Diéricon Sousa Cordeiro, Eduardo Sérgio de Souza, Cássia Alessandra Marquezin
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引用次数: 0
Abstract
In this study, the sphere-to-rod transition in sodium dodecyl sulfate (SDS) micelles was induced by increasing the ionic strength of the medium. This transition was monitored through the fluorescence of the lipophilic probe 2-amino-N-hexadecyl-benzamide (AHBA), which has a 16-carbon hydrocarbon chain and aggregates in aqueous solution. AHBA fluorescence parameters, such as emission intensity, spectral position, lifetime, and steady-state anisotropy, were monitored to understand the probe's behavior in aqueous solution as a function of ionic strength. The results showed that the addition of NaCl induces a spectral red shift in AHBA fluorescence, suggesting a repositioning of the probe within its aggregate. Fluorescence quenching experiments were also conducted using the Co2+ ion as a quencher of AHBA fluorescence, both when free in aqueous solution and at different salt concentrations. The quenching results revealed the presence of two distinct AHBA populations, each with different access to Co2+. The Stern-Volmer plots for low Co2+ concentrations, where quenching primarily affects the population most exposed to Co2+, indicated that NaCl slightly reduces the accessibility of this population to the quencher. Finally, the sphere-to-rod transition in SDS micelles was monitored through fluorescence quenching assays. The Stern-Volmer plots showed a dependence on the ionic strength of the medium, indicating that the change in the micelle shape occurs between 0.2 M and 0.3 M NaCl. Once the rod shape is reached, the quenching constant assumes lower values, suggesting that AHBA becomes more inserted into the micelles, with reduced access to Co2+.
期刊介绍:
Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.