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Understanding Molecular-Level Interactions Between the Soluplus-Bile Salts Mixed Micellar System
Virendra Prajapati1, Arup Kumar Ghosh1, Debes Ray2
1Department of Chemistry, Sardar Vallabhbhai National Institute of Technology (SVNIT), Ichchhanath Dumas Road, Keval Chowk, Surat, Gujarat 395007, India.
This study explores Soluplus copolymer micellization with bile salts, enhancing its temperature stability. Bile salts like sodium deoxycholate improve Soluplus
Area of Science:
- Polymer Science
- Colloid and Surface Chemistry
- Materials Science
Background:
- Soluplus, a graft copolymer, exhibits amphiphilic properties suitable for micelle formation.
- Its low cloud point (CP) limits applications in temperature-sensitive formulations.
- Bile salts are biologically relevant surfactants with potential to modify micellar properties.
Purpose of the Study:
- To investigate the micellization behavior of Soluplus in the presence of sodium cholate (NaC) and sodium deoxycholate (NaDC).
- To enhance the cloud point (CP) of Soluplus for broader formulation applications.
- To elucidate the molecular interactions and stability of Soluplus-bile salt mixed micelles.
Main Methods:
- Cloud point (CP) measurements.
- Dynamic Light Scattering (DLS) for micelle size and transitions.
- Small-Angle Neutron Scattering (SANS) for micellar morphology.
- Density Functional Theory (DFT) and Quantum Mechanical (QM) calculations.
- Fourier Transform Infrared (FTIR) spectroscopy.
Main Results:
- NaC and NaDC significantly increase the CP of Soluplus, with NaDC showing a greater effect.
- Mixed micelles exhibit concentration-dependent transitions and defined morphologies.
- DFT and QM analyses reveal weak intermolecular interactions and assess compatibility.
- Soluplus forms micelles with CMC ~7.6 mg/L, hydrodynamic diameter ~70-90 nm.
Conclusions:
- Bile salts effectively enhance the thermal stability of Soluplus micelles.
- Mixed Soluplus-bile salt systems offer tunable properties for advanced formulations.
- The study provides insights into the self-assembly and interactions of amphiphilic copolymers with biological surfactants.
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