4.7 Article

Hyaluronan interactions with cationic surfactants-Insights from fluorescence resonance energy transfer and anisotropy techniques

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
Volume 211, Issue -, Pages 107-115

Publisher

ELSEVIER
DOI: 10.1016/j.ijbiomac.2022.05.067

Keywords

Fluorescence anisotropy; Fo ?rster resonance energy transfer; Hyaluronan; Surfactants

Funding

  1. Czech Science Foundation [19-14024J]
  2. Ministry of Science and Technology, Taiwan [MOST108-2923-E-006-006-MY3]

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This study investigated the interactions between hyaluronan and micelles formed by cationic surfactants using fluorescence resonance energy transfer (FRET). The results showed that the addition of hyaluronan led to the formation of a pearl necklace structure with smaller micelles compared to pure surfactant. This research is of significance for the formulation of drug delivery systems.
Interactions of hyaluronan with micelles formed by cationic surfactants were studied by the time-resolved measurement of fluorescence resonance energy transfer (FRET) using perylene and fluorescein as probes. Two surfactants were studied - Cetyltrimethylammonium bromide (CTAB) and Septonex. In pure micellar solutions, the same values of FRET efficiency were found for both surfactants, but values for the binding of the probe pair were lower for Septonex micelles than in the case of CTAB. This was attributed to steric effects of the carbethoxy group in the Septonex polar head. Upon the addition of hyaluronan, decreased FRET efficiency and increased binding were detected in comparison with pure surfactants. To resolve the structure of the formed aggregates, steady state and time-resolved fluorescence anisotropy was employed as an additional technique. All results indicated that cationic micelles bind to hyaluronan forming a pearl necklace structure with micelles of smaller size compared to pure surfactant. Besides theoretical interest, the studied polyelectrolyte-surfactant system may be interesting for the formulation of drug delivery systems.

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