ИССЛЕДОВАНИЕ РАСПРЕДЕЛЕНИЯ ХЛОРИНОВЫХ ФОТОСЕНСИБИЛИЗАТОРОВ В ДВУХМЕРНЫХ И ТРЕХМЕРНЫХ КЛЕТОЧНЫХ КУЛЬТУРАХ
https://doi.org/10.24931/2413-9432-2017-6-2-4-11
Аннотация
Об авторах
Д. С. Фаррахова
Национальный исследовательский ядерный университет МИФИ; Институт общей физики им. А.М. Прохорова РАН
Россия
Россия
Москва
М. В. Яковец
Белорусский государственный университет; Centre de Recherche en Automatique de Nancy, Université de Lorraine; Institut de Cancérologie de Lorraine
Беларусь
Беларусь
Минск, Nancy, Vandoeuvre-lès-Nancy
В. Б. Лощенов
Национальный исследовательский ядерный университет МИФИ; Институт общей физики им. А.М. Прохорова РАН
Россия
Россия
Москва
L. N. Bolotine
Centre de Recherche en Automatique de Nancy, Université de Lorraine; Institut de Cancérologie de Lorraine
Россия
Россия
Nancy, Vandoeuvre-lès-Nancy
В. П. Зорин
Белорусский государственный университет; Международный государственный экологический институт им. А.Д. Сахарова Белорусского государственного университета
Беларусь
Беларусь
Минск
Список литературы
1. Baker A., Kanofsky J.R. Quenching of singlet oxygen by biomolecules from L1210 leukemia cells // Photochem. Photobiol. – 1992. – Vol. 55, No. 4. – P. 523-528.
2. Moan J. On the diffusion length of singlet oxygen in cells and tissues // J. Photochem. Photobiol. B. – 1990. – Vol. 6, No. 3. – P. 343-344.
3. Shliakhtsin S.V., Trukhachova T.V., Isakau H.A., Istomin Y.P. Pharmacokinetics and biodistribution of Photolon (Fotolon) in intact and tumor-bearing rats // Photodiagnosis Photodyn. Ther. – 2009. – Vol. 6, No. 2. – P. 97-104.
4. Kochneva E.V., Filonenko E.V., Vakulovskaya E.G., et al. Photosensitizer Radachlorin: Skin cancer PDT phase II clinical trials // Photodiagnosis Photodyn. Ther. – 2010. – Vol. 7, No. 4. – P. 258-267.
5. Zorina T.E., Yankovskii I.V., Kravchenko I.E., et al. Liposomal formulations of chlorin e6 ester derivatives and features of their cellular uptake // BSU Her. – 2013. – No. 3. – P. 30-35.
6. Zorin V.P., Michalovsky I.S., Zorina T.E., Khludeyev I.I. Distribution of chlorin-e6 derivatives in biological systems: investigation of pH-effect // Proceeding SPIE. – 1996. – Vol. 2625. – P. 146-155.
7. Соколов С.Н., Федорук С.Л., Трухачева Т.В., Хейдоров В.П. 13{1},15{2}-диметиловый эфир хлорина E6 – новый фотосенсибилизатор. Доказательство структуры и чистоты // Вестник Фармации. – 2016. – № 4 (74). – C. 53-61.
8. Zorin V.P., Khludeyev I.I, Mikhalovsky I.S., et al. Kinetic characteristics of porphyrin distribution in the blood // Proceeding SPIE. – 2000. – Vol. 4059. – P. 139-146.
9. Savitsky V.P., Zorin V.P., Potapnev M.P. Selective phototoxicity of chlorin-e6 derivatives toward leukemic cells // Exp. Oncol. – 2002. – Vol. 24, No. 2. – P. 142-144.
10. Khanna S., Bhatt A.N., Dwarakanath B.S. Chapter 11 – Multicellular Spheroid: 3-D Tissue Culture Model for Cancer Research A2 – Verma, Ashish S. // Animal Biotechnology / ed. Singh A. – San Diego: Academic Press, 2014. – P. 195-210.
11. Patel N.R., Aryasomayajula B., Abouzeid A.H., Torchilin V.P. Cancer cell spheroids for screening of chemotherapeutics and drugdelivery systems // Ther. Deliv. – 2015. – Vol. 6, No. 4. – P. 509-520.
12. Losev A.P., Nichiporovich I.N., Zhuravkin I.N, Zhavrid E.I. Energetics of chlorins as potent photosensitizers of PDT // Proceeding SPIE. – 1996. – Vol. 2924. – P. 40-48.
13. Mojzisova H., Bonneau S., Vever-Bizet C., Brault D. Cellular uptake and subcellular distribution of chlorin e6 as functions of pH and interactions with membranes and lipoproteins // Biochim. Biophys. Acta. – 2007. – Vol. 1768, No. 11. – P. 2748-2756.
14. Bastien E., Schneider R., Hackbarth S., et al. PAMAM G4.5-chlorin e6 dendrimeric nanoparticles for enhanced photodynamic effects // Photochem. Photobiol. Sci. – 2015. – Vol. 14, No. 12. – P. 2203-2212.
15. Zorina T.E., Yankovsky I.V., Kravchenko I.E., et al. Evaluation of Phototoxicity and cytotoxicity for chlorin e6 ester derivatives and their liposomal forms // Biophysics. – 2015. – Vol. 60, No. 5. – P. 759-766.
16. Cunderlíková B., Gangeskar L., Moan J. Acid-base properties of chlorin e6: relation to cellular uptake // J. Photochem. Photobiol. B. – 1999. – Vol. 53, No. 1-3. – P. 81-90.
17. Zorin V.P. et al. Intraand intermembrane distribution of chlorin e6 derivatives // Proceedings SPIE. – 1994. – Vol. 2325. – P. 87-101.
18. Castano A.P., Demidova T.N., Hamblin M.R. Mechanisms in photodynamic therapy: part one-photosensitizers, photochemistry and cellular localization // Photodiagnosis Photodyn. Ther. – 2004. – Vol. 1, No. 4. – P. 279-293.
19. Jori G., Reddi E. The role of lipoproteins in the delivery of tumourtargeting photosensitizers // Int. J. Biochem. – 1993. – Vol. 25, No. 10. – P. 1369-1375.
20. Akhlynina T.V., Rosenkranz A.A., Jans D.A., Sobolev A.S. Insulinmediated intracellular targeting enhances the photodynamic activity of chlorin e6 // Cancer Res. – 1995. – Vol. 55, No. 5. – P. 1014-1019.
21. Oleinick N.L., Morris R.L., Belichenko I. The role of apoptosis in response to photodynamic therapy: what, where, why, and how // Photochem. Photobiol. Sci. – 2002. – Vol. 1, No. 1. – P. 1-21.
22. Gurinovich G.P., Zorina T.E., Melnov S.B., et al. Photodynamic activity of chlorin e6 and chlorin e6 ethylenediamide in vitro and in vivo // J. Photochem. Photobiol. B. – 1992. – Vol. 13, No. 1. – P. 51-57.
23. Sheleg S.V., Zhavrid E.A., Khodina T.V., et al. Photodynamic therapy with chlorin e(6) for skin metastases of melanoma // Photodermatol. Photoimmunol. Photomed. – 2004. – Vol. 20, No. 1. – P. 21-26.
24. Luo W., Liu R.S., Zhu J.G., et al. Subcellular location and photodynamic therapeutic effect of chlorin e6 in the human tongue squamous cell cancer Tca8113 cell line // Oncol. Lett. – 2015. – Vol. 9, No. 2. – P. 551-556.
25. West C.M., Moore J.V. Mechanisms behind the resistance of spheroids to photodynamic treatment: a flow cytometry study // Photochem. Photobiol. – 1992. – Vol. 55, No. 3. – P. 425-430.
26. Yuan A., Yang B., Wu J., et al. Dendritic nanoconjugates of photosensitizer for targeted photodynamic therapy // Acta Biomater. – 2015. – Vol. 21. – P. 63-73.
27. Gaio E., Scheglmann D., Reddi E., Moret F. Uptake and phototoxicity of Foscan®, Foslip® and Fospeg® in multicellular tumor spheroids // J. Photochem. Photobiol. B. – 2016. – Vol. 161. – P. 244-252.
28. Coutier S., Bezdetnaya L.N., Foster T.H., et al. Effect of irradiation fluence rate on the efficacy of photodynamic therapy and tumor oxygenation in meta-tetra (hydroxyphenyl) chlorin (mTHPC)sensitized HT29 xenografts in nude mice // Radiat. Res. – 2002. – Vol. 158, No. 3. – P. 339-345.
Рецензия
Для цитирования:
Фаррахова Д.С., Яковец М.В., Лощенов В.Б., Bolotine L.N., Зорин В.П. ИССЛЕДОВАНИЕ РАСПРЕДЕЛЕНИЯ ХЛОРИНОВЫХ ФОТОСЕНСИБИЛИЗАТОРОВ В ДВУХМЕРНЫХ И ТРЕХМЕРНЫХ КЛЕТОЧНЫХ КУЛЬТУРАХ. Biomedical Photonics. 2017;6(2):4-11. https://doi.org/10.24931/2413-9432-2017-6-2-4-11
For citation:
Farrakhova D.S., Yakavets I.V., Loschenov V.B., Bolotine L.N., Zorin V.P. INVESTIGATION OF CHLORIN PHOTOSENSITIZERS DISTRIBUTION IN MONOLAYER AND SPHEROID CELL CULTURES. Biomedical Photonics. 2017;6(2):4-11. (In Russ.) https://doi.org/10.24931/2413-9432-2017-6-2-4-11
Просмотров: 1189
Послать статью по эл. почте 