacokinetic studies. Psychopharm. 2000; 151: 4: 328-334.</mixed-citation><mixed-citation xml:lang="en">Géczy J., Bruhwyler J., Scuv?e-Moreau J., et. al. The inclusion of fluoxetine into y-cyclodextrin increases its bioavailability: behavioural, electrophysiological and pharmacokinetic studies. Psychopharm. 2000; 151: 4: 328-334.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Luengo J., Aranguiz T., Sepulveda J., et. al. Preliminary pharmacokinetic study of different preparations of acyclovir with ß-cyclodextrin. J. Pharm. Sci. 2002; 91: 12: 2593-2598.</mixed-citation><mixed-citation xml:lang="en">Luengo J., Aranguiz T., Sepulveda J., et. al. Preliminary pharmacokinetic study of different preparations of acyclovir with ß-cyclodextrin. J. Pharm. Sci. 2002; 91: 12: 2593-2598.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Berger J., Reist M., Mayer J.M., et al. Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications. Eur. J. Pharm. Biopharm. 2004; 57: 1: 19-34.</mixed-citation><mixed-citation xml:lang="en">Berger J., Reist M., Mayer J.M., et al. Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications. Eur. J. Pharm. Biopharm. 2004; 57: 1: 19-34.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Bhattarai N., Gunn J., Zhang M. Chitosan-based hydrogels for controlled, localized drug delivery. Adv. Drug Deliver. Rev. 2010; 62: 1: 83-99.</mixed-citation><mixed-citation xml:lang="en">Bhattarai N., Gunn J., Zhang M. Chitosan-based hydrogels for controlled, localized drug delivery. Adv. Drug Deliver. Rev. 2010; 62: 1: 83-99.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Desai J., Alexander K., Riga A. Characterization of polymeric dispersions of dimenhydrinate in ethyl cellulose for controlled release. Int. J. Pharm. 2006; 308: 1: 115-123.</mixed-citation><mixed-citation xml:lang="en">Desai J., Alexander K., Riga A. Characterization of polymeric dispersions of dimenhydrinate in ethyl cellulose for controlled release. Int. J. Pharm. 2006; 308: 1: 115-123.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Tanaka N., Imai K., Okimoto K., et. al. Development of novel sustained-release system, disintegration-controlled matrix tablet (DCMT) with solid dispersion granules of nilvadipine (II): in vivo evaluation. J. Controlled Release. 2006; 112: 1: 51-56.</mixed-citation><mixed-citation xml:lang="en">Tanaka N., Imai K., Okimoto K., et. al. Development of novel sustained-release system, disintegration-controlled matrix tablet (DCMT) with solid dispersion granules of nilvadipine (II): in vivo evaluation. J. Controlled Release. 2006; 112: 1: 51-56.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Tran H.T.T., Park J.B., Hong K.-H., et al. Preparation and characterization of pH-independent sustained release tablet containing solid dispersion granules of a poorly water-soluble drug. Int. J. Pharm. 2011; 415: 1: 83-88.</mixed-citation><mixed-citation xml:lang="en">Tran H.T.T., Park J.B., Hong K.-H., et al. Preparation and characterization of pH-independent sustained release tablet containing solid dispersion granules of a poorly water-soluble drug. Int. J. Pharm. 2011; 415: 1: 83-88.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Evrard B., Chiap P., DeTullio P., et al. Oral bioavailability in sheep of albendazole from a suspension and from a solution containing hydroxypropyl-ß-cyclodextrin. J. Controlled Release. 2002; 85: 1: 45-50.</mixed-citation><mixed-citation xml:lang="en">Evrard B., Chiap P., DeTullio P., et al. Oral bioavailability in sheep of albendazole from a suspension and from a solution containing hydroxypropyl-ß-cyclodextrin. J. Controlled Release. 2002; 85: 1: 45-50.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Wong J.W., Yuen K.H. Improved oral bioavailability of artemisinin through inclusion complexation with ß-and y-cyclodextrins. Int. J. Pharm. 2001; 227: 1: 177-185.</mixed-citation><mixed-citation xml:lang="en">Wong J.W., Yuen K.H. Improved oral bioavailability of artemisinin through inclusion complexation with ß-and y-cyclodextrins. Int. J. Pharm. 2001; 227: 1: 177-185.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Ferreira S.M.Z., Domingos G.P., Ferreira D. dos S., et al. Technetium-99m-labeled ceftizoxime loaded long-circulating and pH-sensitive liposomes used to identify osteomyelitis. Bioorg. Med. Chem. Lett. 2012; 22: 14: 4605-4608.</mixed-citation><mixed-citation xml:lang="en">Ferreira S.M.Z., Domingos G.P., Ferreira D. dos S., et al. Technetium-99m-labeled ceftizoxime loaded long-circulating and pH-sensitive liposomes used to identify osteomyelitis. Bioorg. Med. Chem. Lett. 2012; 22: 14: 4605-4608.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Li L., ten Hagen T.L.M., Hossann M., et al. Mild hyperthermia triggered doxorubicin release from optimized stealth thermo sensitive liposomes improves intratumoral drug delivery and efficacy. J. Controlled Release. 2013; 168: 2: 142-150.</mixed-citation><mixed-citation xml:lang="en">Li L., ten Hagen T.L.M., Hossann M., et al. Mild hyperthermia triggered doxorubicin release from optimized stealth thermo sensitive liposomes improves intratumoral drug delivery and efficacy. J. Controlled Release. 2013; 168: 2: 142-150.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Tian H., Tang Z., Zhuang X., et al. Biodegradable synthetic polymers: preparation, functionalization and biomedical application. Prog. Polym. Sci. 2012; 37: 2: 237-280.</mixed-citation><mixed-citation xml:lang="en">Tian H., Tang Z., Zhuang X., et al. Biodegradable synthetic polymers: preparation, functionalization and biomedical application. Prog. Polym. Sci. 2012; 37: 2: 237-280.</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Yao J., Ruan Y., Zhai T., et al. ABC block copolymer as “smart” pH-responsive carrier for intracellular delivery of hydrophobic drugs. Polymer. 2011; 52: 15: 3396-3404.</mixed-citation><mixed-citation xml:lang="en">Yao J., Ruan Y., Zhai T., et al. ABC block copolymer as “smart” pH-responsive carrier for intracellular delivery of hydrophobic drugs. Polymer. 2011; 52: 15: 3396-3404.</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Ramirez E., Burillo S.G., Barrera-Díaz C., et al. Use of pH-sensitive polymer hydrogels in lead removal from aqueous solution. J. Hazard. Mater. 2011; 192: 2: 432-439.</mixed-citation><mixed-citation xml:lang="en">Ramirez E., Burillo S.G., Barrera-Díaz C., et al. Use of pH-sensitive polymer hydrogels in lead removal from aqueous solution. J. Hazard. Mater. 2011; 192: 2: 432-439.</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Yang L., Liu H. Stimuli-responsive magnetic particles and their applications in biomedical field. Powder Technol. 2013; 240: 54-65.</mixed-citation><mixed-citation xml:lang="en">Yang L., Liu H. Stimuli-responsive magnetic particles and their applications in biomedical field. Powder Technol. 2013; 240: 54-65.</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Lee H., Pietrasik J., Sheiko S.S., Matyjaszewski K. Stimuli-responsive molecular brushes. Prog. Polym. Sci. 2010; 35: 1: 24-44.</mixed-citation><mixed-citation xml:lang="en">Lee H., Pietrasik J., Sheiko S.S., Matyjaszewski K. Stimuli-responsive molecular brushes. Prog. Polym. Sci. 2010; 35: 1: 24-44.</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Brun-Graeppi A.K.A.S., Richard C., Bessodes M., et al. Cell microcarriers and microcapsules of stimuli-responsive polymers. J. Controlled Release. 2011; 149: 3: 209-224.</mixed-citation><mixed-citation xml:lang="en">Brun-Graeppi A.K.A.S., Richard C., Bessodes M., et al. Cell microcarriers and microcapsules of stimuli-responsive polymers. J. Controlled Release. 2011; 149: 3: 209-224.</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Hu J., Liu S. Responsive polymers for detection and sensing applications: current status and future developments. Macromolecules. 2010; 43: 20: 8315-8330.</mixed-citation><mixed-citation xml:lang="en">Hu J., Liu S. Responsive polymers for detection and sensing applications: current status and future developments. Macromolecules. 2010; 43: 20: 8315-8330.</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Chiappetta D.A., Sosnik A. Poly (ethylene oxide)-poly (propylene oxide) block copolymer micelles as drug delivery agents: improved hydrosolubility, stability and bioavailability of drugs. Eur. J. Pharm. Biopharm. 2007; 66: 3: 303-317.</mixed-citation><mixed-citation xml:lang="en">Chiappetta D.A., Sosnik A. Poly (ethylene oxide)-poly (propylene oxide) block copolymer micelles as drug delivery agents: improved hydrosolubility, stability and bioavailability of drugs. Eur. J. Pharm. Biopharm. 2007; 66: 3: 303-317.</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Na K., Lee H., Hwang D.J. et al. pH-Sensitivity and pH-dependent structural change in polymeric nanoparticles of poly (vinyl sulfadimethoxine)-deoxycholic acid conjugate. Eur. Polym. J. 2006; 42: 10: 2581-2588.</mixed-citation><mixed-citation xml:lang="en">Na K., Lee H., Hwang D.J. et al. pH-Sensitivity and pH-dependent structural change in polymeric nanoparticles of poly (vinyl sulfadimethoxine)-deoxycholic acid conjugate. Eur. Polym. J. 2006; 42: 10: 2581-2588.</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Park M.-R., Seo B.-B., Song S.-C. Dual ionic interaction system based on polyelectrolyte complex and ionic, injectable, and thermosensitive hydrogel for sustained release of human growth hormone. Biomater. 2013; 34: 4: 1327-1336.</mixed-citation><mixed-citation xml:lang="en">Park M.-R., Seo B.-B., Song S.-C. Dual ionic interaction system based on polyelectrolyte complex and ionic, injectable, and thermosensitive hydrogel for sustained release of human growth hormone. Biomater. 2013; 34: 4: 1327-1336.</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Risbud M. V., Hardikar A., Bhat S. V., Bhonde R.R. pH-sensitive freeze-dried chitosan-polyvinyl pyrrolidone hydrogels as controlled release system for antibiotic delivery. J. Controlled Release. 2000; 68: 1: 23-30.</mixed-citation><mixed-citation xml:lang="en">Risbud M. V., Hardikar A., Bhat S. V., Bhonde R.R. pH-sensitive freeze-dried chitosan-polyvinyl pyrrolidone hydrogels as controlled release system for antibiotic delivery. J. Controlled Release. 2000; 68: 1: 23-30.</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Ghandehari H., Kopecková P., Kopecek J. In vitro degradation of pH-sensitive hydrogels containing aromatic azo bonds. Biomater. 1997; 18: 12: 861-872.</mixed-citation><mixed-citation xml:lang="en">Ghandehari H., Kopecková P., Kopecek J. In vitro degradation of pH-sensitive hydrogels containing aromatic azo bonds. Biomater. 1997; 18: 12: 861-872.</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Shivakumar Hg, Gupta Nv, Satish Cs. Preparation and characterization of gelatin-poly (methacrylic acid) interpenetrating polymeric network hydrogels as a ph-sensitive delivery system for glipizide Indian J. Pharm. Sci. 2007; 69: 1: 64-68.</mixed-citation><mixed-citation xml:lang="en">Shivakumar Hg, Gupta Nv, Satish Cs. Preparation and characterization of gelatin-poly (methacrylic acid) interpenetrating polymeric network hydrogels as a ph-sensitive delivery system for glipizide Indian J. Pharm. Sci. 2007; 69: 1: 64-68.</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Gupta P., Vermani K., Garg S. Hydrogels: from controlled release to pH-responsive drug delivery. Drug Discovery Today. 2002; 7: 10: 569-579.</mixed-citation><mixed-citation xml:lang="en">Gupta P., Vermani K., Garg S. Hydrogels: from controlled release to pH-responsive drug delivery. Drug Discovery Today. 2002; 7: 10: 569-579.</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Wasungu L., Hoekstra D. Cationic lipids, lipoplexes and intracellular delivery of genes. J. Controlled Release. 2006; 116: 2: 255-264.</mixed-citation><mixed-citation xml:lang="en">Wasungu L., Hoekstra D. Cationic lipids, lipoplexes and intracellular delivery of genes. J. Controlled Release. 2006; 116: 2: 255-264.</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Gupta B., Levchenko T., Torchilin V. Intracellular delivery of large molecules and small particles by cell-penetrating proteins and peptides. Adv. Drug Deliver. Rev. 2005; 57: 4: 637-651.</mixed-citation><mixed-citation xml:lang="en">Gupta B., Levchenko T., Torchilin V. Intracellular delivery of large molecules and small particles by cell-penetrating proteins and peptides. Adv. Drug Deliver. Rev. 2005; 57: 4: 637-651.</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Gil E.S. Stimuli-reponsive polymers and their bioconjugates. Prog. Polym. Sci. 2004; 29: 12: 1173-1222.</mixed-citation><mixed-citation xml:lang="en">Gil E.S. Stimuli-reponsive polymers and their bioconjugates. Prog. Polym. Sci. 2004; 29: 12: 1173-1222.</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Park H.-J., Yang F., Cho S.-W. Nonviral delivery of genetic medicine for therapeutic angiogenesis Adv. Drug Deliver. Rev. 2012; 64: 1: 40-52.</mixed-citation><mixed-citation xml:lang="en">Park H.-J., Yang F., Cho S.-W. Nonviral delivery of genetic medicine for therapeutic angiogenesis Adv. Drug Deliver. Rev. 2012; 64: 1: 40-52.</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Green J.J., Langer R., Anderson D.G. A combinatorial polymer library approach yields insight into nonviral gene delivery. Acc. Chem. Res. 2008; 41: 6: 749-759.</mixed-citation><mixed-citation xml:lang="en">Green J.J., Langer R., Anderson D.G. A combinatorial polymer library approach yields insight into nonviral gene delivery. Acc. Chem. Res. 2008; 41: 6: 749-759.</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Sakaguchi N., Kojima C., Harada A., Kono K. Preparation of pH-sensitive poly (glycidol) derivatives with varying hydrophobicities: their ability to sensitize stable liposomes to pH. Bioconjugate Chem. 2008; 19: 5: 1040-1048.</mixed-citation><mixed-citation xml:lang="en">Sakaguchi N., Kojima C., Harada A., Kono K. Preparation of pH-sensitive poly (glycidol) derivatives with varying hydrophobicities: their ability to sensitize stable liposomes to pH. Bioconjugate Chem. 2008; 19: 5: 1040-1048.</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Lee C.H., Kim J.-H., Lee H.J., et al. The generation of iPS cells using non-viral magnetic nanoparticlebased transfection. Biomater. 2011; 32: 28: 6683-6691.</mixed-citation><mixed-citation xml:lang="en">Lee C.H., Kim J.-H., Lee H.J., et al. The generation of iPS cells using non-viral magnetic nanoparticlebased transfection. Biomater. 2011; 32: 28: 6683-6691.</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">Giri T.K., Kumar K., Alexander A., et al. A novel and alternative approach to controlled release drug delivery system based on solid dispersion technique. Bulletin of Faculty of Pharmacy, Cairo University. 2012; 50: 2: 147-159.</mixed-citation><mixed-citation xml:lang="en">Giri T.K., Kumar K., Alexander A., et al. A novel and alternative approach to controlled release drug delivery system based on solid dispersion technique. Bulletin of Faculty of Pharmacy, Cairo University. 2012; 50: 2: 147-159.</mixed-citation></citation-alternatives></ref><ref id="cit85"><label>85</label><citation-alternatives><mixed-citation xml:lang="ru">Kim M.-S., Kim J.-S., Park H.J., et. al. Enhanced bioavailability of sirolimus via preparation of solid dispersion nanoparticles using a supercritical antisolvent process. Int. J. Nanomedicine. 2011; 6: 2997.</mixed-citation><mixed-citation xml:lang="en">Kim M.-S., Kim J.-S., Park H.J., et. al. Enhanced bioavailability of sirolimus via preparation of solid dispersion nanoparticles using a supercritical antisolvent process. Int. J. Nanomedicine. 2011; 6: 2997.</mixed-citation></citation-alternatives></ref><ref id="cit86"><label>86</label><citation-alternatives><mixed-citation xml:lang="ru">Tung N.-T., Park C.-W., Oh T., et al. Formulation of solid dispersion of rebamipide evaluated in a rat model for improved bioavailability and efficacy. J. Pharm. Pharmacol. 2011; 63: 12: 1539-1547.</mixed-citation><mixed-citation xml:lang="en">Tung N.-T., Park C.-W., Oh T., et al. Formulation of solid dispersion of rebamipide evaluated in a rat model for improved bioavailability and efficacy. J. Pharm. Pharmacol. 2011; 63: 12: 1539-1547.</mixed-citation></citation-alternatives></ref><ref id="cit87"><label>87</label><citation-alternatives><mixed-citation xml:lang="ru">Kovacic B., Vrecer F., Planinsek O. Design of a drug delivery system with bimodal pH dependent release of a poorly soluble drug. Die Pharmazie-Int. J. Pharm. Sci. 2011; 66: 6: 465-466.</mixed-citation><mixed-citation xml:lang="en">Kovacic B., Vrecer F., Planinsek O. Design of a drug delivery system with bimodal pH dependent release of a poorly soluble drug. Die Pharmazie-Int. J. Pharm. Sci. 2011; 66: 6: 465-466.</mixed-citation></citation-alternatives></ref><ref id="cit88"><label>88</label><citation-alternatives><mixed-citation xml:lang="ru">Ozeki T., Yuasa H., Kanaya Y. Application of the solid dispersion method to the controlled release of medicine. IX. Difference in the release of flurbiprofen from solid dispersions with poly (ethylene oxide) and hydroxypropylcellulose and the interaction between medicine and polymers. Int. J. Pharm. 1997; 155: 2: 209-217.</mixed-citation><mixed-citation xml:lang="en">Ozeki T., Yuasa H., Kanaya Y. Application of the solid dispersion method to the controlled release of medicine. IX. Difference in the release of flurbiprofen from solid dispersions with poly (ethylene oxide) and hydroxypropylcellulose and the interaction between medicine and polymers. Int. J. Pharm. 1997; 155: 2: 209-217.</mixed-citation></citation-alternatives></ref><ref id="cit89"><label>89</label><citation-alternatives><mixed-citation xml:lang="ru">Swain S.K., Niranjan Patra Ch., Sruti J., Bhanoji Rao M.E. Design and evaluation of sustained release solid dispersions of verapamil hydrochloride. Int. J. Pharm. Sci. Nanotechnol. 2011; 3: 4: 1252-1262.</mixed-citation><mixed-citation xml:lang="en">Swain S.K., Niranjan Patra Ch., Sruti J., Bhanoji Rao M.E. Design and evaluation of sustained release solid dispersions of verapamil hydrochloride. Int. J. Pharm. Sci. Nanotechnol. 2011; 3: 4: 1252-1262.</mixed-citation></citation-alternatives></ref><ref id="cit90"><label>90</label><citation-alternatives><mixed-citation xml:lang="ru">Huang J., Wigent R.J., Schwartz J.B. Nifedipine molecular dispersion in microparticles of ammonio methacrylate copolymer and ethylcellulose binary blends for controlled drug delivery: effect of matrix composition. Drug Dev. Ind. Pharm. 2006; 32: 10: 1185-1197.</mixed-citation><mixed-citation xml:lang="en">Huang J., Wigent R.J., Schwartz J.B. Nifedipine molecular dispersion in microparticles of ammonio methacrylate copolymer and ethylcellulose binary blends for controlled drug delivery: effect of matrix composition. Drug Dev. Ind. Pharm. 2006; 32: 10: 1185-1197.</mixed-citation></citation-alternatives></ref><ref id="cit91"><label>91</label><citation-alternatives><mixed-citation xml:lang="ru">Dangprasirt P., Pongwai S. Development of diclofenac sodium controlled release solid dispersion powders and capsules by freeze drying technique using ethylcellulose and chitosan as carriers. Drug Dev. Ind. Pharm. 1998; 24: 10: 947-953.</mixed-citation><mixed-citation xml:lang="en">Dangprasirt P., Pongwai S. Development of diclofenac sodium controlled release solid dispersion powders and capsules by freeze drying technique using ethylcellulose and chitosan as carriers. Drug Dev. Ind. Pharm. 1998; 24: 10: 947-953.</mixed-citation></citation-alternatives></ref><ref id="cit92"><label>92</label><citation-alternatives><mixed-citation xml:lang="ru">Verreck G., Decorte A., Heymans K., et al. The effect of pressurized carbon dioxide as a temporary plasticizer and foaming agent on the hot stage extrusion process and extrudate properties of solid dispersions of itraconazole with PVP-VA 64. Eur. J. Pharm. Sci. 2005; 26: 3: 349-358.</mixed-citation><mixed-citation xml:lang="en">Verreck G., Decorte A., Heymans K., et al. The effect of pressurized carbon dioxide as a temporary plasticizer and foaming agent on the hot stage extrusion process and extrudate properties of solid dispersions of itraconazole with PVP-VA 64. Eur. J. Pharm. Sci. 2005; 26: 3: 349-358.</mixed-citation></citation-alternatives></ref><ref id="cit93"><label>93</label><citation-alternatives><mixed-citation xml:lang="ru">Ho H.-O., Chen C.-N., Sheu M.-T. Influence of pluronic F-68 on dissolution and bioavailability characteristics of multiple-layer pellets of nifedipine for controlled release delivery J. Controlled Release. 2000; 68: 3: 433-440.</mixed-citation><mixed-citation xml:lang="en">Ho H.-O., Chen C.-N., Sheu M.-T. Influence of pluronic F-68 on dissolution and bioavailability characteristics of multiple-layer pellets of nifedipine for controlled release delivery J. Controlled Release. 2000; 68: 3: 433-440.</mixed-citation></citation-alternatives></ref><ref id="cit94"><label>94</label><citation-alternatives><mixed-citation xml:lang="ru">Qureshi A.I., Cohen R.D. Mesalamine delivery systems: do they really make much difference? Adv. Drug Deliver. Rev. 2005; 57: 2: 281-302.</mixed-citation><mixed-citation xml:lang="en">Qureshi A.I., Cohen R.D. Mesalamine delivery systems: do they really make much difference? Adv. Drug Deliver. Rev. 2005; 57: 2: 281-302.</mixed-citation></citation-alternatives></ref><ref id="cit95"><label>95</label><citation-alternatives><mixed-citation xml:lang="ru">Shah N., Iyer R.M., Mair H.-J., et al. Improved human bioavailability of vemurafenib, a practically insoluble drug, using an amorphous polymer-stabilized solid dispersion prepared by a solvent?controlled coprecipitation process. J. Pharm. Sci. 2013; 102: 3: 967-981.</mixed-citation><mixed-citation xml:lang="en">Shah N., Iyer R.M., Mair H.-J., et al. Improved human bioavailability of vemurafenib, a practically insoluble drug, using an amorphous polymer-stabilized solid dispersion prepared by a solvent?controlled coprecipitation process. J. Pharm. Sci. 2013; 102: 3: 967-981.</mixed-citation></citation-alternatives></ref><ref id="cit96"><label>96</label><citation-alternatives><mixed-citation xml:lang="ru">Augustijns P., Brewster M.E. Supersaturating drug delivery systems: fast is not necessarily good enough. J. Pharm. Sci. 2012; 101: 1: 7-9.</mixed-citation><mixed-citation xml:lang="en">Augustijns P., Brewster M.E. Supersaturating drug delivery systems: fast is not necessarily good enough. J. Pharm. Sci. 2012; 101: 1: 7-9.</mixed-citation></citation-alternatives></ref><ref id="cit97"><label>97</label><citation-alternatives><mixed-citation xml:lang="ru">Shivakumar H.N., Desai B.G., Deshmukh G. Design and optimization of diclofenac sodium controlled release solid dispersions by response surface methodology. Indian J. Pharm. Sci. 2008; 70: 1: 22.</mixed-citation><mixed-citation xml:lang="en">Shivakumar H.N., Desai B.G., Deshmukh G. Design and optimization of diclofenac sodium controlled release solid dispersions by response surface methodology. Indian J. Pharm. Sci. 2008; 70: 1: 22.</mixed-citation></citation-alternatives></ref><ref id="cit98"><label>98</label><citation-alternatives><mixed-citation xml:lang="ru">Tran P.H.-L., Tran T.T.-D., Park J.B., Lee B.-J. Controlled release systems containing solid dispersions: strategies and mechanisms. Pharm. Res. 2011; 28: 10: 2353-2378.</mixed-citation><mixed-citation xml:lang="en">Tran P.H.-L., Tran T.T.-D., Park J.B., Lee B.-J. Controlled release systems containing solid dispersions: strategies and mechanisms. Pharm. Res. 2011; 28: 10: 2353-2378.</mixed-citation></citation-alternatives></ref><ref id="cit99"><label>99</label><citation-alternatives><mixed-citation xml:lang="ru">Tandale P., Joshi D., Gaud R.S. Formulation and Evaluation of Extended Release Solid Dispersions Conatining Simvastatin. Asian J. Biomed. Pharm. Sci. 2011; 1: 3: 13-19.</mixed-citation><mixed-citation xml:lang="en">Tandale P., Joshi D., Gaud R.S. Formulation and Evaluation of Extended Release Solid Dispersions Conatining Simvastatin. Asian J. Biomed. Pharm. Sci. 2011; 1: 3: 13-19.</mixed-citation></citation-alternatives></ref><ref id="cit100"><label>100</label><citation-alternatives><mixed-citation xml:lang="ru">Tran T.T.-D., Tran P.H.-L. Investigation of polyethylene oxide-based prolonged release solid dispersion containing isradipine. J. Drug Deliver. Sci. Technol. 2013; 23: 3: 269-274.</mixed-citation><mixed-citation xml:lang="en">Tran T.T.-D., Tran P.H.-L. Investigation of polyethylene oxide-based prolonged release solid dispersion containing isradipine. J. Drug Deliver. Sci. Technol. 2013; 23: 3: 269-274.</mixed-citation></citation-alternatives></ref><ref id="cit101"><label>101</label><citation-alternatives><mixed-citation xml:lang="ru">Liu X., Wang S., Chai L., et al. A two-step strategy to design high bioavailable controlled-release nimodipine tablets: The push-pull osmotic pump in combination with the micronization/solid dispersion techniques. Int. J. Pharm. 2014; 461: 1: 529-539.</mixed-citation><mixed-citation xml:lang="en">Liu X., Wang S., Chai L., et al. A two-step strategy to design high bioavailable controlled-release nimodipine tablets: The push-pull osmotic pump in combination with the micronization/solid dispersion techniques. Int. J. Pharm. 2014; 461: 1: 529-539.</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>
