4.7 Article

Spanning BODIPY fluorescence with self-assembled micellar clusters

期刊

出版社

ELSEVIER
DOI: 10.1016/j.colsurfb.2022.112532

关键词

Self-assembly; Surfactants; Micellar clusters; BODIPY dyes; Encapsulation; Proteins

资金

  1. Government of the State of Israel at Ariel University, Israel [19-73-10107]
  2. Russian Science Foundation [1504994]
  3. Gruber Foundation
  4. Nella and Leon Benoziyo Center for Neurological Diseases
  5. Alon fellowship (Israeli Council for Higher Education)
  6. Perlman family
  7. Anita James Rosen Foundation
  8. Weizmann Institute of Science, Israel
  9. Minerva Foundation

向作者/读者索取更多资源

This paper outlines two approaches to address the water insolubility and low aggregation stability of BODIPY dyes. By entrapping the dye in micellar coordination clusters or through self-micellization, the water solubility and aggregation stability of BODIPY can be achieved. These approaches also demonstrate the potential use of BODIPY as a supporting molecule and for functional indicators.
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, selfmicellization, 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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