The Relaxation Behavior of Water Confined in AOT-Based Reverse Micelles Under Temperature-Induced Clustering.

Int J Mol Sci

Kazan Institute of Biochemistry and Biophysics, FRC Kazan Scientific Center, Russian Academy of Sciences, Lobachevsky Str. 2/31, 420111 Kazan, Russia.

Published: July 2025


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Relaxation behavior of water confined in reverse micelles under temperature-induced micelle clustering is undertaken using broadband dielectric spectroscopy in frequency range 1 Hz-20 GHz. All microemulsion systems with sufficiently noticeable micelle water pool (water/surfactant molar ratio > 10) depict three relaxation processes, in low, high and microwave frequencies, anchoring with relaxation of shell (bound) water, orientation of surfactant anions at water-surfactant interface and relaxation of bulk water confined in reverse micelles. The analysis of dielectric relaxation processes in AOT-based w/o microemulsions under temperature induced clustering of reverse micelles were made according to structural information obtained in NMR and conductometry experiments. The "wait and switch" relaxation mechanism was applied for the explanation of results for water in the bound and bulk states under spatial limitation in reverse micelles. It was shown that surfactant layer predominantly influences the bound water. The properties of water close to AOT interface are determined by strong interactions between water and ionic AOT molecules, which perturb water H-bonding network. The decrease in micelle size causes a weakening of hydrogen bonds, deformation of its steric network and reduction in co-operative relaxation effects.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12346517PMC
http://dx.doi.org/10.3390/ijms26157152DOI Listing

Publication Analysis

Top Keywords

reverse micelles
20
water confined
12
water
10
relaxation
8
relaxation behavior
8
behavior water
8
micelles temperature-induced
8
confined reverse
8
relaxation processes
8
bound water
8

Similar Publications

The inhibition of dependent glutamine metabolism is an effective treatment for triple-negative breast cancer (TNBC) starvation, but it is limited by compensatory glycolysis and inadequate delivery efficiency. Herein, we construct a pH-responsive size/charge-reprogrammed micelle with hierarchical delivery characteristics for TNBC suppression with glutamine depletion and vessel blockade. It consists of a positively charged prodrug micelle chemically grafted with the glutamine transport inhibitor V9302 as the inner core layer, the neovascular disruptor CA4P adsorbed in the middle layer, and a pH-responsive peelable polymer as the outer shell.

View Article and Find Full Text PDF

Molecular Insights into the Reversible Mechanisms of CO-Switchable Surfactant Solubilization and Emulsification.

Langmuir

September 2025

Polymer Research Institute, State Key Laboratory of Advanced Polymer Materials, Sichuan University, Chengdu 610065, China.

Switchable surfactants exhibit broad application potential due to their reversible response to external stimuli. The reversible mechanism of the CO-switchable surfactant ('-dodecyl-, -dimethyl-acetamidines, DDA) solubilization polycyclic aromatic hydrocarbons (PAHs) and the microscopic dynamic behavior of emulsification/demulsification were systematically studied using coarse-grained molecular dynamics simulations. The dynamic transition processes of protonation (DDA to DDA) and deprotonation (DDA to DDA) were successfully simulated.

View Article and Find Full Text PDF

Time-Resolved Small-Angle X-Ray Studies of Spherical Micelle Formation and Growth During Polymerization-Induced Self-Assembly in Polar Solvents.

Small

September 2025

South China Advanced Institute for Soft Matter Science and Technology, School of Emergent Soft Matter, Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices, Guangdong Basic Research Center of Excellence for Energy and Information Polymer Materials, South Chi

Self-assembled poly(2-dimethylaminoethyl methacrylate)-poly(2-(diisopropylamino)ethyl methacrylate) (PDMA-PDPA) diblock copolymer nanoparticles are widely employed in biological applications, driving the need for a robust and scalable production method. Although polymerization-induced self-assembly (PISA) enables efficient nanoparticle synthesis at high solids content, its research and application to PDMA-PDPA are limited, likely due to kinetic trapping. Leveraging our recently developed generic time-resolved small-angle X-ray scattering (TR-SAXS) approach for PISA in non-polar media, a reversible addition-fragmentation chain transfer-mediated PDMA-PDPA PISA process in polar solvent that produces spherical micelles is examined.

View Article and Find Full Text PDF

This work reports the nanoscale micellar formation in single and mixed surfactant systems by combining an amphiphilic graft copolymer, Soluplus® (primary surfactant), blended with other polyoxyethylene (POE)-based nonionic surfactants such as Kolliphor® HS15, Kolliphor® EL, Tween-80, TPGS®, and Pluronics® P123 in an aqueous solution environment. The solution behaviour of these surfactants as a single system were analyzed in a wide range of surfactant concentrations and temperatures. Rheological measurements revealed distinct solution behaviour in the case of Soluplus®, ranging from low-viscosity () and fluid-like behavior at ≤20% w/v to a highly viscous state at ≥90% w/v, where the loss modulus ('') exceeded the storage modulus (').

View Article and Find Full Text PDF

Lung cancer remains the leading cause of cancer-related deaths worldwide, with limited curative options, particularly in advanced stages. Lipid-based nanocarriers, including liposomes, solid lipid nanoparticles (SLNs), nanostructured lipid carriers (NLCs), and lipid nanocapsules (LNCs), have emerged as promising drug delivery platforms owing to their biocompatibility, versatility, and potential for pulmonary administration. This review highlights recent advances in lipid nanocarriers for lung cancer therapy, with a particular focus on NLCs and LNCs.

View Article and Find Full Text PDF