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<article article-type="review-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 pub-id-type="doi">10.33380/2305-2066-2024-13-4-1867</article-id><article-id custom-type="elpub" pub-id-type="custom">pharmjournal-1955</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</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PHARMACEUTICAL TECHNOLOGY</subject></subj-group></article-categories><title-group><article-title>Липосомы – метаболически активные транспортные системы лекарственных средств: классификация, составные компоненты, способы изготовления и стабилизации. Часть 1 (обзор)</article-title><trans-title-group xml:lang="en"><trans-title>Liposomes – metabolically active drug transport systems: classification, components, preparation methods, and stabilization. Part 1 (review)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2074-3832</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Осочук</surname><given-names>С. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Osochuk</surname><given-names>S. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>210009, г. Витебск, пр-т Фрунзе, д. 27</p></bio><bio xml:lang="en"><p>27, Frunze avenue, Vitebsk, 210009</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9292-4240</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Коцур</surname><given-names>Ю. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Kotsur</surname><given-names>Yu. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>197022, г. Санкт-Петербург, ул. Профессора Попова, 14, литера А</p></bio><bio xml:lang="en"><p>14A, Prof. Popova str., Saint-Petersburg, 197022</p></bio><email xlink:type="simple">uliya.kocur@spcpu.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1061-0665</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Пожарицкая</surname><given-names>О. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Pozharitskaya</surname><given-names>O. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>183038, г. Мурманск, ул. Владимирская, д. 17</p></bio><bio xml:lang="en"><p>17, Vladimirskaya str., Murmansk, 183038</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8077-2462</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Флисюк</surname><given-names>Е. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Flisyuk</surname><given-names>E. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>197022, г. Санкт-Петербург, ул. Профессора Попова, 14, литера А</p></bio><bio xml:lang="en"><p>14A, Prof. Popova str., Saint-Petersburg, 197022</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0013-4784</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Смехова</surname><given-names>И. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Smekhova</surname><given-names>I. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>197022, г. Санкт-Петербург, ул. Профессора Попова, 14, литера А</p></bio><bio xml:lang="en"><p>14A, Prof. Popova str., Saint-Petersburg, 197022</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0002-5678-672X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Малков</surname><given-names>С. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Malkov</surname><given-names>S. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>197022, г. Санкт-Петербург, ул. Профессора Попова, 14, литера А</p></bio><bio xml:lang="en"><p>14A, Prof. Popova str., Saint-Petersburg, 197022</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0001-1190-5839</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Зарифи</surname><given-names>К. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Zarifi</surname><given-names>K. O.</given-names></name></name-alternatives><bio xml:lang="ru"><p>197022, г. Санкт-Петербург, ул. Профессора Попова, 14, литера А</p></bio><bio xml:lang="en"><p>14A, Prof. Popova str., Saint-Petersburg, 197022</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1343-4663</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Титович</surname><given-names>И. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Titovich</surname><given-names>I. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>197022, г. Санкт-Петербург, ул. Профессора Попова, 14, литера А</p></bio><bio xml:lang="en"><p>14A, Prof. Popova str., Saint-Petersburg, 197022</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7785-4256</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Красова</surname><given-names>Е. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Krasova</surname><given-names>E. K.</given-names></name></name-alternatives><bio xml:lang="ru"><p>197022, г. Санкт-Петербург, ул. Профессора Попова, 14, литера А</p></bio><bio xml:lang="en"><p>14A, Prof. Popova str., Saint-Petersburg, 197022</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4351-0695</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шиков</surname><given-names>А. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Shikov</surname><given-names>A. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>197022, г. Санкт-Петербург, ул. Профессора Попова, 14, литера А</p></bio><bio xml:lang="en"><p>14A, Prof. Popova str., Saint-Petersburg, 197022</p></bio><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Учреждение образования «Витебский государственный ордена Дружбы народов медицинский университет»<country>Беларусь</country></aff><aff xml:lang="en">Vitebsk State Order of Peoples' Friendship Medical University<country>Belarus</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru">Федеральное государственное бюджетное образовательное учреждение высшего образования «Санкт-Петербургский государственный химико-фармацевтический университет» Министерства здравоохранения Российской Федерации (ФГБОУ ВО СПХФУ Минздрава России)<country>Россия</country></aff><aff xml:lang="en">Saint-Petersburg State Chemical and Pharmaceutical University<country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru">Федеральное государственное бюджетное учреждение науки Мурманский морской биологический институт Российской академии наук (ММБИ РАН)<country>Россия</country></aff><aff xml:lang="en">Murmansk Marine Biological Institute of the Russian Academy of Sciences (MMBI RAS)<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>25</day><month>10</month><year>2024</year></pub-date><volume>13</volume><issue>4</issue><fpage>60</fpage><lpage>77</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Осочук С.С., Коцур Ю.М., Пожарицкая О.Н., Флисюк Е.В., Смехова И.Е., Малков С.Д., Зарифи К.О., Титович И.А., Красова Е.К., Шиков А.Н., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Осочук С.С., Коцур Ю.М., Пожарицкая О.Н., Флисюк Е.В., Смехова И.Е., Малков С.Д., Зарифи К.О., Титович И.А., Красова Е.К., Шиков А.Н.</copyright-holder><copyright-holder xml:lang="en">Osochuk S.S., Kotsur Y.M., Pozharitskaya O.N., Flisyuk E.V., Smekhova I.E., Malkov S.D., Zarifi K.O., Titovich I.A., Krasova E.K., Shikov A.N.</copyright-holder><license 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/1955">https://www.pharmjournal.ru/jour/article/view/1955</self-uri><abstract><sec><title>Введение</title><p>Введение. В данном обзоре рассмотрены вопросы современной классификации липосом, методов их изготовления, стабилизации и роли составных компонентов, визуализации, фармакокинетики. В первой части обсуждены первые три вышеупомянутых аспекта.</p></sec><sec><title>Текст</title><p>Текст. Липосомы являются не только перспективными наноконтейнерами для адресной доставки лекарственных средств, но и метаболически активными комплексами с широким спектром активности. Липидные компоненты липосом могут оказать выраженное действие на органы и ткани-мишени. Продукты метаболизма основных компонентов липосом обладают собственной биологической активностью, зависящей от их сочетания и дозировки. Все вышесказанное свидетельствует о перспективности использования липосом не только в качестве носителей ЛС, но и в качестве самостоятельных эффекторов, способных оказать значительное влияние на метаболизм человека при различных заболеваниях. Проведено сравнение преимуществ и ограничений методов получения липосом, рассмотрены особенности изготовления стелс-липосом. Отдельно обсуждены вопросы стабилизации липосом.</p></sec><sec><title>Заключение</title><p>Заключение. Обсужденная в обзоре информация может быть полезна при разработке лекарственных средств в форме липосом.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Introduction</title><p>Introduction. This review article is focused on the modern classification of liposomes, preparation methods, stabilization and the role of structural components, visualization, and pharmacokinetics. Part 1 discusses the first three aspects mentioned above.</p></sec><sec><title>Text</title><p>Text. Depending on the size and number of bilayers, liposomes are classified into simple, long-circulating, cationic, immuno-liposomes, and sterically stabilized. The lipid components of liposomes can have a pronounced effect on target organs and tissues. Metabolites of the main components of liposomes have their biological activity, depending on their combination and dosage. All of the above indicates the promise of using liposomes not only as carriers of drugs but also as independent effectors that can have a significant impact on human metabolism in various diseases. The advantages and limitations of methods for preparing liposomes, and the features for manufacturing stealth liposomes are discussed. A special section of the article is dedicated to liposome stabilization.</p></sec><sec><title>Conclusions</title><p>Conclusions. The information discussed in the review article may be useful in the development of pharmaceutical formulations in liposomes. Liposomes are not only promising nanocontainers for targeted drug delivery, but also metabolically active complexes with a wide spectrum of activity.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>липосомы</kwd><kwd>фосфолипиды</kwd><kwd>метаболизм</kwd><kwd>стабилизация липосом</kwd></kwd-group><kwd-group xml:lang="en"><kwd>liposomes</kwd><kwd>phospholipids</kwd><kwd>metabolism</kwd><kwd>liposomes stabilization</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">Pattni B. S., Chupin V. V., Torchilin V. P. New developments in liposomal drug delivery. Chemical Reviews. 2015;115(19):10938–10966. DOI: 10.1021/acs.chemrev.5b00046.</mixed-citation><mixed-citation xml:lang="en">Pattni B. S., Chupin V. V., Torchilin V. P. New developments in liposomal drug delivery. Chemical Reviews. 2015;115(19):10938–10966. DOI: 10.1021/acs.chemrev.5b00046.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Liu P., Chen G., Zhang J. A review of liposomes as a drug delivery system: Current status of approved products, regulatory environments, and future perspectives. Molecules. 2022;27(4):1372. DOI: 10.3390/molecules27041372.</mixed-citation><mixed-citation xml:lang="en">Liu P., Chen G., Zhang J. A review of liposomes as a drug delivery system: Current status of approved products, regulatory environments, and future perspectives. Molecules. 2022;27(4):1372. DOI: 10.3390/molecules27041372.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Бурдаев Н. И., Николаева Л. Л., Косенко В. В., Шпрах З. С., Бунятян Н. Д. Липосомы как носители лекарственных средств: классификация, методы получения и применение. Ведомости Научного центра экспертизы средств медицинского применения. Регуляторные исследования и экспертиза лекарственных средств. 2023;13(2–1):316–332. DOI: 10.30895/1991-2919-2023-508.</mixed-citation><mixed-citation xml:lang="en">Burdaev N. I., Nikolaeva L. L., Kosenko V. V., Shprah Z. S., Bunyatyan N. D. Liposomes as Drug Carriers: Classification, Preparation Methods, and Medicinal Use. Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products. Regulatory Research and Medicine Evaluation. 2023;13(2–1):316–332. (In Russ.) DOI:10.30895/1991-2919-2023-508.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Jesorka A., Orwar O. Liposomes: technologies and analytical applications. Annual Review of Analytical Chemistry. 2008;1:801–832. DOI: 10.1146/annurev.anchem.1.031207.112747.</mixed-citation><mixed-citation xml:lang="en">Jesorka A., Orwar O. Liposomes: technologies and analytical applications. Annual Review of Analytical Chemistry. 2008;1:801–832. DOI: 10.1146/annurev.anchem.1.031207.112747.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Tokudome Y., Saito Y., Sato F., Kikuchi M., Hinokitani T., Goto K. Preparation and characterization of ceramide-based liposomes with high fusion activity and high membrane fluidity. Colloids and Surfaces B: Biointerfaces. 2009;73(1):92–96. DOI: 10.1016/j.colsurfb.2009.05.002.</mixed-citation><mixed-citation xml:lang="en">Tokudome Y., Saito Y., Sato F., Kikuchi M., Hinokitani T., Goto K. Preparation and characterization of ceramide-based liposomes with high fusion activity and high membrane fluidity. Colloids and Surfaces B: Biointerfaces. 2009;73(1):92–96. DOI: 10.1016/j.colsurfb.2009.05.002.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Spector A. A., Yorek M. A. Membrane lipid composition and cellular function. Journal of Lipid Research. 1985;26(9):1015–1035.</mixed-citation><mixed-citation xml:lang="en">Spector A. A., Yorek M. A. Membrane lipid composition and cellular function. Journal of Lipid Research. 1985;26(9):1015–1035.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Kiss Z. Determination of phospholipase D-mediated hydrolysis of phosphatidylethanolamine. Lipids. 1991;26:321–323. DOI: 10.1007/BF02537144.</mixed-citation><mixed-citation xml:lang="en">Kiss Z. Determination of phospholipase D-mediated hydrolysis of phosphatidylethanolamine. Lipids. 1991;26:321–323. DOI: 10.1007/BF02537144.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Richmond G. S., Smith T. K. Phospholipases A&lt;sub&gt;1&lt;/sub&gt;. International Journal of Molecular Sciences. 2011;12(1):588–612. DOI: 10.3390/ijms12010588.</mixed-citation><mixed-citation xml:lang="en">Richmond G. S., Smith T. K. Phospholipases AA&lt;sub&gt;1&lt;/sub&gt;. International Journal of Molecular Sciences. 2011;12(1):588–612. DOI: 10.3390/ijms12010588.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao Y., Hasse S., Bourgoin S. G. Phosphatidylserine-specific phospholipase A1: A friend or the devil in disguise. Progress in Lipid Research. 2021;83:101112. DOI: 10.1016/j.plipres.2021.101112.</mixed-citation><mixed-citation xml:lang="en">Zhao Y., Hasse S., Bourgoin S. G. Phosphatidylserine-specific phospholipase A1: A friend or the devil in disguise. Progress in Lipid Research. 2021;83:101112. DOI: 10.1016/j.plipres.2021.101112.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Lands W. E. Metabolism of glycerolipids: II. The enzymatic acylation of lysolecithin. Journal of Biological chemistry. 1960;235(8):2233–2237.</mixed-citation><mixed-citation xml:lang="en">Lands W. E. Metabolism of glycerolipids: II. The enzymatic acylation of lysolecithin. Journal of Biological chemistry. 1960;235(8):2233–2237.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Ho C.-L., Lin Y.-L., Li S.-F. Three toxins with phospholipase activity isolated from the yellow-legged hornet (Vespa verutina) venom. Toxicon. 1999;37(7):1015–1024. DOI: 10.1016/s0041-0101(98)00229-3.</mixed-citation><mixed-citation xml:lang="en">Ho C.-L., Lin Y.-L., Li S.-F. Three toxins with phospholipase activity isolated from the yellow-legged hornet (Vespa verutina) venom. Toxicon. 1999;37(7):1015–1024. DOI: 10.1016/s0041-0101(98)00229-3.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Thomson F. J., Clark M. A. Purification of a phosphatidic-acid-hydrolysing phospholipase A 2 from rat brain. Biochemical Journal. 1995;306(1):305–309. DOI: 10.1042/bj3060305.</mixed-citation><mixed-citation xml:lang="en">Thomson F. J., Clark M. A. Purification of a phosphatidic-acid-hydrolysing phospholipase A 2 from rat brain. Biochemical Journal. 1995;306(1):305–309. DOI: 10.1042/bj3060305.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Ren J., Lin J., Yu L., Yan M. Lysophosphatidylcholine: Potential Target for the Treatment of Chronic Pain. International Journal of Molecular Sciences. 2022;23(15):8274. DOI: 10.3390/ijms23158274.</mixed-citation><mixed-citation xml:lang="en">Ren J., Lin J., Yu L., Yan M. Lysophosphatidylcholine: Potential Target for the Treatment of Chronic Pain. International Journal of Molecular Sciences. 2022;23(15):8274. DOI: 10.3390/ijms23158274.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Plemel J. R., Michaels N. J., Weishaupt N., Caprariello A. V., Keough M. B., Rogers J. A., Yukseloglu A., Lim J., Patel V. V., Rawji K. S., Jensen S. K., Teo W., Heyne B., Whitehead S. N., Stys P. K, Yong V. W. Mechanisms of lysophosphatidylcholine-induced demyelination: A primary lipid disrupting myelinopathy. Glia. 2018;66(2):327–347. DOI: 10.1002/glia.23245.</mixed-citation><mixed-citation xml:lang="en">Plemel J. R., Michaels N. J., Weishaupt N., Caprariello A. V., Keough M. B., Rogers J. A., Yukseloglu A., Lim J., Patel V. V., Rawji K. S., Jensen S. K., Teo W., Heyne B., Whitehead S. N., Stys P. K, Yong V. W. Mechanisms of lysophosphatidylcholine-induced demyelination: A primary lipid disrupting myelinopathy. Glia. 2018;66(2):327–347. DOI: 10.1002/glia.23245.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Drzazga A., Sowińska A., Koziołkiewicz M. Lysophosphatidylcholine and lysophosphatidylinosiol--novel promissing signaling molecules and their possible therapeutic activity. Acta poloniae pharmaceutica. 2014;71(6):887–899.</mixed-citation><mixed-citation xml:lang="en">Drzazga A., Sowińska A., Koziołkiewicz M. Lysophosphatidylcholine and lysophosphatidylinosiol--novel promissing signaling molecules and their possible therapeutic activity. Acta poloniae pharmaceutica. 2014;71(6):887–899.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Endo Y., Kanno T., Nakajima T., Ikeda K., Taketomi Y., Yokoyama S., Sasamoto S., Asou H. K., Miyako K., Hasegawa Y., Kawashima Y., Ohara O., Murakami M., Nakayama T. 1-Oleoyl-lysophosphatidylethanolamine stimulates RORγt activity in TH17 cells. Science Immunology. 2023;8(86):eadd4346. DOI: 10.1126/sciimmunol.add4346.</mixed-citation><mixed-citation xml:lang="en">Endo Y., Kanno T., Nakajima T., Ikeda K., Taketomi Y., Yokoyama S., Sasamoto S., Asou H. K., Miyako K., Hasegawa Y., Kawashima Y., Ohara O., Murakami M., Nakayama T. 1-Oleoyl-lysophosphatidylethanolamine stimulates RORγt activity in TH17 cells. Science Immunology. 2023;8(86):eadd4346. DOI: 10.1126/sciimmunol.add4346.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Yamamoto Y., Sakurai T., Chen Z., Inoue N., Chiba H., Hui S.-P. Lysophosphatidylethanolamine Affects Lipid Accumulation and Metabolism in a Human Liver-Derived Cell Line. Nutrients. 2022;14(3):579. DOI: 10.3390/nu14030579.</mixed-citation><mixed-citation xml:lang="en">Yamamoto Y., Sakurai T., Chen Z., Inoue N., Chiba H., Hui S.-P. Lysophosphatidylethanolamine Affects Lipid Accumulation and Metabolism in a Human Liver-Derived Cell Line. Nutrients. 2022;14(3):579. DOI: 10.3390/nu14030579.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Park S.-J., Im D.-S. 2-Arachidonyl-lysophosphatidylethanolamine Induces Anti-Inflammatory Effects on Macrophages and in Carrageenan-Induced Paw Edema. International Journal of Molecular Sciences. 2021;22(9):4865. DOI: 10.3390/ijms22094865.</mixed-citation><mixed-citation xml:lang="en">Park S.-J., Im D.-S. 2-Arachidonyl-lysophosphatidylethanolamine Induces Anti-Inflammatory Effects on Macrophages and in Carrageenan-Induced Paw Edema. International Journal of Molecular Sciences. 2021;22(9):4865. DOI: 10.3390/ijms22094865.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Bill C. A., Vines C. M. Phospholipase C. Calcium signaling. 2020;1131:215–242. DOI: 10.1007/978-3-030-12457-1_9.</mixed-citation><mixed-citation xml:lang="en">Bill C. A., Vines C. M. Phospholipase C. Calcium signaling. 2020;1131:215–242. DOI: 10.1007/978-3-030-12457-1_9.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Takaoka R., Kurosaki H., Nakao H., Ikeda K., Nakano M. Formation of asymmetric vesicles via phospholipase D-mediated transphosphatidylation. Biochimica et Biophysica Acta (BBA)-Biomembranes. 2018;1860(2):245–249. DOI: 10.1016/j.bbamem.2017.10.011.</mixed-citation><mixed-citation xml:lang="en">Takaoka R., Kurosaki H., Nakao H., Ikeda K., Nakano M. Formation of asymmetric vesicles via phospholipase D-mediated transphosphatidylation. Biochimica et Biophysica Acta (BBA)-Biomembranes. 2018;1860(2):245–249. DOI: 10.1016/j.bbamem.2017.10.011.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Hou H.-J., Gong J.-S., Dong Y.-X., Qin J., Li H., Li H., Lu Z.-M., Zhang X.-M., Xu Z.-H., Shi J.-S. Phospholipase D engineering for improving the biocatalytic synthesis of phosphatidylserine. Bioprocess and Biosystems Engineering. 2019;42(7):1185–1194. DOI: 10.1007/s00449-019-02116-7.</mixed-citation><mixed-citation xml:lang="en">Hou H.-J., Gong J.-S., Dong Y.-X., Qin J., Li H., Li H., Lu Z.-M., Zhang X.-M., Xu Z.-H., Shi J.-S. Phospholipase D engineering for improving the biocatalytic synthesis of phosphatidylserine. Bioprocess and Biosystems Engineering. 2019;42(7):1185–1194. DOI: 10.1007/s00449-019-02116-7.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Arora H., Culler M. D., Decker E. A. Production of a High-Phosphatidylserine Lecithin That Synergistically Inhibits Lipid Oxidation with α-Tocopherol in Oil-in-Water Emulsions. Foods. 2022;11(7):1014. DOI: 10.3390/foods11071014.</mixed-citation><mixed-citation xml:lang="en">Arora H., Culler M. D., Decker E. A. Production of a High-Phosphatidylserine Lecithin That Synergistically Inhibits Lipid Oxidation with α-Tocopherol in Oil-in-Water Emulsions. Foods. 2022;11(7):1014. DOI: 10.3390/foods11071014.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Guertin D. A., Sabatini D. M. An expanding role for mTOR in cancer. Trends in Molecular Medicine. 2005;11(8):353–361. DOI: 10.1016/j.molmed.2005.06.007.</mixed-citation><mixed-citation xml:lang="en">Guertin D. A., Sabatini D. M. An expanding role for mTOR in cancer. Trends in Molecular Medicine. 2005;11(8):353–361. DOI: 10.1016/j.molmed.2005.06.007.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Литвинко Н. М. Межфазный катализ липолитических реакций в биоорганической химии: особенности и практическое применение. Известия Национальной академии наук Беларуси. Серия химических наук. 2015;(4):109–121.</mixed-citation><mixed-citation xml:lang="en">Litvinko N. M. Interfacial catalysis of lipolytic reactions in bioorganic chemistry: features and practical application. Proceedings of the National Academy of Sciences of Belarus, Chemical Series. 2015;(4):109–121. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Aguilar A., Saba J. D. Truth and consequences of sphingosine-1-phosphate lyase. Advances in Biological Regulation. 2012;52(1):17–30. DOI: 10.1016/j.advenzreg.2011.09.015.</mixed-citation><mixed-citation xml:lang="en">Aguilar A., Saba J. D. Truth and consequences of sphingosine-1-phosphate lyase. Advances in Biological Regulation. 2012;52(1):17–30. DOI: 10.1016/j.advenzreg.2011.09.015.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Iqbal J., Walsh M. T., Hammad S. M., Hussain M. M. Sphingolipids and Lipoproteins in Health and Metabolic Disorders. Trends in Endocrinology &amp; Metabolism. 2017;28(7):506–518. DOI: 10.1016/j.tem.2017.03.005.</mixed-citation><mixed-citation xml:lang="en">Iqbal J., Walsh M. T., Hammad S. M., Hussain M. M. Sphingolipids and Lipoproteins in Health and Metabolic Disorders. Trends in Endocrinology &amp; Metabolism. 2017;28(7):506–518. DOI: 10.1016/j.tem.2017.03.005.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Gulbins A., Grassmé H., Hoehn R., Wilker B., Soddemann M., Kohnen M., Edwards M. J., Kornhuber J., Gulbins E. Regulation of Neuronal Stem Cell Proliferation in the Hippocampus by Endothelial Ceramide. Cellular Physiology and Biochemistry. 2016;39(2):790–801. DOI: 10.1159/000447789.</mixed-citation><mixed-citation xml:lang="en">Gulbins A., Grassmé H., Hoehn R., Wilker B., Soddemann M., Kohnen M., Edwards M. J., Kornhuber J., Gulbins E. Regulation of Neuronal Stem Cell Proliferation in the Hippocampus by Endothelial Ceramide. Cellular Physiology and Biochemistry. 2016;39(2):790–801. DOI: 10.1159/000447789.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Cruciani-Guglielmacci C., López M., Campana M., Le Stunff H. Brain Ceramide Metabolism in the Control of Energy Balance. Frontiers in Physiology. 2017;8:787. DOI: 10.3389/fphys.2017.00787.</mixed-citation><mixed-citation xml:lang="en">Cruciani-Guglielmacci C., López M., Campana M., Le Stunff H. Brain Ceramide Metabolism in the Control of Energy Balance. Frontiers in Physiology. 2017;8:787. DOI: 10.3389/fphys.2017.00787.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Jana A., Hogan E. L., Pahan K. Ceramide and neurodegeneration: susceptibility of neurons and oligodendrocytes to cell damage and death. Journal of the Neurological Sciences. 2009;278(1–2):5–15. DOI: 10.1016/j.jns.2008.12.010.</mixed-citation><mixed-citation xml:lang="en">Jana A., Hogan E. L., Pahan K. Ceramide and neurodegeneration: susceptibility of neurons and oligodendrocytes to cell damage and death. Journal of the Neurological Sciences. 2009;278(1–2):5–15. DOI: 10.1016/j.jns.2008.12.010.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Jiang M., Chavarria T. E., Yuan B., Lodish H. F., Huang N.-J. Phosphocholine accumulation and PHOSPHO1 depletion promote adipose tissue thermogenesis. Proceedings of the National Academy of Sciences. 2020;117(26):15055–15065. DOI: 10.1073/pnas.1916550117.</mixed-citation><mixed-citation xml:lang="en">Jiang M., Chavarria T. E., Yuan B., Lodish H. F., Huang N.-J. Phosphocholine accumulation and PHOSPHO1 depletion promote adipose tissue thermogenesis. Proceedings of the National Academy of Sciences. 2020;117(26):15055–15065. DOI: 10.1073/pnas.1916550117.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Grabitzki J., Lochnit G. Immunomodulation by phosphocholine–biosynthesis, structures and immunological implications of parasitic PC-epitopes. Molecular Immunology. 2009;47(2–3):149–163. DOI: 10.1016/j.molimm.2009.09.035.</mixed-citation><mixed-citation xml:lang="en">Grabitzki J., Lochnit G. Immunomodulation by phosphocholine–biosynthesis, structures and immunological implications of parasitic PC-epitopes. Molecular Immunology. 2009;47(2–3):149–163. DOI: 10.1016/j.molimm.2009.09.035.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Clark S. E., Weiser J. N. Microbial modulation of host immunity with the small molecule phosphorylcholine. Infection and Immunity. 2013;81(2):392–401. DOI: 10.1128/IAI.01168-12.</mixed-citation><mixed-citation xml:lang="en">Clark S. E., Weiser J. N. Microbial modulation of host immunity with the small molecule phosphorylcholine. Infection and Immunity. 2013;81(2):392–401. DOI: 10.1128/IAI.01168-12.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Cartier A., Hla T. Sphingosine 1-phosphate: Lipid signaling in pathology and therapy. Science. 2019;366(6463):eaar5551. DOI: 10.1126/science.aar5551.</mixed-citation><mixed-citation xml:lang="en">Cartier A., Hla T. Sphingosine 1-phosphate: Lipid signaling in pathology and therapy. Science. 2019;366(6463):eaar5551. DOI: 10.1126/science.aar5551.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Hodun K., Chabowski A., Baranowski M. Sphingosine-1-phosphate in acute exercise and training. Scandinavian Journal of Medicine &amp; Science in Sports. 2021;31(5):945–955. DOI: 10.1111/sms.13907.</mixed-citation><mixed-citation xml:lang="en">Hodun K., Chabowski A., Baranowski M. Sphingosine-1-phosphate in acute exercise and training. Scandinavian Journal of Medicine &amp; Science in Sports. 2021;31(5):945–955. DOI: 10.1111/sms.13907.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Blanc M., Hsieh W. Y., Robertson K. A., Kropp K. A., Forster T., Shui G., Lacaze P., Watterson S., Griffiths S. J., Spann N. J., Meljon A., Talbot S., Krishnan K., Covey D. F., Wenk M. R., Craigon M., Ruzsics Z., Haas J., Angulo A., Griffiths W. J., Glass C. K., Wang Y., Ghazal P. The transcription factor STAT-1 couples macrophage synthesis of 25-hydroxycholesterol to the interferon antiviral response. Immunity. 2013;38(1):106–118. DOI: 10.1016/j.immuni.2012.11.004.</mixed-citation><mixed-citation xml:lang="en">Blanc M., Hsieh W. Y., Robertson K. A., Kropp K. A., Forster T., Shui G., Lacaze P., Watterson S., Griffiths S. J., Spann N. J., Meljon A., Talbot S., Krishnan K., Covey D. F., Wenk M. R., Craigon M., Ruzsics Z., Haas J., Angulo A., Griffiths W. J., Glass C. K., Wang Y., Ghazal P. The transcription factor STAT-1 couples macrophage synthesis of 25-hydroxycholesterol to the interferon antiviral response. Immunity. 2013;38(1):106–118. DOI: 10.1016/j.immuni.2012.11.004.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Zang R., Case J. B., Yutuc E., Ma X., Shen S., Gomez Castro M. F., Liua Z., Zeng Q., Zhao H., Son J., Rothlauf P. W., Kreutzberger A. J. B., Hou G., Zhang H., Bosem S., Wang X., Vahey M. D., Mani K., Griffiths W. J., Kirchhausen T., Fremont D. H., Guo H., Diwane A., Wang Y., Diamond M. S., Whelan S. P. J., Ding S. Cholesterol 25-hydroxylase suppresses SARS-CoV-2 replication by blocking membrane fusion. Proceedings of the National Academy of Sciences. 2020;117(50):32105–32113. DOI: 10.1073/pnas.2012197117.</mixed-citation><mixed-citation xml:lang="en">Zang R., Case J. B., Yutuc E., Ma X., Shen S., Gomez Castro  M. F., Liua Z., Zeng Q., Zhao H., Son J., Rothlauf P. W., Kreutzberger A. J. B., Hou G., Zhang H., Bosem S., Wang X., Vahey M. D., Mani K., Griffiths W. J., Kirchhausen T., Fremont D. H., Guo H., Diwane A., Wang Y., Diamond M. S., Whelan S. P. J., Ding S. Cholesterol 25-hydroxylase suppresses SARS-CoV-2 replication by blocking membrane fusion. Proceedings of the National Academy of Sciences. 2020;117(50):32105–32113. DOI: 10.1073/pnas.2012197117.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Griffiths W. J., Wang Y. Cholesterol metabolism: from lipidomics to immunology. Journal of Lipid Research. 2022;63(2):100165. DOI: 10.1016/j.jlr.2021.100165.</mixed-citation><mixed-citation xml:lang="en">Griffiths W. J., Wang Y. Cholesterol metabolism: from lipidomics to immunology. Journal of Lipid Research. 2022;63(2):100165. DOI: 10.1016/j.jlr.2021.100165.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Chambers K. F., Day P. E., Aboufarrag H. T., Kroon P. A. Polyphenol effects on cholesterol metabolism via bile acid biosynthesis, CYP7A1: A Review. Nutrients. 2019;11(11):2588. DOI: 10.3390/nu11112588.</mixed-citation><mixed-citation xml:lang="en">Chambers K. F., Day P. E., Aboufarrag H. T., Kroon P. A. Polyphenol effects on cholesterol metabolism via bile acid biosynthesis, CYP7A1: A Review. Nutrients. 2019;11(11):2588. DOI: 10.3390/nu11112588.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang J., Zhu Y., Wang X., Wang J. 25-hydroxycholesterol: an integrator of antiviral ability and signaling. Frontiers in Immunology. 2023;14:1268104. DOI: 10.3389/fimmu.2023.1268104.</mixed-citation><mixed-citation xml:lang="en">Zhang J., Zhu Y., Wang X., Wang J. 25-hydroxycholesterol: an integrator of antiviral ability and signaling. Frontiers in Immunology. 2023;14:1268104. DOI: 10.3389/fimmu.2023.1268104.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Kakiyama G., Minowa K., Rodriguez-Agudo D., Martin R., Takei H., Mitamura K., Ikegawa S., Suzuki M., Nittono H., Fuchs M., Heuman D. M., Zhou H., Pandak W. M. Coffee modulates insulin-hepatocyte nuclear factor-4α-Cyp7b1 pathway and reduces oxysterol-driven liver toxicity in a nonalcoholic fatty liver disease mouse model. American Journal of Physiology-Gastrointestinal and Liver Physiology. 2022;323(5):G488–G500. DOI: 10.1152/ajpgi.00179.2022.</mixed-citation><mixed-citation xml:lang="en">Kakiyama G., Minowa K., Rodriguez-Agudo D., Martin R., Takei H., Mitamura K., Ikegawa S., Suzuki M., Nittono H., Fuchs M., Heuman D. M., Zhou H., Pandak W. M. Coffee modulates insulin-hepatocyte nuclear factor-4α-Cyp7b1 pathway and reduces oxysterol-driven liver toxicity in a nonalcoholic fatty liver disease mouse model. American Journal of Physiology-Gastrointestinal and Liver Physiology. 2022;323(5):G488–G500. DOI: 10.1152/ajpgi.00179.2022.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Chiang J. Y. L., Ferrell J. M. Up to date on cholesterol 7 alpha-hydroxylase (CYP7A1) in bile acid synthesis. Liver Research. 2020;4(2):47–63. DOI: 10.1016/j.livres.2020.05.001.</mixed-citation><mixed-citation xml:lang="en">Chiang J. Y. L., Ferrell J. M. Up to date on cholesterol 7 alpha-hydroxylase (CYP7A1) in bile acid synthesis. Liver Research. 2020;4(2):47–63. DOI: 10.1016/j.livres.2020.05.001.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Noguchi N., Saito Y., Urano Y. Diverse functions of 24(S)-hydroxycholesterol in the brain. Biochemical and Biophysical Research Communications. 2014;446(3):692–696. DOI: 10.1016/j.bbrc.2014.02.010.</mixed-citation><mixed-citation xml:lang="en">Noguchi N., Saito Y., Urano Y. Diverse functions of 24(S)-hydroxycholesterol in the brain. Biochemical and Biophysical Research Communications. 2014;446(3):692–696. DOI: 10.1016/j.bbrc.2014.02.010.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Bikle D., Christakos S. New aspects of vitamin D metabolism and action – addressing the skin as source and target. Nature Reviews Endocrinology. 2020;16(4):234-252. DOI: 10.1038/s41574-019-0312-5.</mixed-citation><mixed-citation xml:lang="en">Bikle D., Christakos S. New aspects of vitamin D metabolism and action – addressing the skin as source and target. Nature Reviews Endocrinology. 2020;16(4):234-252. DOI: 10.1038/s41574-019-0312-5.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Титов В. Н. Атеросклероз как патология полиеновых жирных кислот. Биологические основы теории атерогенеза. Москва: Клиника XXI века; 2002. 495 с.</mixed-citation><mixed-citation xml:lang="en">Titov V. N. Atherosclerosis as a pathology of polyene fatty acids. Biological basis of the theory of atherogenesis. Moscow: Klinika XXI veka; 2002. 495 p. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Wang B., Wu L., Chen J., Dong L., Chen C., Wen Z., Hu J., Fleming I., Wang D. W. Metabolism pathways of arachidonic acids: mechanisms and potential therapeutic targets. Signal Transduction and Targeted Therapy. 2021;6(1):94. DOI: 10.1038/s41392-020-00443-w.</mixed-citation><mixed-citation xml:lang="en">Wang B., Wu L., Chen J., Dong L., Chen C., Wen Z., Hu J., Fleming I., Wang D. W. Metabolism pathways of arachidonic acids: mechanisms and potential therapeutic targets. Signal Transduction and Targeted Therapy. 2021;6(1):94. DOI: 10.1038/s41392-020-00443-w.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Biernacki M., Skrzydlewska E. Metabolism of endocannabinoids. Postępy Higieny i Medycyny Doświadczalnej. 2016;70(0):830–843. DOI: 10.5604/17322693.1213898.</mixed-citation><mixed-citation xml:lang="en">Biernacki M., Skrzydlewska E. Metabolism of endocannabinoids. Postępy Higieny i Medycyny Doświadczalnej. 2016;70(0):830–843. DOI: 10.5604/17322693.1213898.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Serhan C. N., Levy B. D. Resolvins in inflammation: emergence of the pro-resolving superfamily of mediators. Journal of Clinical Investigation. 2018;128(7):2657–2669. DOI: 10.1172/JCI97943.</mixed-citation><mixed-citation xml:lang="en">Serhan C. N., Levy B. D. Resolvins in inflammation: emergence of the pro-resolving superfamily of mediators. Journal of Clinical Investigation. 2018;128(7):2657–2669. DOI: 10.1172/JCI97943.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Hu J., Lin S., Zheng B., Cheung P. C. K. Short-chain fatty acids in control of energy metabolism. Critical Reviews in Food Science and Nutrition. 2018;58(8):1243–1249. DOI: 10.1080/10408398.2016.1245650.</mixed-citation><mixed-citation xml:lang="en">Hu J., Lin S., Zheng B., Cheung P. C. K. Short-chain fatty acids in control of energy metabolism. Critical Reviews in Food Science and Nutrition. 2018;58(8):1243–1249. DOI: 10.1080/10408398.2016.1245650.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">De Carvalho C. C. R., Caramujo M. J. The Various roles of fatty acids. Molecules. 2018;23(10):2583. DOI: 10.3390/molecules23102583.</mixed-citation><mixed-citation xml:lang="en">De Carvalho C. C. R., Caramujo M. J. The Various roles of fatty acids. Molecules. 2018;23(10):2583. DOI: 10.3390/molecules23102583.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Bangham A. D., Standish M. M., Weissmann G. The action of steroids and streptolysin S on the permeability of phospholipid structures to cations. Journal of Molecular Biology. 1965;13(1):253–259. DOI: 10.1016/S0022-2836(65)80094-8.</mixed-citation><mixed-citation xml:lang="en">Bangham A. D., Standish M. M., Weissmann G. The action of steroids and streptolysin S on the permeability of phospholipid structures to cations. Journal of Molecular Biology. 1965;13(1):253–259. DOI: 10.1016/S0022-2836(65)80094-8.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Brunner J., Skrabal P., Hauser H. Single bilayer vesicles prepared without sonication physico-chemical properties. Biochimica et Biophysica Acta (BBA) – Biomembranes. 1976;455(2):322–331. DOI: 10.1016/0005-2736(76)90308-4.</mixed-citation><mixed-citation xml:lang="en">Brunner J., Skrabal P., Hauser H. Single bilayer vesicles prepared without sonication physico-chemical properties. Biochimica et Biophysica Acta (BBA) – Biomembranes. 1976;455(2):322–331. DOI: 10.1016/0005-2736(76)90308-4.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Batzri S., Korn E. D. Single bilayer liposomes prepared without sonication. Biochimica et Biophysica Acta (BBA) – Biomembranes. 1973;298(4):1015–1019. DOI: 10.1016/0005-2736(73)90408-2.</mixed-citation><mixed-citation xml:lang="en">Batzri S., Korn E. D. Single bilayer liposomes prepared without sonication. Biochimica et Biophysica Acta (BBA) – Biomembranes. 1973;298(4):1015–1019. DOI: 10.1016/0005-2736(73)90408-2.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Szoka F., Papahadjopoulos D. Procedure for preparation of liposomes with large internal aqueous space and high capture by reverse-phase evaporation. Proceedings of the National Academy of Sciences. 1978;75(9):4194–4198. DOI: 10.1073/pnas.75.9.4194.</mixed-citation><mixed-citation xml:lang="en">Szoka F., Papahadjopoulos D. Procedure for preparation of liposomes with large internal aqueous space and high capture by reverse-phase evaporation. Proceedings of the National Academy of Sciences. 1978;75(9):4194–4198. DOI: 10.1073/pnas.75.9.4194.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">New R. R. Liposomes. Oxford: IRL at Oxford University Press; 1990. 301 p.</mixed-citation><mixed-citation xml:lang="en">New R. R. Liposomes. Oxford: IRL at Oxford University Press; 1990. 301 p.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Kim S., Martin G. M. Preparation of cell-size unilamellar liposomes with high captured volume and defined size distribution. Biochimica et Biophysica Acta (BBA) – Biomembranes. 1981;646(1):1–9. DOI: 10.1016/0005-2736(81)90264-9.</mixed-citation><mixed-citation xml:lang="en">Kim S., Martin G. M. Preparation of cell-size unilamellar liposomes with high captured volume and defined size distribution. Biochimica et Biophysica Acta (BBA) – Biomembranes. 1981;646(1):1–9. DOI: 10.1016/0005-2736(81)90264-9.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Karn P.-R., Cho W., Park H. J., Park J. S., Hwang S. J. Characterization and stability studies of a novel liposomal cyclosporin A prepared using the supercritical fluid method: comparison with the modified conventional Bangham method. International Journal of Nanomedicine. 2013:365–377. DOI: 10.2147/IJN.S39025.</mixed-citation><mixed-citation xml:lang="en">Karn P.-R., Cho W., Park H. J., Park J. S., Hwang S. J. Characterization and stability studies of a novel liposomal cyclosporin A prepared using the supercritical fluid method: comparison with the modified conventional Bangham method. International Journal of Nanomedicine. 2013:365–377. DOI: 10.2147/IJN.S39025.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Nicolosi D., Scalia M., Nicolosi V. M., Pignatello R. Encapsulation in fusogenic liposomes broadens the spectrum of action of vancomycin against Gram-negative bacteria. International Journal of Antimicrobial Agents. 2010;35(6):553–558. DOI: 10.1016/j.ijantimicag.2010.01.015.</mixed-citation><mixed-citation xml:lang="en">Nicolosi D., Scalia M., Nicolosi V. M., Pignatello R. Encapsulation in fusogenic liposomes broadens the spectrum of action of vancomycin against Gram-negative bacteria. International Journal of Antimicrobial Agents. 2010;35(6):553–558. DOI: 10.1016/j.ijantimicag.2010.01.015.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Lehmann J., Agel M. R., Engelhardt K. H., Pinnapireddy S. R., Agel S., Duse L., Preis E., Wojcik M., Bakowsky U. Improvement of pulmonary photodynamic therapy: Nebulisation of curcumin-loaded tetraether liposomes. Pharmaceutics. 2021;13(8):1243. DOI: 10.3390/pharmaceutics13081243.</mixed-citation><mixed-citation xml:lang="en">Lehmann J., Agel M. R., Engelhardt K. H., Pinnapireddy S. R., Agel S., Duse L., Preis E., Wojcik M., Bakowsky U. Improvement of pulmonary photodynamic therapy: Nebulisation of curcumin-loaded tetraether liposomes. Pharmaceutics. 2021;13(8):1243. DOI: 10.3390/pharmaceutics13081243.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Phapal S. M., Sunthar P. Influence of micro-mixing on the size of liposomes self-assembled from miscible liquid phases. Chemistry and Physics of Lipids. 2013;172:20–30. DOI: 10.1016/j.chemphyslip.2013.04.006.</mixed-citation><mixed-citation xml:lang="en">Phapal S. M., Sunthar P. Influence of micro-mixing on the size of liposomes self-assembled from miscible liquid phases. Chemistry and Physics of Lipids. 2013;172:20–30. DOI: 10.1016/j.chemphyslip.2013.04.006.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Mozafari M. R., Reed C. J., Rostron C. Cytotoxicity evaluation of anionic nanoliposomes and nanolipoplexes prepared by the heating method without employing volatile solvents and detergents. Pharmazie. 2007;62(3):205–209.</mixed-citation><mixed-citation xml:lang="en">Mozafari M. R., Reed C. J., Rostron C. Cytotoxicity evaluation of anionic nanoliposomes and nanolipoplexes prepared by the heating method without employing volatile solvents and detergents. Pharmazie. 2007;62(3):205–209.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Saliba A.-E., Vonkova I., Deghou S., Ceschia S., Tischer C., Kugler K. G., Bork P., Ellenberg J., Gavin A.-C. A protocol for the systematic and quantitative measurement of protein-lipid interactions using the liposome-microarray-based assay. Nature Protocols. 2016; 11(6):1021–1038. DOI: 10.1038/nprot.2016.059.</mixed-citation><mixed-citation xml:lang="en">Saliba A.-E., Vonkova I., Deghou S., Ceschia S., Tischer C., Kugler K. G., Bork P., Ellenberg J., Gavin A.-C. A protocol for the systematic and quantitative measurement of protein-lipid interactions using the liposome-microarray-based assay. Nature Protocols. 2016; 11(6):1021–1038. DOI: 10.1038/nprot.2016.059.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Devrim B., Kara A., Vural İ., Bozkır A. Lysozyme-loaded lipid-polymer hybrid nanoparticles: preparation, characterization and colloidal stability evaluation. Drug Development and Industrial Pharmacy. 2016;42(11):1865–1876. DOI: 10.1080/03639045.2016.1180392.</mixed-citation><mixed-citation xml:lang="en">Devrim B., Kara A., Vural İ., Bozkır A. Lysozyme-loaded lipid-polymer hybrid nanoparticles: preparation, characterization and colloidal stability evaluation. Drug Development and Industrial Pharmacy. 2016;42(11):1865–1876. DOI: 10.1080/03639045.2016.1180392.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Anabousi S., Laue M., Lehr C.-M., Bakowsky U., Ehrhardt C. Assessing transferrin modification of liposomes by atomic force microscopy and transmission electron microscopy. European Journal of Pharmaceutics and Biopharmaceutics. 2005;60(2):295–303. DOI: 10.1016/j.ejpb.2004.12.009.</mixed-citation><mixed-citation xml:lang="en">Anabousi S., Laue M., Lehr C.-M., Bakowsky U., Ehrhardt C. Assessing transferrin modification of liposomes by atomic force microscopy and transmission electron microscopy. European Journal of Pharmaceutics and Biopharmaceutics. 2005;60(2):295–303. DOI: 10.1016/j.ejpb.2004.12.009.</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Sivadasan D., Sultan M. H., Madkhali O. A., Alsabei S. H., Alessa A. A. Stealth liposomes (PEGylated) containing an anticancer drug camptothecin: In vitro characterization and in vivo pharmacokinetic and tissue distribution study. Molecules. 2022;27(3):1086. DOI: 10.3390/molecules27031086.</mixed-citation><mixed-citation xml:lang="en">Sivadasan D., Sultan M. H., Madkhali O. A., Alsabei S. H., Alessa A. A. Stealth liposomes (PEGylated) containing an anticancer drug camptothecin: In vitro characterization and in vivo pharmacokinetic and tissue distribution study. Molecules. 2022;27(3):1086. DOI: 10.3390/molecules27031086.</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Shetti P., Jalalpure S. S., Patil A. S., Kaur K. Apigenin-loaded stealth liposomes: Development and pharmacokinetic studies for enhanced plasma retention of drug in cancer therapy. Topics in Catalysis. 2024;67(1):46–58. DOI: 10.1007/s11244-023-01818-3.</mixed-citation><mixed-citation xml:lang="en">Shetti P., Jalalpure S. S., Patil A. S., Kaur K. Apigenin-loaded stealth liposomes: Development and pharmacokinetic studies for enhanced plasma retention of drug in cancer therapy. Topics in Catalysis. 2024;67(1):46–58. DOI: 10.1007/s11244-023-01818-3.</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Gheibi Hayat S. M., Jaafari M. R., Hatamipour M., Penson P. E., Sahebkar A. Liposome circulation time is prolonged by CD47 coating. Protein &amp; Peptide Letters. 2020;27(10):1029–1037. DOI: 10.2174/0929866527666200413100120.</mixed-citation><mixed-citation xml:lang="en">Gheibi Hayat S. M., Jaafari M. R., Hatamipour M., Penson P. E., Sahebkar A. Liposome circulation time is prolonged by CD47 coating. Protein &amp; Peptide Letters. 2020;27(10):1029–1037. DOI: 10.2174/0929866527666200413100120.</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Wang Z., Zhao Y., Jiang Y., Lv W., Wu L., Wang B., Lv L., Xu Q., Xin H. Enhanced anti-ischemic stroke of ZL006 by T7-conjugated PEGylated liposomes drug delivery system. Scientific Reports. 2015;5(1):12651. DOI: 10.1038/srep12651.</mixed-citation><mixed-citation xml:lang="en">Wang Z., Zhao Y., Jiang Y., Lv W., Wu L., Wang B., Lv L., Xu Q., Xin H. Enhanced anti-ischemic stroke of ZL006 by T7-conjugated PEGylated liposomes drug delivery system. Scientific Reports. 2015;5(1):12651. DOI: 10.1038/srep12651.</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Sylvester B., Porfire A., Muntean D.-M., Vlase L., Lupuţ L., Licarete E., Sesarman A., Costel Alupei M., Banciu M., Achim M., Tomuţă I. Optimization of prednisolone-loaded long-circulating liposomes via application of Quality by Design (QbD) approach. Journal of Liposome Research. 2018;28(1):49–61. DOI: 10.1080/08982104.2016.1254242.</mixed-citation><mixed-citation xml:lang="en">Sylvester B., Porfire A., Muntean D.-M., Vlase L., Lupuţ L., Licarete E., Sesarman A., Costel Alupei M., Banciu M., Achim M., Tomuţă I. Optimization of prednisolone-loaded long-circulating liposomes via application of Quality by Design (QbD) approach. Journal of Liposome Research. 2018;28(1):49–61. DOI: 10.1080/08982104.2016.1254242.</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Maherani B., Arab-Tehrany E., Mozafari M. R., Gaiani C., Linder M. Liposomes: A Review of Manufacturing Techniques and Targeting Strategies. Current Nanoscience. 2011;7(3):436–52. DOI: 10.2174/157341311795542453.</mixed-citation><mixed-citation xml:lang="en">Maherani B., Arab-Tehrany E., Mozafari M. R., Gaiani C., Linder M. Liposomes: A Review of Manufacturing Techniques and Targeting Strategies. Current Nanoscience. 2011;7(3):436–52. DOI: 10.2174/157341311795542453.</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Crowe L. M., Crowe J. H., Rudolph A., Womersley C., Appel L. Preservation of freeze-dried liposomes by trehalose. Archives of Biochemistry and Biophysics. 1985;242(1):240–247. DOI: 10.1016/0003-9861(85)90498-9.</mixed-citation><mixed-citation xml:lang="en">Crowe L. M., Crowe J. H., Rudolph A., Womersley C., Appel L. Preservation of freeze-dried liposomes by trehalose. Archives of Biochemistry and Biophysics. 1985;242(1):240–247. DOI: 10.1016/0003-9861(85)90498-9.</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Stark B., Pabst G., Prassl R. Long-term stability of sterically stabilized liposomes by freezing and freeze-drying: Effects of cryoprotectants on structure. European Journal of Pharmaceutical Sciences. 2010;41(3–4):546–555. DOI: 10.1016/j.ejps.2010.08.010.</mixed-citation><mixed-citation xml:lang="en">Stark B., Pabst G., Prassl R. Long-term stability of sterically stabilized liposomes by freezing and freeze-drying: Effects of cryoprotectants on structure. European Journal of Pharmaceutical Sciences. 2010;41(3–4):546–555. DOI: 10.1016/j.ejps.2010.08.010.</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Stadnichenko O. V., Krasnopolsky Y. M., Yarnykh T. G. The study of liophilization parameters in the liposomal irinotecan development. News of Pharmacy. 2017;4(92):45–49.</mixed-citation><mixed-citation xml:lang="en">Stadnichenko O. V., Krasnopolsky Y. M., Yarnykh T. G. The study of liophilization parameters in the liposomal irinotecan development. News of Pharmacy. 2017;4(92):45–49.</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Franzé S., Selmin F., Samaritani E., Minghetti P., Cilurzo F. Lyophilization of liposomal formulations: still necessary, still challenging. Pharmaceutics. 2018;10(3):139. DOI: 10.3390/pharmaceutics10030139.</mixed-citation><mixed-citation xml:lang="en">Franzé S., Selmin F., Samaritani E., Minghetti P., Cilurzo F. Lyophilization of liposomal formulations: still necessary, still challenging. Pharmaceutics. 2018;10(3):139. DOI: 10.3390/pharmaceutics10030139.</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Filipe V., Hawe A., Jiskoot W. Critical evaluation of nanoparticle tracking analysis (NTA) by nanosight for the measurement of nanoparticles and protein aggregates. Pharmaceutical Research. 2010;27:796–810. DOI: 10.1007/s11095-010-0073-2.</mixed-citation><mixed-citation xml:lang="en">Filipe V., Hawe A., Jiskoot W. Critical evaluation of nanoparticle tracking analysis (NTA) by nanosight for the measurement of nanoparticles and protein aggregates. Pharmaceutical Research. 2010;27:796–810. DOI: 10.1007/s11095-010-0073-2.</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Pedreira de Almeida A. C., Matos Alves Pinto L., Piovesan Alves G., Nunes de Morais Ribeiro L., Andrade Santana M. H., Saia Cereda C. M., Fernandes Fraceto L., de Paula E. Liposomal-based lidocaine formulation for the improvement of infiltrative buccal anaesthesia. Journal of Liposome Research. 2019;29(1),66–72. DOI: 10.1080/08982104.2018.1483947.</mixed-citation><mixed-citation xml:lang="en">Pedreira de Almeida A. C., Matos Alves Pinto L., Piovesan Alves G., Nunes de Morais Ribeiro L., Andrade Santana M. H., Saia Cereda C. M., Fernandes Fraceto L., de Paula E. Liposomal-based lidocaine formulation for the improvement of infiltrative buccal anaesthesia. Journal of Liposome Research. 2019;29(1),66–72. DOI: 10.1080/08982104.2018.1483947.</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Kent B., Garvey C. J., Cookson D., Bryant G. The inverse hexagonal – inverse ribbon – lamellar gel phase transition sequence in low hydration DOPC:DOPE phospholipid mixtures. Chemistry and Physics of Lipids. 2009;157(1):56–60. DOI: 10.1016/j.chemphyslip.2008.10.003.</mixed-citation><mixed-citation xml:lang="en">Kent B., Garvey C. J., Cookson D., Bryant G. The inverse hexagonal – inverse ribbon – lamellar gel phase transition sequence in low hydration DOPC:DOPE phospholipid mixtures. Chemistry and Physics of Lipids. 2009;157(1):56–60. DOI: 10.1016/j.chemphyslip.2008.10.003.</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Guida V. Thermodynamics and kinetics of vesicles formation processes. Advances in Colloid and Interface Science. 2010;161(1–2):77–88. DOI: 10.1016/j.cis.2009.11.004.</mixed-citation><mixed-citation xml:lang="en">Guida V. Thermodynamics and kinetics of vesicles formation processes. Advances in Colloid and Interface Science. 2010;161(1–2):77–88. DOI: 10.1016/j.cis.2009.11.004.</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Cohen J. A. Electrophoretic characterization of liposomes. Methods in Enzymology. 2003;367:148–176. DOI: 10.1016/S0076-6879(03)67011-4.</mixed-citation><mixed-citation xml:lang="en">Cohen J. A. Electrophoretic characterization of liposomes. Methods in Enzymology. 2003;367:148–176. DOI: 10.1016/S0076-6879(03)67011-4.</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Heurtault B., Saulnier P., Pech B., Proust J.-E., Benoit J.-P. Physico-chemical stability of colloidal lipid particles. Biomaterials. 2003;24(23):4283–4300. DOI: 10.1016/S0142-9612(03)00331-4.</mixed-citation><mixed-citation xml:lang="en">Heurtault B., Saulnier P., Pech B., Proust J.-E., Benoit J.-P. Physico-chemical stability of colloidal lipid particles. Biomaterials. 2003;24(23):4283–4300. DOI: 10.1016/S0142-9612(03)00331-4.</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Стадниченко А. В., Краснопольский Ю. М., Ярных Т. Г. Оптимизация параметров дзета-потенциала при создании липосом с иринотеканом. Фармация Казахстана. 2017;6:7–10.</mixed-citation><mixed-citation xml:lang="en">Stadnichenko A. V., Krasnopol’skij Yu. M., Yarnyh T. G. Optimization of zeta potential parameters when creating liposomes with irinotecan. Farmaciya Kazahstana. 2017;6:7–10. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Стадниченко А. В., Краснопольский Ю. М., Ярных Т. Г. Изучение факторов, влияющих на стабильность липосом с цитостатиками при регидратации. Рецепт. 2017;20(2):146–152.</mixed-citation><mixed-citation xml:lang="en">Stadnichenko A. V., Krasnopol’skij Yu. M., Yarnyh T. G. Study of factors affecting the stability of liposomes with cytostatics during rehydration. Recept. 2017;20(2):146–152. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Гулякин И. Д., Николаева Л. Л., Дмитриева М. В., Оборотова Н. А., Орлова О. Л., Полозкова А. П. Разработка лиофилизированной липосомальной лекарственной формы производного индолокарбазола – ЛХС-1208. Фармацевтическое дело и технология лекарств. 2020;(5):66–78.</mixed-citation><mixed-citation xml:lang="en">Gulyakin I. D., Nikolaeva L. L., Dmitrieva M. V., Oborotova N. A., Orlova O. L., Polozkova A. P. Development of a lyophilized liposomal dosage form of an indolocarbazole derivative – LHS-1208. Pharmaceutical business and drug technology. 2020;(5):66–78. (In Russ.)</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Vélez M. A., Perotti M. C., Hynes E. R., Gennaro A. M. Effect of lyophilization on food grade liposomes loaded with conjugated linoleic acid. Journal of Food Engineering. 2019;240:199–206. DOI: 10.1016/j.jfoodeng.2018.07.033.</mixed-citation><mixed-citation xml:lang="en">Vélez M. A., Perotti M. C., Hynes E. R., Gennaro A. M. Effect of lyophilization on food grade liposomes loaded with conjugated linoleic acid. Journal of Food Engineering. 2019;240:199–206. DOI: 10.1016/j.jfoodeng.2018.07.033.</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">Yadav A. V, Murthy M. S., Shete A. S., Sakhare S. Stability aspects of liposomes. Indian Journal of Pharmaceutical Education and Research. 2011;45(4):402–413.</mixed-citation><mixed-citation xml:lang="en">Yadav A. V, Murthy M. S., Shete A. S., Sakhare S. Stability aspects of liposomes. Indian Journal of Pharmaceutical Education and Research. 2011;45(4):402–413.</mixed-citation></citation-alternatives></ref><ref id="cit85"><label>85</label><citation-alternatives><mixed-citation xml:lang="ru">D’souza A. A., Shegokar R. Polyethylene glycol (PEG): a versatile polymer for pharmaceutical applications. Expert Opinion on Drug Delivery. 2016;13(9):1257–1275. DOI: 10.1080/17425247.2016.1182485.</mixed-citation><mixed-citation xml:lang="en">D’souza A. A., Shegokar R. Polyethylene glycol (PEG): a versatile polymer for pharmaceutical applications. Expert Opinion on Drug Delivery. 2016;13(9):1257–1275. DOI: 10.1080/17425247.2016.1182485.</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>
