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Synthesis of new binary porphyrin–cyanine conjugates and their self-aggregation in organic-aqueous media

Kseniya Aleksandrovna Zhdanova 1
Kseniya Aleksandrovna Zhdanova
Artem Victorovich Ezhov 1
Artem Victorovich Ezhov
Natal'ya Aleksandrovna Bragina 1
Natal'ya Aleksandrovna Bragina
Andrey Fedorovich Mironov 1
Andrey Fedorovich Mironov
Published 2018-11-01
CommunicationVolume 28, Issue 6, 626-628
6
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Zhdanova K. A. et al. Synthesis of new binary porphyrin–cyanine conjugates and their self-aggregation in organic-aqueous media // Mendeleev Communications. 2018. Vol. 28. No. 6. pp. 626-628.
GOST all authors (up to 50) Copy
Zhdanova K. A., Ezhov A. V., Bragina N. A., Mironov A. F. Synthesis of new binary porphyrin–cyanine conjugates and their self-aggregation in organic-aqueous media // Mendeleev Communications. 2018. Vol. 28. No. 6. pp. 626-628.
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TY - JOUR
DO - 10.1016/j.mencom.2018.11.021
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.11.021
TI - Synthesis of new binary porphyrin–cyanine conjugates and their self-aggregation in organic-aqueous media
T2 - Mendeleev Communications
AU - Zhdanova, Kseniya Aleksandrovna
AU - Ezhov, Artem Victorovich
AU - Bragina, Natal'ya Aleksandrovna
AU - Mironov, Andrey Fedorovich
PY - 2018
DA - 2018/11/01
PB - Mendeleev Communications
SP - 626-628
IS - 6
VL - 28
ER -
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@article{2018_Zhdanova,
author = {Kseniya Aleksandrovna Zhdanova and Artem Victorovich Ezhov and Natal'ya Aleksandrovna Bragina and Andrey Fedorovich Mironov},
title = {Synthesis of new binary porphyrin–cyanine conjugates and their self-aggregation in organic-aqueous media},
journal = {Mendeleev Communications},
year = {2018},
volume = {28},
publisher = {Mendeleev Communications},
month = {Nov},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.11.021},
number = {6},
pages = {626--628},
doi = {10.1016/j.mencom.2018.11.021}
}
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Zhdanova, Kseniya Aleksandrovna, et al. “Synthesis of new binary porphyrin–cyanine conjugates and their self-aggregation in organic-aqueous media.” Mendeleev Communications, vol. 28, no. 6, Nov. 2018, pp. 626-628. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.11.021.

Abstract

New amphiphilic conjugates of porphyrins and cyanine dye Cy5COOH were prepared by the creation of ester or amide bond between Cy5-carboxylic acid and hydroxy- or amino-substituted porphyrins. Study of self-aggregation of these conjugates in aqueous-organic media by dynamic light scattering and UV-VIS spectroscopy showed that the conjugates form micelles in THF–H2O with different ratios.

References

1.
The potential of photodynamic therapy (PDT)—Experimental investigations and clinical use
Oniszczuk A., Wojtunik-Kulesza K.A., Oniszczuk T., Kasprzak K.
Biomedicine and Pharmacotherapy, 2016
2.
Imaging and Photodynamic Therapy: Mechanisms, Monitoring, and Optimization
Celli J.P., Spring B.Q., Rizvi I., Evans C.L., Samkoe K.S., Verma S., Pogue B.W., Hasan T.
Chemical Reviews, 2010
3.
Nanoparticles in Photodynamic Therapy
Lucky S.S., Soo K.C., Zhang Y.
Chemical Reviews, 2015
5.
Folic acid and its derivatives for targeted photodynamic therapy of cancer
Suvorov N.V., Mironov A.F., Grin M.A.
Russian Chemical Bulletin, 2017
6.
Gushchina O.I., Gramma V.A., Larkina E.A., Mironov A.F.
Mendeleev Communications, 2017
7.
Functional nanomaterials for phototherapies of cancer.
Cheng L., Wang C., Feng L., Yang K., Liu Z.
Chemical Reviews, 2014
8.
Active Targeting of Nano-Photosensitizer Delivery Systems for Photodynamic Therapy of Cancer Stem Cells
Lin L., Xiong L., Wen Y., Lei S., Deng X., Liu Z., Chen W., Miao X.
Journal of Biomedical Nanotechnology, 2014
9.
A novel bacteriochlorin-styrylnaphthalimide conjugate for simultaneous photodynamic therapy and fluorescence imaging.
Panchenko P.A., Grin M.A., Fedorova O.A., Zakharko M.A., Pritmov D.A., Mironov A.F., Arkhipova A.N., Fedorov Y.V., Jonusauskas G., Yakubovskaya R.I., Morozova N.B., Ignatova A.A., Feofanov A.V.
Physical Chemistry Chemical Physics, 2017
12.
A Novel Approach to a Bifunctional Photosensitizer for Tumor Imaging and Phototherapy
Chen Y., Gryshuk A., Achilefu S., Ohulchansky T., Potter W., Zhong T., Morgan J., Chance B., Prasad P.N., Henderson B.W., Oseroff A., Pandey R.K.
Bioconjugate Chemistry, 2005
13.
James N.S., Ohulchanskyy T.Y., Chen Y., Joshi P., Zheng X., Goswami L.N., Pandey R.K.
Theranostics, 2013
14.
Photosensitizer (PS)-cyanine dye (CD) conjugates: Impact of the linkers joining the PS and CD moieties and their orientation in tumor-uptake and photodynamic therapy (PDT).
James N.S., Joshi P., Ohulchanskyy T.Y., Chen Y., Tabaczynski W., Durrani F., Shibata M., Pandey R.K.
European Journal of Medicinal Chemistry, 2016
15.
Strategies for Delivering Porphyrinoid-Based Photosensitizers in Therapeutic Applications
Samaroo D., Perez E., Aggarwal A., Wills A., O'Connor N.
Therapeutic Delivery, 2014
16.
Thioglycosylated cationic porphyrins––convenient synthesis and photodynamic activity in vitro
17.
Lebedeva N.S., Yurina E.S., Gubarev Y.A., Koifman O.I.
Mendeleev Communications, 2017
18.
Self-Organization of Polar Porphyrinoids
Babu S.S., Bonifazi D.
ChemPlusChem, 2014
19.
Synthesis, properties and self-organization ofmeso-arylporphyrins with higher alkyl substituents
Bragina N.A., Zhdanova K.A., Mironov A.F.
Russian Chemical Reviews, 2016
20.
A Convenient Synthesis of Cyanine Dyes: Reagents for the Labeling of Biomolecules
Kvach M.V., Ustinov A.V., Stepanova I.A., Malakhov A.D., Skorobogatyi M.V., Shmanai V.V., Korshun V.A.
European Journal of Organic Chemistry, 2008
21.
Intramolecular Dimers:  A New Strategy to Fluorescence Quenching in Dual-Labeled Oligonucleotide Probes
Johansson M.K., Fidder H., Dick D., Cook R.M.
Journal of the American Chemical Society, 2002
23.
Fomina M.V., Nikiforov A.S., Vedernikov A.I., Kurchavov N.A., Gromov S.P.
Mendeleev Communications, 2014
24.
NEW PEGYLATED UNSYMMETRICAL MESO-ARYLPORPHYRINS AS POTENTIAL PHOTOSENSITIZERS
Zhdanova K.A., Cherepanova K.S., Bragina N.A., Mironov A.F.
Macroheterocycles, 2016
25.
Synthesis of amino-containing meso-aryl-substituted porphyrins and their conjugates with the closo-decaborate anion
Zhdanova K.A., Zhdanov A.P., Ezhov A.V., Bragina N.A., Zhizhin K.Y., Ushakova I.P., Mironov A.F., Kuznetsov N.T.
Russian Chemical Bulletin, 2014
26.
Zhdanova K.A., Bragina N.A., Bagratashvili V.N., Timashev P.S., Mironov A.F.
Mendeleev Communications, 2014
27.
Synthesis of lipophilic tetraphenylporphyrins to design lipid-porphyrin ensembles
Fedulova I.N., Bragina N.A., Novikov N.V., Ugol’nikova O.A., Mironov A.F.
Russian Journal of Bioorganic Chemistry, 2007
28.
Synthesis and reactivities of 3-Indocyanine-green-acyl-1,3-thiazolidine-2-thione (ICG-ATT) as a new near-infrared fluorescent-labeling reagent
Hirata T., Kogiso H., Morimoto K., Miyamoto S., Taue H., Sano S., Muguruma N., Ito S., Nagao Y.
Bioorganic and Medicinal Chemistry, 1998
29.
Practical syntheses of dyes for difference gel electrophoresis
Jung M.E., Kim W.
Bioorganic and Medicinal Chemistry, 2006