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<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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Oncohematology</journal-id><journal-title-group><journal-title xml:lang="en">Oncohematology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкогематология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1818-8346</issn><issn publication-format="electronic">2413-4023</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">71</article-id><article-id pub-id-type="doi">10.17650/1818-8346-2012-7-4-11-15</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>NEW TRENDS IN MEDICAL SCIENCE</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>НОВЫЕ НАПРАВЛЕНИЯ МЕДИЦИНСКОЙ НАУКИ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Fullerene and oxidative stress</article-title><trans-title-group xml:lang="ru"><trans-title>Фуллерены и оксидативный стресс</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Orlova</surname><given-names>M. A.</given-names></name><name xml:lang="ru"><surname>Орлова</surname><given-names>М. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>Химический факультет, кафедра радиохимии</p></bio><email>orlova.radiochem@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Trofimova</surname><given-names>T. P.</given-names></name><name xml:lang="ru"><surname>Трофимова</surname><given-names>Т. П.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>Химический факультет, кафедра радиохимии</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Orlov</surname><given-names>A. P.</given-names></name><name xml:lang="ru"><surname>Орлов</surname><given-names>А. П.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>медико-биологический факультет, кафедра медицинских нанобиотехнологий</p></bio><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Shatalov</surname><given-names>O. A.</given-names></name><name xml:lang="ru"><surname>Шаталов</surname><given-names>О. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>фармацевтический факультет, кафедра фармакологии</p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Svistunov</surname><given-names>A. A.</given-names></name><name xml:lang="ru"><surname>Свистунов</surname><given-names>А. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>фармацевтический факультет, кафедра фармакологии</p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Napolov</surname><given-names>Yu. K.</given-names></name><name xml:lang="ru"><surname>Наполов</surname><given-names>Ю. К.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>фармацевтический факультет, кафедра фармакологии</p></bio><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Chekhonin</surname><given-names>V. P.</given-names></name><name xml:lang="ru"><surname>Чехонин</surname><given-names>В. П.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="ru"><p>медико-биологический факультет, кафедра медицинских нанобиотехнологий</p></bio><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">M.V. Lomonosov Moscow State University</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВПО «Московский государственный университет им. М.В. Ломоносова»</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">N.I. Pirogov Russian National Research Medical University</institution></aff><aff><institution xml:lang="ru">ГБОУ ВПО «Российский научно-исследовательский медицинский университет им. Н.И. Пирогова» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">I.M. Sechenov Moscow State Medical University</institution></aff><aff><institution xml:lang="ru">ГБОУ ВПО «Первый Московский государственный медицинский университет им. И.М. Сеченова» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2012-11-23" publication-format="electronic"><day>23</day><month>11</month><year>2012</year></pub-date><volume>7</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>11</fpage><lpage>15</lpage><history><date date-type="received" iso-8601-date="2014-07-23"><day>23</day><month>07</month><year>2014</year></date><date date-type="accepted" iso-8601-date="2014-07-23"><day>23</day><month>07</month><year>2014</year></date></history><permissions><copyright-year>2012</copyright-year><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncohematology.abvpress.ru/ongm/article/view/71">https://oncohematology.abvpress.ru/ongm/article/view/71</self-uri><abstract xml:lang="en"><p>Fullerene derivatives superfamily attracts a serious attention as antiviral and anticancer agents and drug delivery carriers as well. A large number of such fullerene С60 derivatives obtained to date. However, there is an obvious deficit of information about causes and mechanisms of immediately and long-term consequences of their effects in vivo which is a true obstacle on the way leading to their practical medical using. First, this concerns their impact on the proliferation, apoptosis and necrosis regulation. Fullerene nanoparticle functionalization type, their sizes and surface nanopathology are of great importance for further promoting of either cytoprotective or cytotoxic effects. One of the main effects of fullerenes on living systems is the reactive oxygen species (ROS) formation induction. This lecture provides a modern concept analysis regarding fullerenes effects on ROS formation and modulation of proliferation and apoptosis in normal and tumor cells.</p></abstract><trans-abstract xml:lang="ru"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>fullerenes</kwd><kwd>apoptosis</kwd><kwd>oxidative stress</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>фуллерены</kwd><kwd>апоптоз</kwd><kwd>оксидативный стресс.</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Orlova M.A., Orlov A.P. Role of zinc in an organism and its influence on processes leading to apoptosis. Br J Med Res 2011;1:239–305.</mixed-citation><mixed-citation xml:lang="ru">Orlova M.A., Orlov A.P. Role of zinc in an organism and its influence on processes leading to apoptosis. Br J Med Res 2011;1:239–305.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Portt L., Norman G., Clapp C., Greenwood M. Anti-apoptosis and cell survival. Biochim Biophys Acta 2011;1813:238–59.</mixed-citation><mixed-citation xml:lang="ru">Portt L., Norman G., Clapp C., Greenwood M. Anti-apoptosis and cell survival. Biochim Biophys Acta 2011;1813:238–59.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Shvedova A.A., Kagan V.E., Fadeel B. Close encounters of the small kind: adverse effects of man-made materials interfacing with the nano-cosmos of biological systems. Annu Rev Pharmacol Toxicol 2010;50:63–88.</mixed-citation><mixed-citation xml:lang="ru">Shvedova A.A., Kagan V.E., Fadeel B. Close encounters of the small kind: adverse effects of man-made materials interfacing with the nano-cosmos of biological systems. Annu Rev Pharmacol Toxicol 2010;50:63–88.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Markovic Z., Trajkovic V. Biomedical potential of the reactive oxygen species generation and quenching by fullerenes (C60). Biomaterials 2008;29:3561–73.</mixed-citation><mixed-citation xml:lang="ru">Markovic Z., Trajkovic V. Biomedical potential of the reactive oxygen species generation and quenching by fullerenes (C60). Biomaterials 2008;29:3561–73.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Yamakoshi Y., Umezawa N., Ryu A. et al. Active oxygen species generated from photoexcited fullerene (C60) as potential medicines: O2-* versus 1O2. J Am Chem Soc 2003;125:12803–9.</mixed-citation><mixed-citation xml:lang="ru">Yamakoshi Y., Umezawa N., Ryu A. et al. Active oxygen species generated from photoexcited fullerene (C60) as potential medicines: O2-* versus 1O2. J Am Chem Soc 2003;125:12803–9.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Sayes C.M., Gobin A.M., Ausman K.D. et al. Nano- C60 cytotoxicity is due to lipid peroxidation. Biomaterials 2005;26:7587–95.</mixed-citation><mixed-citation xml:lang="ru">Sayes C.M., Gobin A.M., Ausman K.D. et al. Nano- C60 cytotoxicity is due to lipid peroxidation. Biomaterials 2005;26:7587–95.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Scrivens W.A., Tour J.M., Creek K.E., Pirisi L. Synthesis of 14C-labeled C60, its suspension in water, and its uptake by human keratinocytes. J Am Chem Soc 1994;116:4517–8.</mixed-citation><mixed-citation xml:lang="ru">Scrivens W.A., Tour J.M., Creek K.E., Pirisi L. Synthesis of 14C-labeled C60, its suspension in water, and its uptake by human keratinocytes. J Am Chem Soc 1994;116:4517–8.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Maeda R., Noiri E., Isobe H. et al. A water-soluble fullerene vesicle alleviates angiotensin II-induced oxidative stress in human umbilical venous endothelial cells. Hypertension Res 2008;31:141–51.</mixed-citation><mixed-citation xml:lang="ru">Maeda R., Noiri E., Isobe H. et al. A water-soluble fullerene vesicle alleviates angiotensin II-induced oxidative stress in human umbilical venous endothelial cells. Hypertension Res 2008;31:141–51.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Kolosnjaj J., Szwarc H., Moussa F. Toxicity studies of fullerenes and derivatives. Adv Exp Med Biol 2007;620:168–80.</mixed-citation><mixed-citation xml:lang="ru">Kolosnjaj J., Szwarc H., Moussa F. Toxicity studies of fullerenes and derivatives. Adv Exp Med Biol 2007;620:168–80.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Jia G., Wang H., Yan L. et al. Cytotoxicity of carbon nanomaterials: singlewall nanotube, multi-wall nanotube, and fullerene. Environ Sci Technol 2005;39:1378–83.</mixed-citation><mixed-citation xml:lang="ru">Jia G., Wang H., Yan L. et al. Cytotoxicity of carbon nanomaterials: singlewall nanotube, multi-wall nanotube, and fullerene. Environ Sci Technol 2005;39:1378–83.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Sayes C.M., Marchione A.A., Reed K.L., Warheit D.B. Comparative pulmonary toxicity assessments of C60 water suspensions in rats: few differences in fullerene toxicity in vivo in contrast to in vitro profiles. Nano Lett 2007;7:2399–406.</mixed-citation><mixed-citation xml:lang="ru">Sayes C.M., Marchione A.A., Reed K.L., Warheit D.B. Comparative pulmonary toxicity assessments of C60 water suspensions in rats: few differences in fullerene toxicity in vivo in contrast to in vitro profiles. Nano Lett 2007;7:2399–406.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Baker G.L., Gupta A., Clark M.L. et al. Inhalation toxicity and lung toxicokinetics of C60 fullerene nanoparticles and microparticles. Toxicol Sci 2008;101:122–31.</mixed-citation><mixed-citation xml:lang="ru">Baker G.L., Gupta A., Clark M.L. et al. Inhalation toxicity and lung toxicokinetics of C60 fullerene nanoparticles and microparticles. Toxicol Sci 2008;101:122–31.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Horie M., Nishio K., Kato H. et al. In vitro evaluation of cellular responses induced by stable fullerene C60 medium dispersion. J Biochem 2010;148:289–98.</mixed-citation><mixed-citation xml:lang="ru">Horie M., Nishio K., Kato H. et al. In vitro evaluation of cellular responses induced by stable fullerene C60 medium dispersion. J Biochem 2010;148:289–98.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Zhou S., Burger C., Chu B. et al. Spherical bilayer vesicles of fullerene-based surfactants in water: a laser light scattering study. Science 2001;291:1944–7.</mixed-citation><mixed-citation xml:lang="ru">Zhou S., Burger C., Chu B. et al. Spherical bilayer vesicles of fullerene-based surfactants in water: a laser light scattering study. Science 2001;291:1944–7.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Sawamura M., Kawai K., Matsuo Y. et al. Stacking of conical mesogens with a fullerene apex into polar columns in crystals and liquid crystals. Nature 2002;419:702–5.</mixed-citation><mixed-citation xml:lang="ru">Sawamura M., Kawai K., Matsuo Y. et al. Stacking of conical mesogens with a fullerene apex into polar columns in crystals and liquid crystals. Nature 2002;419:702–5.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Yin J.J., Lao F., Fu P.P. et al. The scavenging of reactive oxygen species and the potential for cell protection by functionalized fullerene materials. Biomaterials 2009;30:611–21.</mixed-citation><mixed-citation xml:lang="ru">Yin J.J., Lao F., Fu P.P. et al. The scavenging of reactive oxygen species and the potential for cell protection by functionalized fullerene materials. Biomaterials 2009;30:611–21.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Husebo L.O., Sitharaman B., Furukawa K. et al. Fullerenols revisited as stable radical anions. J Am Chem Soc 2004;126:12055–64.</mixed-citation><mixed-citation xml:lang="ru">Husebo L.O., Sitharaman B., Furukawa K. et al. Fullerenols revisited as stable radical anions. J Am Chem Soc 2004;126:12055–64.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Yamakoshi Y.N., Yagami T., Sueyoshi S., Miyata N. Acridine adduct of [60]fullerene with enhanced DNA-cleaving activity. J Org Chem 1996;61:7236–7.</mixed-citation><mixed-citation xml:lang="ru">Yamakoshi Y.N., Yagami T., Sueyoshi S., Miyata N. Acridine adduct of [60]fullerene with enhanced DNA-cleaving activity. J Org Chem 1996;61:7236–7.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Makha M., Purich A., Raston C.L., Sobolev A.N. Structural diversity of hostguest and intercalation complexes of fullerene C60. Eur J Inorg Chem 2006;3:507–17.</mixed-citation><mixed-citation xml:lang="ru">Makha M., Purich A., Raston C.L., Sobolev A.N. Structural diversity of hostguest and intercalation complexes of fullerene C60. Eur J Inorg Chem 2006;3:507–17.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Deguchi S., Mukai S.A., Tsudome M., Horikoshi K. Facile generation of fullerene nanoparticles by hand-grinding. Adv Mater 2006;18:729–32.</mixed-citation><mixed-citation xml:lang="ru">Deguchi S., Mukai S.A., Tsudome M., Horikoshi K. Facile generation of fullerene nanoparticles by hand-grinding. Adv Mater 2006;18:729–32.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Quaranta A., Zhang Y., Filippone S. et al. Photophysical studies of six amphiphilic 2:1 cyclodextrin:[60]fullerene derivatives. Chem Phys 2006;325:397–403.</mixed-citation><mixed-citation xml:lang="ru">Quaranta A., Zhang Y., Filippone S. et al. Photophysical studies of six amphiphilic 2:1 cyclodextrin:[60]fullerene derivatives. Chem Phys 2006;325:397–403.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Dhawan A., Taurozzi J.S., Pandey A.K. et al. Stable colloidal dispersions of C60 fullerenes in water: evidence for genotoxicity. Environ Sci Technol 2006;40:7394–401.</mixed-citation><mixed-citation xml:lang="ru">Dhawan A., Taurozzi J.S., Pandey A.K. et al. Stable colloidal dispersions of C60 fullerenes in water: evidence for genotoxicity. Environ Sci Technol 2006;40:7394–401.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Deguchi S., Alargova R.G., Tsujii K. table dispersions of fullerenes, C60 and C70, in water: preparation and characterization. Langmuir 2001;17:6013–7.</mixed-citation><mixed-citation xml:lang="ru">Deguchi S., Alargova R.G., Tsujii K. table dispersions of fullerenes, C60 and C70, in water: preparation and characterization. Langmuir 2001;17:6013–7.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Lyon D.Y., Adams L.K., Falkner J.C., Alvarez P.J. Antibacterial activity of fullerene water suspensions: effects of preparation method and particle size. Environ Sci Technol 2006;40:4360–6.</mixed-citation><mixed-citation xml:lang="ru">Lyon D.Y., Adams L.K., Falkner J.C., Alvarez P.J. Antibacterial activity of fullerene water suspensions: effects of preparation method and particle size. Environ Sci Technol 2006;40:4360–6.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Brant J.A., Labille J., Bottero J.Y., Wiesner M.R. Characterizing the impact of preparation method on fullerene cluster structure and chemistry. Langmuir 2006;22:3878–85.</mixed-citation><mixed-citation xml:lang="ru">Brant J.A., Labille J., Bottero J.Y., Wiesner M.R. Characterizing the impact of preparation method on fullerene cluster structure and chemistry. Langmuir 2006;22:3878–85.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Cook S.M., Aker W.G., Rasulev B.F. et al.Choosing safe dispersing media for С60 fullerenes by using cytotoxicity tests on the bacterium Escherichia coli. J Hazar Mater 2010;176:367–73.</mixed-citation><mixed-citation xml:lang="ru">Cook S.M., Aker W.G., Rasulev B.F. et al.Choosing safe dispersing media for С60 fullerenes by using cytotoxicity tests on the bacterium Escherichia coli. J Hazar Mater 2010;176:367–73.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Cho M., Fortner J.D., Hughes J.B., Kim J.H. Escherichia coli inactivation by water-soluble, ozonated С60 derivative: kinetics and mechanisms. Envir Sci Technol 2009;43:7410–5.</mixed-citation><mixed-citation xml:lang="ru">Cho M., Fortner J.D., Hughes J.B., Kim J.H. Escherichia coli inactivation by water-soluble, ozonated С60 derivative: kinetics and mechanisms. Envir Sci Technol 2009;43:7410–5.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Каркищенко Н.Н. Нанобезопасность: новые подходы к оценке рисков и токсичности наноматериалов. Биомедицина 2009;1:5–27.</mixed-citation><mixed-citation xml:lang="ru">Каркищенко Н.Н. Нанобезопасность: новые подходы к оценке рисков и токсичности наноматериалов. Биомедицина 2009;1:5–27.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Nishimura T., Kubota R., Tahara M. et al. Biological effects of fullerene С60 in mouse embryonic stem cells. Toxicol Lett 2006;164S:S214.</mixed-citation><mixed-citation xml:lang="ru">Nishimura T., Kubota R., Tahara M. et al. Biological effects of fullerene С60 in mouse embryonic stem cells. Toxicol Lett 2006;164S:S214.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Trpkovic A., Todorovic-Markovic B., Kleut D. et al. Oxidative stress-mediated hemolytic activity of solvent exchangeprepared fullerene (С60) nanoparticles. Nanotechnol 2010;21(37):375102.</mixed-citation><mixed-citation xml:lang="ru">Trpkovic A., Todorovic-Markovic B., Kleut D. et al. Oxidative stress-mediated hemolytic activity of solvent exchangeprepared fullerene (С60) nanoparticles. Nanotechnol 2010;21(37):375102.</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Costa C.L.A., Chaves I.S., Ventura-Lima J. et al. In vitro evaluation of co-exposure of arsenium and an organic nanomaterial (fullerene, С60) in zebrafish hepatocytes. Comp Biochem Physiol C 2012;155:206–12.</mixed-citation><mixed-citation xml:lang="ru">Costa C.L.A., Chaves I.S., Ventura-Lima J. et al. In vitro evaluation of co-exposure of arsenium and an organic nanomaterial (fullerene, С60) in zebrafish hepatocytes. Comp Biochem Physiol C 2012;155:206–12.</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. Hu Z., Guan W., Wang W. et al. Protective effects of a novel cystine С60 derivative on hydrogen peroxide-induced apoptosis in rat pheochromocytoma PC12 cells. Chem Biol Interact 2007;167:135–44.</mixed-citation><mixed-citation xml:lang="ru">Hu Z., Guan W., Wang W. et al. Protective effects of a novel cystine С60 derivative on hydrogen peroxide-induced apoptosis in rat pheochromocytoma PC12 cells. Chem Biol Interact 2007;167:135–44.</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33. Hu Z., Guan W., Wang W. et al. Synthesis of amphiphilic amino acid С60 derivatives and their protective effect on hydrogen peroxide-induced apoptosis in rat pheochromocytoma cells. Carbon 2008;46:99–109.</mixed-citation><mixed-citation xml:lang="ru">Hu Z., Guan W., Wang W. et al. Synthesis of amphiphilic amino acid С60 derivatives and their protective effect on hydrogen peroxide-induced apoptosis in rat pheochromocytoma cells. Carbon 2008;46:99–109.</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34. Wang I.C., Tai L.A., Lee D.D. et al. С60 and water-soluble fullerene derivatives as antioxidants against radical-initiated lipid peroxidation. J Med Chem 1999;42: 4614–20.</mixed-citation><mixed-citation xml:lang="ru">Wang I.C., Tai L.A., Lee D.D. et al. С60 and water-soluble fullerene derivatives as antioxidants against radical-initiated lipid peroxidation. J Med Chem 1999;42: 4614–20.</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35. Monti D., Moretti L., Salvioli S. et al. С60 carboxyfullerene exerts a protective activity against oxidative stress-induced apoptosis in human peripheral bloodmononuclear cells. Biochem Biophys Res Commun 2000;277:711–7.</mixed-citation><mixed-citation xml:lang="ru">Monti D., Moretti L., Salvioli S. et al. С60 carboxyfullerene exerts a protective activity against oxidative stress-induced apoptosis in human peripheral bloodmononuclear cells. Biochem Biophys Res Commun 2000;277:711–7.</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">36. Guan S., Bao Y., Jiang B., An L. Protective effect of protocatechuic acid from Alpinia oxyphyllaon hydrogen peroxideinduced oxidative PC12 cell death. Eur J Pharmacol 2006;538:73–9.</mixed-citation><mixed-citation xml:lang="ru">Guan S., Bao Y., Jiang B., An L. Protective effect of protocatechuic acid from Alpinia oxyphyllaon hydrogen peroxideinduced oxidative PC12 cell death. Eur J Pharmacol 2006;538:73–9.</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">37. Xiao L., Takada H., Maeda K. et al. Antioxidant effects of water-soluble fullerene derivatives against ultraviolet ray or peroxylipid through their action of scavenging the reactive oxygen species in human skin keratinocytes. Biomed Pharmacotherapy 2005;59:351–8.</mixed-citation><mixed-citation xml:lang="ru">Xiao L., Takada H., Maeda K. et al. Antioxidant effects of water-soluble fullerene derivatives against ultraviolet ray or peroxylipid through their action of scavenging the reactive oxygen species in human skin keratinocytes. Biomed Pharmacotherapy 2005;59:351–8.</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">38. Alcaraz M.J., Megías J., García-Arnandis I. et al. New molecular targets for the treatment of osteoarthritis. iochem Pharmacol 2010;80:13–21.</mixed-citation><mixed-citation xml:lang="ru">Alcaraz M.J., Megías J., García-Arnandis I. et al. New molecular targets for the treatment of osteoarthritis. iochem Pharmacol 2010;80:13–21.</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">39. Bal R., Turk G., Tuzcu M. et al. Protective effects of nanostructures of hydrated С60 fullerene on reproductive function in streptozotocin-diabetic male rats. Toxicology 2011;282:69–81.</mixed-citation><mixed-citation xml:lang="ru">Bal R., Turk G., Tuzcu M. et al. Protective effects of nanostructures of hydrated С60 fullerene on reproductive function in streptozotocin-diabetic male rats. Toxicology 2011;282:69–81.</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">40. Mirkov S.M., Djordjevic A.N., Andric N.L. et al. Nitric oxide-scavenging activity of polyhydroxylated fullerenol, С60(OH)24. Nitric Oxide 2004;11:201–7.</mixed-citation><mixed-citation xml:lang="ru">Mirkov S.M., Djordjevic A.N., Andric N.L. et al. Nitric oxide-scavenging activity of polyhydroxylated fullerenol, С60(OH)24. Nitric Oxide 2004;11:201–7.</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">41. Bogdanovic G., Koji V., Dordevic A. t al. Modulating activity of fullerol С60(OH)22 on doxorubicin-induced cytotoxicity. Toxicol In Vitro 2004;18: 629–37.</mixed-citation><mixed-citation xml:lang="ru">Bogdanovic G., Koji V., Dordevic A. t al. Modulating activity of fullerol С60(OH)22 on doxorubicin-induced cytotoxicity. Toxicol In Vitro 2004;18: 629–37.</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">42. Wielgus A.R., Zhao B., Chignell C.F. et al. Phototoxicity and cytotoxicity of fullerol in human retinal pigment epithelial cells. Toxicol Appl Pharmacol 2010; 242:79–90.</mixed-citation><mixed-citation xml:lang="ru">Wielgus A.R., Zhao B., Chignell C.F. et al. Phototoxicity and cytotoxicity of fullerol in human retinal pigment epithelial cells. Toxicol Appl Pharmacol 2010; 242:79–90.</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">43. Cagle D.W., Kennel S.J., Mirzadeh S. et al. In vivo studies of fullerene-based materials using endohedral metallofullerene radiotracers. Proc Natl Acad Sci USA 1999;96:5182–7.</mixed-citation><mixed-citation xml:lang="ru">Cagle D.W., Kennel S.J., Mirzadeh S. et al. In vivo studies of fullerene-based materials using endohedral metallofullerene radiotracers. Proc Natl Acad Sci USA 1999;96:5182–7.</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">44. Oberdorster E. Manufactured nanomaterials (fullerenes, C60) induce oxidative stress in the brain of juvenile largemouth bass. Environ Health Perspect 2004;112:1058–62.</mixed-citation><mixed-citation xml:lang="ru">Oberdorster E. Manufactured nanomaterials (fullerenes, C60) induce oxidative stress in the brain of juvenile largemouth bass. Environ Health Perspect 2004;112:1058–62.</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">45. Lao F., Chen L., Li W. et al. Fullerene nanoparticles selectively enter oxidationdamaged cerebral microvessel endothelial cells and inhibit JNK related apoptosis. Acs Nano 2009;3:3358–68.</mixed-citation><mixed-citation xml:lang="ru">Lao F., Chen L., Li W. et al. Fullerene nanoparticles selectively enter oxidationdamaged cerebral microvessel endothelial cells and inhibit JNK related apoptosis. Acs Nano 2009;3:3358–68.</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">46. Lin J., Wu C. Surface characterization and platelet adhesion studies on polyurethane surface immobilized with C60. Biomaterials 1999;20:1613–20.</mixed-citation><mixed-citation xml:lang="ru">Lin J., Wu C. Surface characterization and platelet adhesion studies on polyurethane surface immobilized with C60. Biomaterials 1999;20:1613–20.</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">47. Linazasoro G. Potential applications of nanotechnologies to Parkinson’s disease therapy. Parkinson Relat Disor 2008; 14:383–92.</mixed-citation><mixed-citation xml:lang="ru">Linazasoro G. Potential applications of nanotechnologies to Parkinson’s disease therapy. Parkinson Relat Disor 2008; 14:383–92.</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">48. Morimoto Y., Hirohashi M., Ogami A. et al. Inflammogenic effect of wellcharacterized fullerenes in inhalation and ntratracheal instillation studies. Part Fibre Toxicol 2010;7:4–22.</mixed-citation><mixed-citation xml:lang="ru">Morimoto Y., Hirohashi M., Ogami A. et al. Inflammogenic effect of wellcharacterized fullerenes in inhalation and ntratracheal instillation studies. Part Fibre Toxicol 2010;7:4–22.</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">49. Lee Y.T., Chiang L.Y., Chen W.J., Hsu H.C. Water-soluble hexasulfobutyl-[60]-fullerene inhibits low-density lipoprotein oxidation in aqueous and lipophilic phases. Proc Soc Exp Biol Med 2000;224:69–75.</mixed-citation><mixed-citation xml:lang="ru">Lee Y.T., Chiang L.Y., Chen W.J., Hsu H.C. Water-soluble hexasulfobutyl-[60]-fullerene inhibits low-density lipoprotein oxidation in aqueous and lipophilic phases. Proc Soc Exp Biol Med 2000;224:69–75.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
