<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Genes &amp; Cells</journal-id><journal-title-group><journal-title xml:lang="en">Genes &amp; Cells</journal-title><trans-title-group xml:lang="ru"><trans-title>Гены и Клетки</trans-title></trans-title-group><trans-title-group xml:lang="zh"><trans-title>Genes and Cells</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2313-1829</issn><issn publication-format="electronic">2500-2562</issn><publisher><publisher-name xml:lang="en">Human Stem Cells Institute</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">312198</article-id><article-id pub-id-type="doi">10.23868/gc312198</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Reviews</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Научные обзоры</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Methods for assessing the viability of cells cultured in vitro in 2D and 3D structures</article-title><trans-title-group xml:lang="ru"><trans-title>Методы оценки жизнеспособности клеток, культивируемых in vitro в 2D- и 3D-структурах</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-3428-7586</contrib-id><contrib-id contrib-id-type="spin">4825-5440</contrib-id><name-alternatives><name xml:lang="en"><surname>Eremeev</surname><given-names>Artem V.</given-names></name><name xml:lang="ru"><surname>Еремеев</surname><given-names>Артём Валерьевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Biol.)</p></bio><bio xml:lang="ru"><p>канд. биол. наук</p></bio><email>art-eremeev@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8967-2318</contrib-id><name-alternatives><name xml:lang="en"><surname>Pikina</surname><given-names>Arina S.</given-names></name><name xml:lang="ru"><surname>Пикина</surname><given-names>Арина Сергеевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>arina.pikina@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0001-9266-2065</contrib-id><name-alternatives><name xml:lang="en"><surname>Vladimirova</surname><given-names>Tatyana V.</given-names></name><name xml:lang="ru"><surname>Владимирова</surname><given-names>Татьяна Викторовна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>tat.vlad24@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1549-1984</contrib-id><contrib-id contrib-id-type="spin">8093-8009</contrib-id><name-alternatives><name xml:lang="en"><surname>Bogomazova</surname><given-names>Alexandra N.</given-names></name><name xml:lang="ru"><surname>Богомазова</surname><given-names>Александра Никитична</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Cand. Sci. (Biol.)</p></bio><bio xml:lang="ru"><p>канд. биол. наук</p></bio><email>abogomazova@rcpcm.org</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency</institution></aff><aff><institution xml:lang="ru">Федеральный научно-клинический центр физико-химической медицины имени академика Ю.М. Лопухина Федерального медико-биологического агентства России</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2023-04-11" publication-format="electronic"><day>11</day><month>04</month><year>2023</year></pub-date><pub-date date-type="pub" iso-8601-date="2023-05-28" publication-format="electronic"><day>28</day><month>05</month><year>2023</year></pub-date><volume>18</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>5</fpage><lpage>21</lpage><history><date date-type="received" iso-8601-date="2023-03-05"><day>05</day><month>03</month><year>2023</year></date><date date-type="accepted" iso-8601-date="2023-03-27"><day>27</day><month>03</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2023, Eremeev A.V., Pikina A.S., Vladimirova T.V., Bogomazova A.N.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2023, Еремеев А.В., Пикина А.С., Владимирова Т.В., Богомазова А.Н.</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="en">Eremeev A.V., Pikina A.S., Vladimirova T.V., Bogomazova A.N.</copyright-holder><copyright-holder xml:lang="ru">Еремеев А.В., Пикина А.С., Владимирова Т.В., Богомазова А.Н.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2026-05-28"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by-nc-nd/4.0/</ali:license_ref></license></permissions><self-uri xlink:href="https://genescells.ru/2313-1829/article/view/312198">https://genescells.ru/2313-1829/article/view/312198</self-uri><abstract xml:lang="en"><p>Over the past decades, cell viability tests have been an essential research tool in cell biology, tissue engineering, and regenerative medicine. Assessment of cell viability is mandatory in the production and quality control of cell products for biomedical applications.</p> <p>Methods of viability assessment can be broadly classified according to the underlying mechanism and how the results obtained are evaluated. This article presents variants of the most commonly used tests and protocols for assessing cell viability. Their advantages and disadvantages are presented, which should be considered when planning experiments, e.g., when developing cell preparations for regenerative medicine.</p> <p>The authors point out the main factors influencing the choice of viability assessment method: efficiency, speed, safety, reproducibility, sample integrity, compatibility with biomaterial, and cell line type. Finally, the authors discuss separately cell viability tests that can be applied not only to 2D cell structures but also to 3D cell structures, which have recently become widespread due to more accurate modeling of biological processes.</p></abstract><trans-abstract xml:lang="ru"><p>На протяжении последних десятилетий методы оценки жизнеспособности клеток являются важным исследовательским инструментом в клеточной биологии, тканевой инженерии и регенеративной медицине. Кроме того, оценка жизнеспособности клеток обязательна при производстве и контроле качества клеточных продуктов для биомедицинских нужд.</p> <p>Методы оценки жизнеспособности клеток можно широко классифицировать по механизму, лежащему в их основе, а также по способу оценки полученных результатов. Представлены варианты наиболее часто используемых тестов и протоколов для оценки жизнеспособности клеток. Приведены их преимущества и недостатки, которые необходимо учитывать при планировании экспериментов, например, при разработке клеточных препаратов для регенеративной медицины.</p> <p>Показаны основные факторы, влияющие на выбор метода оценки жизнеспособности клеток: эффективность, быстрота исполнения, безопасность, воспроизводимость, сохранность/целостность образца, совместимость протокола исследования с биоматериалом и типом клеточной линии. Отдельно рассмотрены тесты, которые можно применять не только для 2D-клеточных структур, но и для 3D-клеточных конструкций, получивших в последнее время широкое распространение благодаря более точному моделированию биологических процессов.</p></trans-abstract><kwd-group xml:lang="en"><kwd>viability analysis of cells</kwd><kwd>2D cell structures</kwd><kwd>3D cell structures</kwd><kwd>dye exclusion assay</kwd><kwd>colorimetric method</kwd><kwd>fluorescent dyes</kwd><kwd>luminometric assays</kwd><kwd>flow cytometry</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>анализ жизнеспособности клеток</kwd><kwd>2D-клеточные структуры</kwd><kwd>3D-клеточные структуры</kwd><kwd>анализ исключения красителя</kwd><kwd>колориметрический метод</kwd><kwd>флуоресцентные красители</kwd><kwd>люминометрические анализы</kwd><kwd>проточная цитометрия</kwd></kwd-group><funding-group><funding-statement xml:lang="en">This publication was carried out with state funding for the «Opora-2» project, state registration number of R&amp;D 121101500075-7</funding-statement><funding-statement xml:lang="ru">Данная обзорная публикация выполнена в рамках государственного задания «Опора-2», номер государственного учета НИОКТР 121101500075-7</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Kumar P, Nagarajan A, Uchil PD. Analysis of cell viability by the MTT assay. Cold Spring Harb Protoc. 2018;2018(6). doi: 10.1101/pdb.prot095505</mixed-citation><mixed-citation xml:lang="ru">Kumar P., Nagarajan A., Uchil P.D. Analysis of cell viability by the MTT assay // Cold Spring Harb Protoc. 2018. Vol. 2018, N 6. doi: 10.1101/pdb.prot095505</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Castro-concha LA, Escobedo RM, Miranda-Ham Mde L. Measurement of cell viability. Methods Mol Biol. 2012;877:49–56. doi: 10.1007/978-1-61779-818-4_5</mixed-citation><mixed-citation xml:lang="ru">Castro-concha L.A., Escobedo R.M., Miranda-Ham Mde L. Measurement of cell viability // Methods Mol Biol. 2012. Vol. 877. P. 49–56. doi: 10.1007/978-1-61779-818-4_5</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Kabakov AE, Gabai VL. Cell death and survival assays. Methods Mol Biol. 2018;1709:107–127. doi: 10.1007/978-1-4939-7477-1_9</mixed-citation><mixed-citation xml:lang="ru">Kabakov E., Gabai V.L. Cell death and survival assays // Methods Mol Biol. 2018. Vol. 1709. P. 107–127. doi: 10.1007/978-1-4939-7477-1_9</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Kamiloglu S, Sari G, Ozdal T, Capanoglu E. Guidelines for cell viability assays. Food Frontiers. 2020;1(3):332–349. doi: 10.1002/fft2.44</mixed-citation><mixed-citation xml:lang="ru">Kamiloglu S., Sari G., Ozdal T., Capanoglu E. Guidelines for cell viability assays // Food Frontiers. 2020. Vol. 1, N 3. P. 332–349. doi: 10.1002/fft2.44</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">Strober W. Trypan blue exclusion test of cell viability. Curr Protoc Immunol. 2001; Suppl. 3:3B. doi: 10.1002/0471142735.ima03bs21</mixed-citation><mixed-citation xml:lang="ru">Strober W. Trypan Blue exclusion test of cell viability // Curr Protoc Immunol. 2001. Suppl 3. P. 3B. doi: 10.1002/0471142735.ima03bs21</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Huang CN, Cornejo MJ, Bush DS, Jones RL. Estimating viability of plant protoplasts using double and single staining. Protoplasma. 1986;135:80–87. doi: 10.1007/BF01277001</mixed-citation><mixed-citation xml:lang="ru">Huang C.N., Cornejo M.J., Bush D.S., Jones R.L. Estimating viability of plant protoplasts using double and single staining // Protoplasma. 1986. Vol. 135. P. 80–87. doi: 10.1007/BF01277001</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Babakhanova G, Zimmerman SM, Pierce LT, et al. Quantitative, traceable determination of cell viability using absorbance microscopy. PLoS One. 2022;17(1):e0262119. doi: 10.1371/journal.pone.0262119</mixed-citation><mixed-citation xml:lang="ru">Babakhanova G., Zimmerman S.M., Pierce L.T., et al. Quantitative, traceable determination of cell viability using absorbance microscopy // PLoS One. 2022. Vol. 17, N 1. P. e0262119. doi: 10.1371/journal.pone.0262119</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Alamoudi WA, Ahmad F, Acharya S, et al. A simplified colorimetric method for rapid detection of cell viability and toxicity in adherent cell culture systems. J BUON. 2018;23(5):1505–1513.</mixed-citation><mixed-citation xml:lang="ru">Alamoudi W.A., Ahmad F., Acharya S. A simplified colorimetric method for rapid detection of cell viability and toxicity in adherent cell culture systems // J BUON. 2018. Vol. 23, N 5. P. 1505–1513.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Boncler M, Rózalski M, Krajewska U, et al. Comparison of PrestoBlue and MTT assays of cellular viability in the assessment of anti-proliferative effects of plant extracts on human endothelial cells. J Pharmacol Toxicol Methods. 2014;69(1):9–16. doi: 10.1016/j.vascn.2013.09.003</mixed-citation><mixed-citation xml:lang="ru">Boncler M., Rózalski M., Krajewska U., et al. Comparison of PrestoBlue and MTT assays of cellular viability in the assessment of anti-proliferative effects of plant extracts on human endothelial cells // J Pharmacol Toxicol Methods. 2014. Vol. 69, N 1. P. 9–16. doi: 10.1016/j.vascn.2013.09.003</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">Bopp SK, Lettieri T. Comparison of four different colorimetric and fluorometric cytotoxicity assays in a zebrafish liver cell line. BMC Pharmacol. 2008;8:8. doi: 10.1186/1471-2210-8-8</mixed-citation><mixed-citation xml:lang="ru">Bopp S.K., Lettieri T. Comparison of four different colorimetric and fluorometric cytotoxicity assays in a zebrafish liver cell line // BMC Pharmacol. 2008. Vol. 8. P. 8. doi: 10.1186/1471-2210-8-8</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">Cory AH, Owen TC, Barltrop JA, Cory JG. Use of an aqueous soluble tetrazolium/formazan assay for cell growth assays in culture. Cancer Commun. 1991;3(7):207–212. doi: 10.3727/095535491820873191</mixed-citation><mixed-citation xml:lang="ru">Cory H., Owen T.C., Barltrop J.A., Cory J.G. Use of an aqueous soluble tetrazolium/formazan assay for cell growth assays in culture // Cancer Commun. 1991. Vol. 3, N 7. P. 207–212. doi: 10.3727/095535491820873191</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Goodwin CJ, Holt SJ, Downes S, Marshall NJ. Microculture tetrazolium assays: a comparison between two new tetrazolium salts, XTT and MTS. J Immunol Methods. 1995;179(1):95–103. doi: 10.1016/0022-1759(94)00277-4</mixed-citation><mixed-citation xml:lang="ru">Goodwin J., Holt S.J., Downes S., Marshall N.J. Microculture tetrazolium assays: a comparison between two new tetrazolium salts, XTT and MTS // J Immunol Methods. 1995. Vol. 179. P. 95–103. doi: 10.1016/0022-1759(94)00277-4</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">Lutter AH, Scholka J, Richter H, Anderer U. Applying XTT, WST-1, and WST-8 to human chondrocytes: a comparison of membrane-impermeable tetrazolium salts in 2D and 3D cultures. Clin Hemorheol Microcirc. 2017;67(3-4):327–342. doi: 10.3233/CH-179213</mixed-citation><mixed-citation xml:lang="ru">Lutter A.H., Scholka J., Richter H., Anderer U. Applying XTT, WST-1, and WST-8 to human chondrocytes: a comparison of membrane-impermeable tetrazolium salts in 2D and 3D cultures // Clin Hemorheol Microcirc. 2017. Vol. 67, N 3-4. P. 327–342. doi: 10.3233/CH-179213</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983;65:55–63. doi: 10.1016/0022-1759(83)90303-4</mixed-citation><mixed-citation xml:lang="ru">Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays // J Immunol Methods. 1983. Vol. 65. P. 55–63. doi: 10.1016/0022-1759(83)90303-4</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">Präbst K, Engelhardt H, Ringgeler S, Hübner H. Basic colorimetric proliferation assays: MTT, WST, and Resazurin: basic color prolif assays MTT, WST, Resazurin. Methods Mol Biol. 2017;1601:1–17. doi: 10.1007/978-1-4939-6960-9_1</mixed-citation><mixed-citation xml:lang="ru">Präbst K., Engelhardt H., Ringgeler S., Hübner H. Basic colorimetric proliferation assays: MTT, WST, and Resazurin: basic color prolif assays MTT, WST, Resazurin // Methods Mol Biol. 2017. Vol. 1601. P. 1–17. doi: 10.1007/978-1-4939-6960-9_1</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">Hall MD, Martin C, Ferguson DJ, et al. Comparative efficacy of novel platinum (IV) compounds with established chemotherapeutic drugs in solid tumour models. Biochem Pharmacol. 2004;67(1):17–30. doi: 10.1016/j.bcp.2003.07.016</mixed-citation><mixed-citation xml:lang="ru">Hall M.D., Martin C., Ferguson D.J., et al. Comparative efficacy of novel platinum (IV) compounds with established chemotherapeutic drugs in solid tumour models // Biochem Pharmacol. 2004. Vol. 67, N 1. P. 17–30. doi: 10.1016/j.bcp.2003.07.016</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">Berridge MV, Tan AS. Characterization of the cellular reduction of (MTT) subcellular localization, substrate dependence, and involvement of mitochondrial electron transport in MTT reduction. Arch Biochem Biophys. 1993;303(2):474–482. doi: 10.1006/abbi.1993.1311</mixed-citation><mixed-citation xml:lang="ru">Berridge M.V., Tan A.S. Characterization of the cellular reduction of (MTT) subcellular localization, substrate dependence, and involvement of mitochondrial electron transport in MTT reduction // Arch Biochem Biophys. 1993. Vol. 303, N 2. P. 474–482. doi: 10.1006/abbi.1993.1311</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">Bernas T, Dobrucki J. Mitochondrial and nonmitochondrial reduction of MTT: interaction of MTT with TMRE, JC-1, and NAO mitochondrial fluorescent probes. Cytometry. 2002;47(4):236–242. doi: 10.1002/cyto.10080</mixed-citation><mixed-citation xml:lang="ru">Bernas T., Dobrucki J. Mitochondrial and nonmitochondrial reduction of MTT: interaction of MTT with TMRE, JC-1, and NAO mitochondrial fluorescent probes // Cytometry. 2002. Vol. 47, N 4. P. 236–242. doi: 10.1002/cyto.10080</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">Chakrabarti R, Kundu S, Kumar S, Chakrabarti R. Vitamin A as an enzyme that catalyzes the reduction of MTT to formazan by vitamin C. J Cell Biochem. 2000;80(1):133–138. doi: 10.1002/1097-4644(20010101)80:1&lt;133::AID-JCB120&gt;3.0.CO;2-T</mixed-citation><mixed-citation xml:lang="ru">Chakrabarti R., Kundu S., Kumar S., Chakrabarti R. Vitamin A as an enzyme that catalyzes the reduction of MTT to formazan by vitamin C // J Cell Biochem. 2000. Vol. 80, N 1. P. 133–138. doi: 10.1002/1097-4644(20010101)80:1&lt;133::AID-JCB120&gt;3.0.CO;2-T</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">Collier AC, Pritsos CA. The mitochondrial uncoupler dicumarol disrupts the MTT assay. Biochem Pharmacol. 2003;66(2):281–287. doi: 10.1016/S0006-2952(03)00240-5</mixed-citation><mixed-citation xml:lang="ru">Collier C., Pritsos C.A. The mitochondrial uncoupler dicumarol disrupts the MTT assay // Biochem Pharmacol. 2003. Vol. 66, N 2. P. 281–287. doi: 10.1016/S0006-2952(03)00240-5</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">Ulukaya E, Colakogullari M, Wood EJ. Interference by anti-cancer chemotherapeutic agents in the MTT-tumor chemosensitivity assay. Chemotherapy. 2004;50(1):43–50. doi: 10.1159/000077285</mixed-citation><mixed-citation xml:lang="ru">Ulukaya E., Colakogullari M., Wood E.J. Interference by anti-cancer chemotherapeutic agents in the MTT-tumor chemosensitivity assay // Chemotherapy. 2004. Vol. 50, N 1. P. 43–50. doi: 10.1159/000077285</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">Vistica DT, Skehan P, Scudiero D, et al. Tetrazolium-based assays for cellular viability: a critical examination of selected parameters affecting formazan production. Cancer Res. 1991;51(10):2515–2520.</mixed-citation><mixed-citation xml:lang="ru">Vistica D.T., Skehan P., Scudiero D., et al. Tetrazolium-based assays for cellular viability: a critical examination of selected parameters affecting formazan production // Cancer Res. 1991. Vol. 51, N 10. P. 2515–2520.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><mixed-citation>Promega Corporation. CellTiter 96® Non-Radioactive Cell Proliferation Assay. Insructions use of products G4000 and G41000. Technical Bulletin. USA, 2012.</mixed-citation></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">Lü L, Zhang L, Sen M, et al. Toxicology in vitro exocytosis of MTT formazan could exacerbate cell injury. Toxicol In Vitro. 2012;26(4):636–644. doi: 10.1016/j.tiv.2012.02.006</mixed-citation><mixed-citation xml:lang="ru">Lü L., Zhang L., Mun Wai M., et al. Toxicology in vitro exocytosis of MTT formazan could exacerbate cell injury // Toxicol In Vitro. 2012. Vol. 26, N 4. P. 636–644. doi: 10.1016/j.tiv.2012.02.006</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">Riss TL, Moravec RA, Niles AL, et al. Cell viability assays. Assay Guid Man. 2004:1–25.</mixed-citation><mixed-citation xml:lang="ru">Riss T.L., Moravec R.A., Niles A.L., et al. Cell viability assays // Assay Guid Man. 2004. C. 1–25.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">Berridge MV, Herst PM, Tan AS. Tetrazolium dyes as tools in cell biology: new insights into their cellular reduction. Biotechnol Annu Rev. 2005;11:127–152. doi: 10.1016/S1387-2656(05)11004-7</mixed-citation><mixed-citation xml:lang="ru">Berridge M.V., Herst P.M., Tan A.S. Tetrazolium dyes as tools in cell biology: new insights into their cellular reduction // Biotechnol Annu Rev. 2005. Vol. 11. P. 127–152. doi: 10.1016/S1387-2656(05)11004-7</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">Repetto G, del Peso A, Zurita JL. Neutral red uptake assay for the estimation of cell viability/cytotoxicity. Nat Protoc. 2008;3(7):1125–1131. doi: 10.1038/nprot.2008.75</mixed-citation><mixed-citation xml:lang="ru">Repetto G., del Peso A., Zurita J.L. Neutral red uptake assay for the estimation of cell viability/cytotoxicity // Nat Protoc. 2008. Vol. 3, N 7. P. 1125–1131. doi: 10.1038/nprot.2008.75</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">Gomez-Gutierrez JG, Bhutiani N, Mcnally MW, et al. During autophagy or in an acidic microenvironment in vitro. Biotech Histochem. 2022;96(4):302–310. doi: 10.1080/10520295.2020.1802065</mixed-citation><mixed-citation xml:lang="ru">Gomez-gutierrez J.G., Bhutiani N., McNally M.W., et al. During autophagy or in an acidic microenvironment in vitro // Biotech Histochem. 2022. Vol. 96, N 4. P. 302–310. doi: 10.1080/10520295.2020.1802065</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">Altman SA, Randers L, Rao G. Comparison of Trypan blue dye exclusion and fluorometric assays for mammalian cell viability determinations. Biotechnol Prog. 1993;9(6):671–674. doi: 10.1021/bp00024a017</mixed-citation><mixed-citation xml:lang="ru">Altman S.A., Randers L., Rao G. Comparison of Trypan Blue dye exclusion and fluorometric assays for mammalian cell viability determinations // Biotechnol Prog. 1993. Vol. 9, N 6. P. 671–674. doi: 10.1021/bp00024a017</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">Shum D, Radu C, Kim E, et al. A high density assay format for the detection of novel cytotoxic agents in large chemical libraries. J Enzyme Inhib Med Chem. 2008;23(6):931–945. doi: 10.1080/14756360701810082</mixed-citation><mixed-citation xml:lang="ru">Shum D., Radu C., Kim E., et al. A high density assay format for the detection of novel cytotoxic agents in large chemical libraries // J Enzyme Inhib Med Chem. 2008. Vol. 23, N 6. P. 931–945. doi: 10.1080/14756360701810082</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">O’Brien J, Wilson I, Orton T, Pognan F. Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity. Eur J Biochem. 2000;267(17):5421–5426. doi: 10.1046/j.1432-1327.2000.01606.x</mixed-citation><mixed-citation xml:lang="ru">O’Brien O., Wilson I., Orton T., Pognan F. Investigation of the Alamar Blue (resazurin) fluorescent dye for the assessment of mammalian cell cytotoxicity // Eur J Biochem. 2000. Vol. 267, N 17. P. 5421–5426. doi: 10.1046/j.1432-1327.2000.01606.x</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">Luzak B, Siarkiewicz P, Boncler M. An evaluation of a new high-sensitivity PrestoBlue assay for measuring cell viability and drug cytotoxicity using EA.hy926 endothelial cells. Toxicol In Vitro. 2022;83:105407. doi: 10.1016/j.tiv.2022.105407</mixed-citation><mixed-citation xml:lang="ru">Luzak B., Siarkiewicz P., Boncler M. An evaluation of a new high-sensitivity PrestoBlue assay for measuring cell viability and drug cytotoxicity using EA.hy926 endothelial cells // Toxicol In Vitro. 2022. Vol. 83. P. 105407. doi: 10.1016/j.tiv.2022.105407</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">Ahmed SA, Gogal RM, Walsh JE. A new rapid and simple non-radioactive assay to monitor and determine the proliferation of lymphocytes: an alternative to [3H] thymidine incorporation assay. J Immunol Methods. 1994;170(2):211–224. doi: 10.1016/0022-1759(94)90396-4</mixed-citation><mixed-citation xml:lang="ru">Ahmed S.A., Gogal R.M., Walsh J.E. A new rapid and simple non-radioactive assay to monitor and determine the proliferation of lymphocytes: an alternative to [3H] thymidine incorporation assay // J Immunol Methods. 1994. Vol. 170, N 2. P. 211–224. doi: 10.1016/0022-1759(94)90396-4</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">Lavogina D, Lust H, Tahk MJ, et al. Revisiting the Resazurin-based sensing of cellular viability: widening the application horizon. Biosensors (Basel). 2022;12(4):196. doi: 10.3390/bios12040196</mixed-citation><mixed-citation xml:lang="ru">Lavogina D., Lust H., Tahk M.J., et al. Revisiting the Resazurin-based sensing of cellular viability: widening the application horizon // Biosensors (Basel). 2022. Vol. 12, N 4. P. 196. doi: 10.3390/bios12040196</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">Patent USA N 5501959/26.03.1996. Lancaster MV, Fields RD. Antibiotic and cytotoxic drug susceptibility assays using resazurin and poising agents. Available from: https://patentimages.storage.googleapis.com/e5/b8/74/fadfc8c037ebbc/US5501959.pdf</mixed-citation><mixed-citation xml:lang="ru">Patent USA N 5501959/26.03.1996. Lancaster M.V., Fields R.D. Antibiotic and cytotoxic drug susceptibility assays using resazurin and poising agents. Режим доступа: https://patentimages.storage.googleapis.com/e5/b8/74/fadfc8c037ebbc/US5501959.pdf</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">https://www.thermofisher.com/ [Internet]. Invitrogen Corporation. AlamarBlue™ HS cell viability reagent. Available from: https://www.thermofisher.com/order/catalog/product/A50100</mixed-citation><mixed-citation xml:lang="ru">https://www.thermofisher.com/ [Internet]. Invitrogen Corporation. AlamarBlue™ HS cell viability reagent. Доступ по ссылке: https://www.thermofisher.com/order/catalog/product/A50100</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">Voytik-Harbin SL, Brightman AO, Waisner B, et al. Application and evaluation of the alamarblue assay for cell growth and survival of fibroblasts. In Vitro Cell Dev Biol Anim. 1998;34(3):239–246. doi: 10.1007/s11626-998-0130-x</mixed-citation><mixed-citation xml:lang="ru">Voytik-Harbin S.L., Brightman A.O., Waisner B., et al. Application and evaluation of the alamarblue assay for cell growth and survival of fibroblasts // In Vitro Cell Dev Biol Anim. 1998. Vol. 34, N 3. P. 239–246. doi: 10.1007/s11626-998-0130-x</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">Nakayama GR, Caton MC, Nova MP, Parandoosh Z. Assessment of the Alamar Blue assay for cellular growth and viability in vitro. J Immunol Methods. 1997;204(2):205–208. doi: 10.1016/S0022-1759(97)00043-4</mixed-citation><mixed-citation xml:lang="ru">Nakayama G.R., Caton M.C., Nova M.P., Parandoosh Z. Assessment of the Alamar Blue assay for cellular growth and viability in vitro // J Immunol Methods. 1997. Vol. 204, N 2. P. 205–208. doi: 10.1016/S0022-1759(97)00043-4</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">Hamid R, Rotshteyn Y, Rabadi L, et al. Comparison of Alamar Blue and MTT assays for high through-put screening. Toxicol In Vitro. 2004;18(5):703–710. doi: 10.1016/j.tiv.2004.03.012</mixed-citation><mixed-citation xml:lang="ru">Hamid R., Rotshteyn Y., Rabadi L., et al. Comparison of alamar blue and MTT assays for high through-put screening // Toxicol in Vitro. 2004. Vol. 18, N 5. P. 703–710. doi: 10.1016/j.tiv.2004.03.012</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">Shahan TA, Siegel PD, Sorenson WG, et al. A sensitive new bioassay for tumor necrosis factor. J Immunol Methods. 1994;175(2):181–187. doi: 10.1016/0022-1759(94)90361-1</mixed-citation><mixed-citation xml:lang="ru">Shahan T.A., Siegel P.D., Sorenson W.G., et al. A sensitive new bioassay for tumor necrosis factor // J Immunol Methods. 1994. Vol. 175, N 2. P. 181–187. doi: 10.1016/0022-1759(94)90361-1</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">Dayeh VR, Bols NC, Schirmer K. The use of fish-derived cell lines for investigation of environmental contaminants: an update following OECD’s fish toxicity testing framework No. 171. Curr Protoc Toxicol. 2013;Chapter 1:Unit1.5. doi: 10.1002/0471140856.tx0105s56</mixed-citation><mixed-citation xml:lang="ru">Dayeh V.R., Bols N.C., Schirmer K. The use of fish-derived cell lines for investigation of environmental contaminants: an update following OECD’s fish toxicity testing framework No. 171 // Curr Protoc Toxicol. 2013. Chapter 1. Unit1.5. doi: 10.1002/0471140856.tx0105s56</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">White MJ, DiCaprio MJ, Greenberg DA. Assessment of neuronal viability with Alamar blue in cortical and granule cell cultures. J Neurosci Methods. 1996;70(2):195–200. doi: 10.1016/S0165-0270(96)00118-5</mixed-citation><mixed-citation xml:lang="ru">White M.J., DiCaprio M.J., Greenberg D.A. Assessment of neuronal viability with Alamar blue in cortical and granule cell cultures // J Neurosci Methods. 1996. Vol. 70, N 2. P. 195–200. doi: 10.1016/S0165-0270(96)00118-5</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">Yu SY, Sales KM, Fuller BJ, et al. Inducing apoptosis of human colon cancer cells by an IGF-I D domain analogue peptide. Mol Cancer. 2008;7:17. doi: 10.1186/1476-4598-7-17</mixed-citation><mixed-citation xml:lang="ru">Yu S.Y., Sales K.M., Fuller B.J., et al. Inducing apoptosis of human colon cancer cells by an IGF-I D domain analogue peptide // Mol Cancer. 2008. Vol. 7. P. 17. doi: 10.1186/1476-4598-7-17</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">Yajko DM, Madej JJ, Lancaster MV, et al. Colorimetric method for determining MICs of antimicrobial agents for Mycobacterium tuberculosis. J Clin Microbiol. 1995;33(9):2324–2327. doi: 10.1128/jcm.33.9.2324-2327.1995</mixed-citation><mixed-citation xml:lang="ru">Yajko M., Madej J.J., Lancaster M.V., et al. Colorimetric method for determining MICs of antimicrobial agents for Mycobacterium tuberculosis // J Clin Microbiol. 1995. Vol. 33, N 9. P. 2324–2327. doi: 10.1128/jcm.33.9.2324-2327.1995</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">Xu M, Mccanna DJ, Sivak JG. Use of the viability reagent PrestoBlue in comparison with alamarBlue and MTT to assess the viability of human corneal epithelial cells. J Pharmacol Toxicol Methods. 2015;71:1–7. doi: 10.1016/j.vascn.2014.11.003</mixed-citation><mixed-citation xml:lang="ru">Xu M., Mccanna D.J., Sivak J.G. Use of the viability reagent PrestoBlue in comparison with alamarBlue and MTT to assess the viability of human corneal epithelial cells // J Pharmacol Toxicol Methods. 2015. Vol. 71. P. 1–7. doi: 10.1016/j.vascn.2014.11.003</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">Yu HG, Chung H, Yu YS, et al. A new rapid and non-radioactive assay for monitoring and determining the proliferation of retinal pigment epithelial cells. Korean J Ophthalmol. 2003;17(1):29–34. doi: 10.3341/kjo.2003.17.1.29</mixed-citation><mixed-citation xml:lang="ru">Yu H.G., Chung H., Yu Y.S., et al. A new rapid and non-radioactive assay for monitoring and determining the proliferation of retinal pigment epithelial cells // Korean J Ophthalmol. 2003. Vol. 17, N 1. P. 29–34. doi: 10.3341/kjo.2003.17.1.29</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">Niles AL, Moravec RA, Hesselberth P, et al. A homogeneous assay to measure live and dead cells in the same sample by detecting different protease markers. Anal Biochem. 2007;366:197–206. doi: 10.1016/j.ab.2007.04.007</mixed-citation><mixed-citation xml:lang="ru">Niles L., Moravec R.A., Hesselberth P., et al. A homogeneous assay to measure live and dead cells in the same sample by detecting different protease markers // Anal Biochem. 2007. Vol. 366. P. 197–206. doi: 10.1016/j.ab.2007.04.007</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">https://assets.thermofisher.com/ [Internet]. Invitrogen. PrestoBlue® cell viability reagent. Available from: https://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0018370-PrestoBlueCellViabilityReagent-PI.pdf</mixed-citation><mixed-citation xml:lang="ru">https://assets.thermofisher.com/ [Internet]. Invitrogen. PrestoBlue® Cell Viability Reagent. Режим доступа: https://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0018370-PrestoBlueCellViabilityReagent-PI.pdf</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">Richards R, Honeywell ME, Lee MJ. FLICK: an optimized plate reader-based assay to infer cell death kinetics. STAR Protoc. 2021;2(1):100327. doi: 10.1016/j.xpro.2021.100327</mixed-citation><mixed-citation xml:lang="ru">Richards R., Honeywell M.E., Lee M.J. FLICK: an optimized plate reader-based assay to infer cell death kinetics // STAR Protoc. 2021. Vol. 2, N 1, P. 100327. doi: 10.1016/j.xpro.2021.100327</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">Yang N, Hui W, Dong S, et al. Temperature tolerance electric cell-substrate impedance sensing for joint assessment of cell viability and vitality. ACS Sens. 2021;6(10):3640–3649. doi: 10.1021/acssensors.1c01211</mixed-citation><mixed-citation xml:lang="ru">Yang N., Hui W., Dong S., et al. Temperature tolerance electric cell-substrate impedance sensing for joint assessment of cell viability and vitality // ACS Sens. 2021. Vol. 6, N 10. P. 3640–3649. doi: 10.1021/acssensors.1c01211</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">Lundin A. Use of firefly luciferase in ATP-related assays of biomass, enzymes, and metabolites. Methods Enzymol. 2000;305(1975):346–370. doi: 10.1016/s0076-6879(00)05499-9</mixed-citation><mixed-citation xml:lang="ru">Lundin A. Use of firefly luciferase in ATP-related assays of biomass, enzymes, and metabolites // Methods Enzymol. 2001. Vol. 305, N 1975. P. 346–370. doi: 10.1016/s0076-6879(00)05499-9</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">Auld DS, Zhang YQ, Southall NT, et al. A basis for reduced chemical library inhibition of firefly luciferase obtained from directed evolution. J Med Chem. 2009;52(5):1450–1458. doi: 10.1021/jm8014525</mixed-citation><mixed-citation xml:lang="ru">Auld S., Zhang Y.Q., Southall N.T., et al. A basis for reduced chemical library inhibition of firefly luciferase obtained from directed evolution // J Med Chem. 2009. Vol. 52, N 5. P. 1450–1458. doi: 10.1021/jm8014525</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">Promega Corporation. CellTiter-Glo® luminescent cell viability assay. [Internet]. Madison, USA, 2023. Available from: https://worldwide.promega.com/-/media/files/resources/protocols/technical-bulletins/0/celltiter-glo-luminescent-cell-viability-assay-protocol.pdf?rev=0d95c232094b41daa06d0c110d1d916f&amp;sc_lang=en</mixed-citation><mixed-citation xml:lang="ru">Promega Corporation. CellTiter-Glo® luminescent cell viability assay. [Internet]. Madison, USA, 2023. Доступ по ссылке: https://worldwide.promega.com/-/media/files/resources/protocols/technical-bulletins/0/celltiter-glo-luminescent-cell-viability-assay-protocol.pdf?rev=0d95c232094b41daa06d0c110d1d916f&amp;sc_lang=en</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">https://worldwide.promega.com/ [Internet]. RealTime-GloTM MT Cell Viability Assay. Available from: https://no.promega.com/products/cell-health-assays/cell-viability-and-cytotoxicity-assays/realtime_glo-mt-cell-viability-assay/?catNum=G9711</mixed-citation><mixed-citation xml:lang="ru">https://worldwide.promega.com/ [Internet]. RealTime-GloTM MT Cell Viability Assay. Доступ по ссылке: https://no.promega.com/products/cell-health-assays/cell-viability-and-cytotoxicity-assays/realtime_glo-mt-cell-viability-assay/?catNum=G9711</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">Duellman SJ, Zhou W, Meisenheimer P, et al. Bioluminescent, nonlytic, real-time cell viability assay and use in inhibitor screening. Assay Drug Dev Technol. 2015;13(8):456–465. doi: 10.1089/adt.2015.669</mixed-citation><mixed-citation xml:lang="ru">Duellman S.J., Zhou W., Meisenheimer P., et al. Bioluminescent, nonlytic, real-time cell viability assay and use in inhibitor screening // Assay Drug Dev Technol. 2015. Vol. 13, N 8. P. 456–465. doi: 10.1089/adt.2015.669</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">Ibrahim SF, van den Engh G. Flow cytometry and cell sorting. Adv Biochem Eng Biotechnol. 2007;106:19–39. doi: 10.1007/10_2007_073</mixed-citation><mixed-citation xml:lang="ru">Ibrahim S.F., van den Engh G. Flow cytometry and cell sorting // Adv Biochem Eng Biotechnol. 2007. Vol. 106. P. 19–39. doi: 10.1007/10_2007_073</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">Mckinnon KM. Flow cytometry: an overview. Curr Protoc Immunol. 2018;120:5.1.1–5.1.11. doi: 10.1002/cpim.40</mixed-citation><mixed-citation xml:lang="ru">Mckinnon K.M. Flow cytometry: an overview // Curr Protoc Immunol. 2018. Vol. 120. P. 5.1.1–5.1.11. doi: 10.1002/cpim.40</mixed-citation></citation-alternatives></ref><ref id="B58"><label>58.</label><citation-alternatives><mixed-citation xml:lang="en">Wagner T, Guber SE, Stubenrauch ML, et al. Low propidium iodide intensity in flow cytometric white blood cell counting as a marker of cell destruction? Transfusion. 2005;45(2):228–233. doi: 10.1111/j.1537-2995.2004.04213.x</mixed-citation><mixed-citation xml:lang="ru">Wagner T., Guber S.E., Stubenrauch M.L. Low propidium iodide intensity in flow cytometric white blood cell counting as a marker of cell destruction? // Transfusion. 2005. Vol. 45, N 2. 228–233. doi: 10.1111/j.1537-2995.2004.04213.x</mixed-citation></citation-alternatives></ref><ref id="B59"><label>59.</label><citation-alternatives><mixed-citation xml:lang="en">Moravvej H, Memariani H, Memariani M, et al. Evaluation of fibroblast viability seeded on acellular human amniotic membrane. Biomed Res Int. 2021;2021:5597758. doi: 10.1155/2021/5597758</mixed-citation><mixed-citation xml:lang="ru">Moravvej H., Memariani H., Memariani M., et al. Evaluation of fibroblast viability seeded on acellular human amniotic membrane // Biomed Res Int. 2021. Vol. 2021. P. 5597758. doi: 10.1155/2021/5597758</mixed-citation></citation-alternatives></ref><ref id="B60"><label>60.</label><citation-alternatives><mixed-citation xml:lang="en">https://www.thermofisher.com/ [Internet]. ThermoFisher Scientific. DAPI (4´,6-diamidino-2-phenylindole). Available from: https://www.thermofisher.com/ru/ru/home/life-science/cell-analysis/fluorophores/dapi-stain.html</mixed-citation><mixed-citation xml:lang="ru">https://www.thermofisher.com/ [Internet]. ThermoFisher Scientific. DAPI (4´,6-diamidino-2-phenylindole). Доступ по ссылке: https://www.thermofisher.com/ru/ru/home/life-science/cell-analysis/fluorophores/dapi-stain.html</mixed-citation></citation-alternatives></ref><ref id="B61"><label>61.</label><citation-alternatives><mixed-citation xml:lang="en">Richards R, Schwartz HR, Honeywell ME. Drug antagonism and single agent dominance result from differences in death kinetics. Nat Chem Biol. 2020;16(7):791–800. doi: 10.1038/s41589-020-0510-4</mixed-citation><mixed-citation xml:lang="ru">Richards R., Schwartz H.R., Honeywell M.E. Drug antagonism and single agent dominance result from differences in death kinetics // Nat Chem Biol. 2020. Vol. 16, N 7. P. 791–800. doi: 10.1038/s41589-020-0510-4</mixed-citation></citation-alternatives></ref><ref id="B62"><label>62.</label><citation-alternatives><mixed-citation xml:lang="en">Masuda S, Shimizu S, Matsuo J, et al. Measurement of NET formation in vitro and in vivo by flow cytometry. Cytom Part A. 2017;91(8):822–829. doi: 10.1002/cyto.a.23169</mixed-citation><mixed-citation xml:lang="ru">Masuda S., Shimizu S., Matsuo J., et al. Measurement of NET formation in vitro and in vivo by flow cytometry // Cytom Part A. 2017. Vol. 91, N 8. P. 822–829. doi: 10.1002/cyto.a.23169</mixed-citation></citation-alternatives></ref><ref id="B63"><label>63.</label><citation-alternatives><mixed-citation xml:lang="en">Zhong J, Yang D, Zhou Y, et al. Multi-frequency single cell electrical impedance measurement for label-free cell viability analysis. Analyst. 2021;146(6):1848–1858. doi: 10.1039/d0an02476g</mixed-citation><mixed-citation xml:lang="ru">Zhong J., Yang D., Zhou Y., et al. Multi-frequency single cell electrical impedance measurement for label-free cell viability analysis // Analyst. 2021. Vol. 146, N 6, P. 1848–1858. doi: 10.1039/d0an02476g</mixed-citation></citation-alternatives></ref><ref id="B64"><label>64.</label><citation-alternatives><mixed-citation xml:lang="en">https://d1spbj2x7qk4bg.cloudfront.net/ [Internet]. BioLegend Corporation. Zombie NIR™ Fixable Viability Kit. Available from: https://d1spbj2x7qk4bg.cloudfront.net/fr-lu/products/zombie-nir-fixable-viability-kit-8657?pdf=true&amp;displayInline=true&amp;leftRightMargin=15&amp;topBottomMargin=15&amp;filename=Zombie%20NIR%E2%84%A2%20Fixable%20Viability%20Kit.pdf&amp;v=20220831123135</mixed-citation><mixed-citation xml:lang="ru">https://d1spbj2x7qk4bg.cloudfront.net/ [Internet]. BioLegend Corporation. Zombie NIR™ Fixable Viability Kit. Доступ по ссылке: https://d1spbj2x7qk4bg.cloudfront.net/fr-lu/products/zombie-nir-fixable-viability-kit-8657?pdf=true&amp;displayInline=true&amp;leftRightMargin=15&amp;topBottomMargin=15&amp;filename=Zombie%20NIR%E2%84%A2%20Fixable%20Viability%20Kit.pdf&amp;v=20220831123135</mixed-citation></citation-alternatives></ref><ref id="B65"><label>65.</label><citation-alternatives><mixed-citation xml:lang="en">https://www.thermofisher.com/ [Internet]. ThermoFisher Scientific. Live/Dead cell viability assays. Available from: https://www.thermofisher.com/ru/ru/home/life-science/cell-analysis/cell-viability-and-regulation/cell-viability/live-dead-cell-viability-assays.html</mixed-citation><mixed-citation xml:lang="ru">https://www.thermofisher.com/ [Internet]. ThermoFisher Scientific. Live/Dead cell viability assays. Доступ по ссылке: https://www.thermofisher.com/ru/ru/home/life-science/cell-analysis/cell-viability-and-regulation/cell-viability/live-dead-cell-viability-assays.html</mixed-citation></citation-alternatives></ref><ref id="B66"><label>66.</label><citation-alternatives><mixed-citation xml:lang="en">https://www.bdbiosciences.com/ [Internet]. BD Biosciences. Fixable Viability Stain 780. Available from: https://www.bdbiosciences.com/content/bdb/paths/generate-tds-document.au.565388.pdf</mixed-citation><mixed-citation xml:lang="ru">https://www.bdbiosciences.com/ [Internet]. BD Biosciences. Fixable Viability Stain 780. Доступ по ссылке: https://www.bdbiosciences.com/content/bdb/paths/generate-tds-document.au.565388.pdf</mixed-citation></citation-alternatives></ref><ref id="B67"><label>67.</label><citation-alternatives><mixed-citation xml:lang="en">Madorran E, Stožer A, Arsov Z, et al. A promising method for the determination of cell viability: the membrane potential cell viability assay. Cells. 2022;11(15):2314. doi: 10.3390/cells11152314</mixed-citation><mixed-citation xml:lang="ru">Madorran E., Stožer A., Arsov Z., et al. A promising method for the determination of cell viability: the membrane potential cell viability assay // Cells. 2022. Vol. 11, N 15. P. 2314. doi: 10.3390/cells11152314</mixed-citation></citation-alternatives></ref><ref id="B68"><label>68.</label><citation-alternatives><mixed-citation xml:lang="en">Zhang R, Wei M, Chen S, et al. A cell viability assessment method based on area-normalized impedance spectrum (ANIS). Biosens Bioelectron. 2018;110:193–200. doi: 10.1016/j.bios.2018.03.041</mixed-citation><mixed-citation xml:lang="ru">Zhang R., Wei M., Chen S., et al, A cell viability assessment method based on area-normalized impedance spectrum (ANIS) // Biosens Bioelectron. 2018. Vol. 110. P. 193–200. doi: 10.1016/j.bios.2018.03.041</mixed-citation></citation-alternatives></ref><ref id="B69"><label>69.</label><citation-alternatives><mixed-citation xml:lang="en">Bonnier F, Keating ME, Wróbel TP, et al. Cell viability assessment using the Alamar blue assay: a comparison of 2D and 3D cell culture models. Toxicol In Vitro. 2015;29(1):124–131. doi: 10.1016/j.tiv.2014.09.014</mixed-citation><mixed-citation xml:lang="ru">Bonnier F., Keating M.E., Wróbel T.P., et al. Cell viability assessment using the Alamar blue assay: a comparison of 2D and 3D cell culture models // Toxicol In Vitro. 2015. Vol. 29, N 1. P. 124–131. doi: 10.1016/j.tiv.2014.09.014</mixed-citation></citation-alternatives></ref><ref id="B70"><label>70.</label><citation-alternatives><mixed-citation xml:lang="en">Walzl A, Unger C, Kramer N, et al. The resazurin reduction assay can distinguish cytotoxic from cytostatic compounds in spheroid screening assays. J Biomol Screen. 2014;19(7):1047–1059. doi: 10.1177/1087057114532352</mixed-citation><mixed-citation xml:lang="ru">Walzl A., Unger C., Kramer N., et al. The resazurin reduction assay can distinguish cytotoxic from cytostatic compounds in spheroid screening assays // J Biomol Screen. 2014. Vol. 19, N 7. P. 1047–1059. doi: 10.1177/1087057114532352</mixed-citation></citation-alternatives></ref><ref id="B71"><label>71.</label><citation-alternatives><mixed-citation xml:lang="en">Gantenbein-Ritter B, Potier E, Zeiter S, et al. Accuracy of three techniques to determine cell viability in 3D tissues or scaffolds. Tissue Eng Part C Methods. 2008;14(4):353–358. doi: 10.1089/ten.tec.2008.0313</mixed-citation><mixed-citation xml:lang="ru">Gantenbein-Ritter B., Potier E., Zeiter S., et al. Accuracy of three techniques to determine cell viability in 3D tissues or scaffolds // Tissue Eng Part C Methods. 2008. Vol. 14, N 4. P. 353–358. doi: 10.1089/ten.tec.2008.0313</mixed-citation></citation-alternatives></ref><ref id="B72"><label>72.</label><citation-alternatives><mixed-citation xml:lang="en">Sanfilippo S, Canis M, Ouchchane L, et al. Viability assessment of fresh and frozen/thawed isolated human follicles: reliability of two methods (Trypan blue and Calcein AM/ethidium homodimer-1). J Assist Reprod Genet. 2011;28(12):1151–1156. doi: 10.1007/s10815-011-9649-y</mixed-citation><mixed-citation xml:lang="ru">Sanfilippo S., Canis M., Ouchchane L., et al. Viability assessment of fresh and frozen/thawed isolated human follicles: reliability of two methods (Trypan blue and Calcein AM/ethidium homodimer-1) // J Assist Reprod Genet. 2011. Vol. 28, N 12. P. 1151–1156. doi: 10.1007/s10815-011-9649-y</mixed-citation></citation-alternatives></ref><ref id="B73"><label>73.</label><citation-alternatives><mixed-citation xml:lang="en">Dittmar R, Potier E, Van Zandvoort M, Ito K. Assessment of cell viability in three-dimensional scaffolds using cellular auto-fluorescence. Tissue Eng Part C Methods. 2012;18(3):198–204. doi: 10.1089/ten.tec.2011.0334</mixed-citation><mixed-citation xml:lang="ru">Dittmar R., Potier E., Van Zandvoort M., Ito K. Assessment of cell viability in three-dimensional scaffolds using cellular auto-fluorescence // Tissue Eng Part C Methods. 2012. Vol. 18, N 3. P. 198–204. doi: 10.1089/ten.tec.2011.0334</mixed-citation></citation-alternatives></ref><ref id="B74"><label>74.</label><citation-alternatives><mixed-citation xml:lang="en">Kessel S, Cribbes S, Bonasu S, et al. Real-time viability and apoptosis kinetic detection method of 3D multicellular tumor spheroids using the Celigo Image Cytometer. Cytom Part A. 2017;91(9):883–892. doi: 10.1002/cyto.a.23143</mixed-citation><mixed-citation xml:lang="ru">Kessel S., Cribbes S., Bonasu S., et al. Real-time viability and apoptosis kinetic detection method of 3D multicellular tumor spheroids using the Celigo Image Cytometer // Cytom Part A. 2017. Vol. 91, N 9. P. 883–892. doi: 10.1002/cyto.a.23143</mixed-citation></citation-alternatives></ref><ref id="B75"><label>75.</label><citation-alternatives><mixed-citation xml:lang="en">Chabert C, Laporte C, Fertin A, et al. New automatized method of 3D multiculture viability analysis based on confocal imagery: application to islets and mesenchymal stem cells co-encapsulation. Front Endocrinol (Lausanne). 2018;9:272. doi: 10.3389/fendo.2018.00272</mixed-citation><mixed-citation xml:lang="ru">Chabert C., Laporte C., Fertin A., et al. New automatized method of 3D multiculture viability analysis based on confocal imagery: application to islets and mesenchymal stem cells co-encapsulation // Front Endocrinol (Lausanne). 2018. Vol. 9. P. 272. doi: 10.3389/fendo.2018.00272</mixed-citation></citation-alternatives></ref><ref id="B76"><label>76.</label><citation-alternatives><mixed-citation xml:lang="en">Forsythe SD, Devarasetty M, Shupe T, Bishop C. Environmental toxin screening using human-derived 3d bioengineered liver and cardiac organoids. Front Public Heal. 2018;6:1–10. doi: 10.3389/fpubh.2018.00103</mixed-citation><mixed-citation xml:lang="ru">Forsythe S.D., Devarasetty M., Shupe T., Bishop C. Environmental toxin screening using human-derived 3D bioengineered liver and cardiac organoids // Front Public Heal. 2018. Vol. 6. P. 1–10. doi: 10.3389/fpubh.2018.00103</mixed-citation></citation-alternatives></ref><ref id="B77"><label>77.</label><citation-alternatives><mixed-citation xml:lang="en">https://worldwide.promega.com/ [Internet]. 3D Cell Viability Assay. Available from: https://www.promega.co.uk/products/cell-health-assays/cell-viability-and-cytotoxicity-assays/celltiter-glo-3d-cell-viability-assay/?catNum=G9681&amp;gclid=CjwKCAjw6raYBhB7EiwABge5KvC1d1YNEzYbQfDa-H3Uh_Jjlc72nBKIq9QbNN4Jdh3Ap5HO79TG9RoCY1EQAvD_BwE</mixed-citation><mixed-citation xml:lang="ru">https://worldwide.promega.com/ [Internet]. 3D Cell Viability Assay. Доступ по ссылке: https://www.promega.co.uk/products/cell-health-assays/cell-viability-and-cytotoxicity-assays/celltiter-glo-3d-cell-viability-assay/?catNum=G9681&amp;gclid=CjwKCAjw6raYBhB7EiwABge5KvC1d1YNEzYbQfDa-H3Uh_Jjlc72nBKIq9QbNN4Jdh3Ap5HO79TG9RoCY1EQAvD_BwE</mixed-citation></citation-alternatives></ref><ref id="B78"><label>78.</label><citation-alternatives><mixed-citation xml:lang="en">Dominijanni AJ, Devarasetty M, Forsythe SD, et al. Cell viability assays in three-dimensional hydrogels: a comparative study of accuracy. Tissue Eng Part C Methods. 2021;27(7):401–410. doi: 10.1089/ten.tec.2021.0060</mixed-citation><mixed-citation xml:lang="ru">Dominijanni A.J., Devarasetty M., Forsythe S.D., et al. Cell viability assays in three-dimensional hydrogels: a comparative study of accuracy // Tissue Eng Part C Methods. 2021. Vol. 27, N 7. P. 401–410. doi: 10.1089/ten.tec.2021.0060</mixed-citation></citation-alternatives></ref><ref id="B79"><label>79.</label><citation-alternatives><mixed-citation xml:lang="en">Spreda M, Hauptmann N, Lehner V, et al. Porous 3D scaffolds enhance msc vitality and reduce osteoclast activity. Molecules. 2021;26(20):6258. doi: 10.3390/molecules26206258</mixed-citation><mixed-citation xml:lang="ru">Spreda M., Hauptmann N., Lehner V., et al. Porous 3D scaffolds enhance msc vitality and reduce osteoclast activity // Molecules. 2021. Vol. 26, N 20. P. 6258. doi: 10.3390/molecules26206258</mixed-citation></citation-alternatives></ref><ref id="B80"><label>80.</label><citation-alternatives><mixed-citation xml:lang="en">Eremeev AV, Zubkova OA, Ruchko ES, et al. Key parameters of autologous biomedical product for cartilage tissue repair. Medicine of Extreme Situations. 2020;22(4):59–66. doi: 10.47183/mes.2020.014</mixed-citation><mixed-citation xml:lang="ru">Еремеев A.В., Зубкова О.А., Ручко Е.С., и др. Ключевые характеристики аутологичного биомедицинского продукта для коррекции дефекта хрящевой ткани // Медицина экстремальных ситуаций. 2020. Т. 22, № 4. С. 59–66. doi: 10.47183/mes.2020.014</mixed-citation></citation-alternatives></ref></ref-list></back></article>
