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Safonova T.N.

Krasnov Research Institute of Eye Diseases

Novikov I.A.

Krasnov Research Institute of Eye Diseases;
Prokhorov General Physics Institute of the Russian Academy of Sciences

Zaitseva G.V.

Krasnov Research Institute of Eye Diseases

Dobretsova E.A.

Prokhorov General Physics Institute of the Russian Academy of Sciences

Solodovnikov V.I.

Center of Information Technologies in Design of the Russian Academy of Sciences

Possibilities of optical fluorescence spectral decomposition of meibum

Authors:

Safonova T.N., Novikov I.A., Zaitseva G.V., Dobretsova E.A., Solodovnikov V.I.

More about the authors

Journal: Russian Annals of Ophthalmology. 2025;141(5): 29‑36

Read: 711 times


To cite this article:

Safonova TN, Novikov IA, Zaitseva GV, Dobretsova EA, Solodovnikov VI. Possibilities of optical fluorescence spectral decomposition of meibum. Russian Annals of Ophthalmology. 2025;141(5):29‑36. (In Russ.)
https://doi.org/10.17116/oftalma202514105129

References:

  1. Butovich IA. Tear film lipids. Experimental Eye Research. 2013;117:4-27.  https://doi.org/10.1016/j.exer.2013.05.010
  2. Traipe F, Traipe L, Salinas-Toro D, López D, Valenzuela F, Pérez C, Cartes C, Zuazo F, Varela P, Toledo-Araya H, López-Solís R. Zone I of Tear Microdesiccates Is a Lipid-Containing Structure. Cornea. 2017;36(2):229-235.  https://doi.org/10.1097/ICO.0000000000001070
  3. Maki KL, Braun RJ, Barron GA. The influence of a lipid reservoir on the tear film formation. Mathematical Medicine and Biology. 2020;37(2):363-388.  https://doi.org/10.1093/imammb/dqz018
  4. Butovich IA, Wilkerson A, Yuksel S. Dysregulation of Lipid Metabolism in Aging Meibomian Glands and Its Molecular Markers. International Journal of Molecular Sciences. 2023;24(17):13512. https://doi.org/10.3390/ijms241713512
  5. Butovich IA, Lu H, McMahon A, Ketelson H, Senchyna M, Meadows D, Campbell E, Molai M, Linsenbardt E. Biophysical and morphological evaluation of human normal and dry eye meibum using hot stage polarized light microscopy. Investigative Ophthalmology & Visual Science. 2014;55:87-101.  https://doi.org/10.1167/iovs.13-13355
  6. Tsai PS, Evans JE, Green KM, Sullivan RM, Schaumberg DA, Richards SM, Dana MR, Sullivan DA. Proteomic analysis of human meibomian gland secretions. British Journal of Ophthalmology. 2006;90(3):372-377.  https://doi.org/10.1136/bjo.2005.080846
  7. Jeyalatha MV, Qu Y, Liu Z, Ou S, He X, Bu J, Li S, Reinach PS, Liu Z, Li W. Function of meibomian gland: Contribution of proteins. Experimental Eye Research. 2017;163:29-36.  https://doi.org/10.1016/j.exer.2017.06.009
  8. Qi X, Ren SW, Zhang F, Wang YQ. The involvement of proline-rich protein Mus musculus predicted gene 4736 in ocular surface functions. International Journal of Ophthalmology. 2016;9(8):1121-1126. https://doi.org/10.18240/ijo.2016.08.06
  9. Pattamatta U, Willcox M, Stapleton F, Garrett Q. Bovine lactoferrin promotes corneal wound healing and suppresses IL-1 expression in alkali wounded mouse cornea. Current Eye Research. 2013;38(11):1110-1117. https://doi.org/10.3109/02713683.2013.811259
  10. Butovich IA, Suzuki T. Effects of Aging on Human Meibum. Investigative Ophthalmology & Visual Science. 2021;62(12):23.  https://doi.org/10.1167/iovs.62.12.23
  11. Tong L, Zhou L, Beuerman RW, Zhao SZ, Li XR. Association of tear proteins with Meibomian gland disease and dry eye symptoms. Br J Ophthalmol. 2011 Jun;95(6):848-52.  https://doi.org/10.1136/bjo.2010.185256
  12. Saaren-Seppälä H, Jauhiainen M, Tervo TM, Redl B, Kinnunen PK, Holopainen JM. Interaction of purified tear lipocalin with lipid membranes. Investigative Ophthalmology & Visual Science. 2005;46(10):3649-3656. https://doi.org/10.1167/iovs.05-0176
  13. Gasymov OK, Abduragimov AR, Prasher P, Yusifov TN, Glasgow BJ. Tear lipocalin: evidence for a scavenging function to remove lipids from the human corneal surface. Investigative Ophthalmology & Visual Science. 2005; 46(10):3589-3596. https://doi.org/10.1167/iovs.05-0569
  14. Stopkova R, Hladovcov D, Kokavec J, Vyoral D, Stopka P. Multiple roles of secretory lipocalins (Mup, Obp) in mice. Folia Zoologica. 2009;58(1):29e40.
  15. Regueiro U, López-López M, Varela-Fernández R, Otero-Espinar FJ, Lema I. Biomedical Applications of Lactoferrin on the Ocular Surface. Pharmaceutics. 2023;15(3):865.  https://doi.org/10.3390/pharmaceutics15030865
  16. Pedersen AM, Nauntofte B. Primary Sjögren’s syndrome: Oral aspects on pathogenesis, diagnostic criteria, clinical features and approaches for therapy. Expert Opinion on Pharmacotherapy. 2001;9:1415-1436. https://doi.org/10.1517/14656566.2.9.1415
  17. Flanagan JL, Willcox MD. Role of lactoferrin in the tear film. Biochimie. 2009;91(1):35-43.  https://doi.org/10.1016/j.biochi.2008.07.007
  18. Safonova TN, Zaitseva GV, Burdennyy AM. Polymorphic markers of certain genes in the development of dry keratoconjunctivitis in patients with rheumatoid arthritis and Sjogren’s syndrome. Russian Annals of Ophthalmology. 2019;135(5):254-259. (In Russ.). https://doi.org/10.17116/oftalma2019135052254
  19. Butovich IA. Meibomian glands, meibum, and meibogenesis. Experimental Eye Research. 2017;163:2-16.  https://doi.org/10.1016/j.exer.2017.06.020
  20. Paul AJ, Bickel F, Röhm M, Hospach L, Halder B, Rettich N, Handrick R, Herold EM, Kiefer H, Hesse F. High-throughput analysis of sub-visible mAb aggregate particles using automated fluorescence microscopy imaging. Analytical and Bioanalytical Chemistry. 2017;409(17):4149-4156. https://doi.org/10.1007/s00216-017-0362-2
  21. Patent RF na izobretenie №2362489/2009. Byull. №21. Novikov IA, Kozlov OK, Likhvantseva VG, Osipova EA. Sposob opredeleniya otnositel’nogo soderzhaniya protoporfirina-IX v biologicheskoj tkani. (In Russ.).
  22. Glasgow BJ, Abduragimov AR. Interaction of Ceramides and Tear Lipocalin. Biochimica et Biophysica Acta — Molecular and Cell Biology of Lipids. 2018;1863(4):399-408.  https://doi.org/10.1016/j.bbalip.2018.01.004
  23. Butovich IA, Uchiyama E, McCulley JP. Lipids of human meibum: mass-spectrometric analysis and structural elucidation. Journal of lipid research. 2007;48(10):2220-2235. https://doi.org/10.1194/jlr.M700237-JLR200
  24. Olżyńska A, Wizert A, Štefl M, Iskander DR, Cwiklik L. Mixed polar-nonpolar lipid films as minimalistic models of Tear Film Lipid Layer: A Langmuir trough and fluorescence microscopy study. Biochimica et Biophysica Acta — Biomembranes. 2020;1862(9):183300. https://doi.org/10.1016/j.bbamem.2020.183300
  25. Sato EA, Matsumoto Y, Dogru M, Kaido M, Wakamatsu T, Ibrahim OM, Obata H, Tsubota K. Lacrimal gland in Sjögren’s syndrome. Ophthalmology. 2010;117(5):1055-e3.  https://doi.org/10.1016/j.ophtha.2009.11.034
  26. Versura P, Nanni P, Bavelloni A, Blalock WL, Piazzi M, Roda A, Campos EC. Tear proteomics in evaporative dry eye disease. Eye. 2010;24:1396-1402. https://doi.org/10.1038/eye.2010.7
  27. Saaren-Seppälä H, Jauhiainen M, Tervo TM, Redl B, Kinnunen PK, Holopainen JM. Interaction of purified tear lipocalin with lipid membranes. Investigative Ophthalmology & Visual Science. 2005;46(10):3649-3656. https://doi.org/10.1167/iovs.05-0176
  28. Müller F. Flavin radicals: chemistry and biochemistry. Free Radical Biology and Medicine. 1987;3(3):215-230.  https://doi.org/10.1016/0891-5849(87)90009-8
  29. Lienhart WD, Gudipati V, Macheroux P. The human flavoproteome. Archives of Biochemistry and Biophysics. 2013;535(2):150-162.  https://doi.org/10.1016/j.abb.2013.02.015
  30. Ragan CI, Garland PB. Spectroscopic studies of flavoproteins and non-haem iron proteins of submitochondrial particles of Torulopsis utilis modified by  iron- and sulphate-limited growth in continuous culture. Biochemical Journal. 1971;124(1):171-187.  https://doi.org/10.1042/bj1240171
  31. Safonova TN, Zajceva GV, Timoshenkova EI. Chemical analysis of meibum composition on the background of type 2 diabetes mellitus. Ophthalmological Bulletin. 2024;17(1):89-102. (In Russ.). https://doi.org/10.17816/OV488056
  32. Johnson TV, DeKorver NW, Levasseur VA, Osborne A, Tassoni A, Lorber B, Heller JP, Villasmil R, Bull ND, Martin KR, Tomarev SI. Identification of retinal ganglion cell neuroprotection conferred by platelet-derived growth factor through analysis of the mesenchymal stem cell secretome. Brain. 2014;137(2):503-519.  https://doi.org/10.1093/brain/awt292

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