Colloids and Surfaces B: Biointerfaces, volume 216, pages 112532

Spanning BODIPY fluorescence with self-assembled micellar clusters.

Solomonov Alexey V. ¹

Marfin Yuriy S. ²

Tesler Alexander ³

Merkushev Dmitry A ²

Bogatyreva Elizaveta A ²

Antina Elena V ⁴

Rumyantsev E.V. ^{2, 5}

Shimanovich Ulyana ¹

Hide authors affiliations Show authors affiliations: 5 affiliations

Department of Molecular Chemistry and Materials Science, Faculty of Chemistry, Weizmann Institute of Science, 7610001 Rehovot, Israel |

Department of Inorganic Chemistry, Ivanovo State University of Chemistry and Technology, 7 Sheremetevskij prosp., 153000 Ivanovo, Russian Federation |

Department of Materials Science and Engineering, Friedrich-Alexander University Erlangen-Nuremberg, 7 Martensstrasse, Erlangen 91056 Germany |

⁴

G.A. Krestov Institute of Solution Chemistry of the Russian Academy of Sciences, 1 Akademicheskaya St., 153045 Ivanovo, Russian Federation |

⁵

Ivanovo State Polytechnical University, 20 8th Marta St., 153037 Ivanovo, Russian Federation |

Publication type: Journal Article

Publication date: 2022-08-01

Elsevier

Journal: Colloids and Surfaces B: Biointerfaces

Quartile SCImago

Quartile WOS

Impact factor: 5.8

ISSN: 09277765, 18734367

DOI: 10.1016/j.colsurfb.2022.112532

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Physical and Theoretical Chemistry

General Medicine

Colloid and Surface Chemistry

Biotechnology

Surfaces and Interfaces

Abstract

BODIPY dyes possess favorable optical properties for a variety of applications including in vivo and in vitro diagnostics. However, their utilization might be limited by their water insolubility and incompatibility with chemical modifications, resulting in low aggregation stability. Here, we outline the route for addressing this issue. We have demonstrated two approaches, based on dye entrapment in micellar coordination clusters (MCCs); this provides a general solution for water solubility as well as aggregation stability of the seven BODIPY derivatives. These derivatives have various bulky aromatic substituents in the 2,3,5,6- and meso-positions and can rotate relative to a dipyrrin core, which also provides molecular rotor properties. The molecular structural features and the presence of aromatic groups allows BODIPY dyes to be used as "supporting molecules", thus promoting micelle-micelle interaction and micellar network stabilization. In the second approach, self-micellization, following BODIPY use, leads to MCC formation without the use of any mediators, including chelators and/or metal ions. In both approaches, BODIPY exhibits an excellent optical response, at a concentration beyond its solubilization limit in aqueous media and without undesired crystallization. The suggested approaches represent systems used to encapsulate BODIPY in a capsule-based surfactant environment, enabling one to track the aggregation of BODIPY; these approaches represent an alternative system to study and apply BODIPY's molecular rotor properties. The stabilized compounds, i.e., the BODIPY-loaded MCCs, provide a unique feature of permeability to hydrophilic ligand-switching proteins such as BSA; they exhibit a bright "turn-on" fluorescence signal within the clusters via macromolecular complexation, thus expanding the possibilities of water-soluble BODIPY-loaded MCCs utilization for functional indicators.

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Journal of the American Chemical Society	Journal of the American Chemical Society, 1, 25% Journal of the American Chemical Society 1 publication, 25%
Journal of Molecular Liquids	Journal of Molecular Liquids, 1, 25% Journal of Molecular Liquids 1 publication, 25%
Dyes and Pigments	Dyes and Pigments, 1, 25% Dyes and Pigments 1 publication, 25%
Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya	Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya, 1, 25% Izvestiya Vysshikh Uchebnykh Zavedenii, Seriya Khimiya i Khimicheskaya Tekhnologiya 1 publication, 25%
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Elsevier	Elsevier, 2, 50% Elsevier 2 publications, 50%
American Chemical Society (ACS)	American Chemical Society (ACS), 1, 25% American Chemical Society (ACS) 1 publication, 25%
Ivanovo State University of Chemistry and Technology	Ivanovo State University of Chemistry and Technology, 1, 25% Ivanovo State University of Chemistry and Technology 1 publication, 25%
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Solomonov A. V. et al. Spanning BODIPY fluorescence with self-assembled micellar clusters. // Colloids and Surfaces B: Biointerfaces. 2022. Vol. 216. p. 112532.

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Solomonov A. V., Marfin Y. S., Tesler A., Merkushev D. A., Bogatyreva E. A., Antina E. V., Rumyantsev E., Shimanovich U. Spanning BODIPY fluorescence with self-assembled micellar clusters. // Colloids and Surfaces B: Biointerfaces. 2022. Vol. 216. p. 112532.

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RIS Copy

TY - JOUR

DO - 10.1016/j.colsurfb.2022.112532

UR - https://doi.org/10.1016%2Fj.colsurfb.2022.112532

TI - Spanning BODIPY fluorescence with self-assembled micellar clusters.

T2 - Colloids and Surfaces B: Biointerfaces

AU - Solomonov, Alexey V.

AU - Marfin, Yuriy S.

AU - Tesler, Alexander

AU - Merkushev, Dmitry A

AU - Bogatyreva, Elizaveta A

AU - Antina, Elena V

AU - Rumyantsev, E.V.

AU - Shimanovich, Ulyana

PY - 2022

DA - 2022/08/01 00:00:00

PB - Elsevier

SP - 112532

VL - 216

SN - 0927-7765

SN - 1873-4367

ER -

BibTex

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@article{2022_Solomonov,

author = {Alexey V. Solomonov and Yuriy S. Marfin and Alexander Tesler and Dmitry A Merkushev and Elizaveta A Bogatyreva and Elena V Antina and E.V. Rumyantsev and Ulyana Shimanovich},

title = {Spanning BODIPY fluorescence with self-assembled micellar clusters.},

journal = {Colloids and Surfaces B: Biointerfaces},

year = {2022},

volume = {216},

publisher = {Elsevier},

month = {aug},

url = {https://doi.org/10.1016%2Fj.colsurfb.2022.112532},

pages = {112532},

doi = {10.1016/j.colsurfb.2022.112532}

}

Found error?

Publisher

Elsevier

Journal

Colloids and Surfaces B: Biointerfaces

Quartile SCImago

Quartile WOS

Impact factor

5.8

ISSN

09277765 (Print)
18734367 (Electronic)

Labs

Chemistry and molecular photonics of dipyrromethene dyes and phosphors

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