Evaluating the suitability of six hydrophobic natural eutectic solvents as the internal phase in a cosmetic cream formulation

Abstract Objective This work evaluates whether hydrophobic natural eutectic solvents can replace the conventional oil phase in cosmetic creams while maintaining or improving physicochemical stability, rheological structure, and sensory performance. The goal is to develop formulations that combine sustainability, regulatory compliance, and sensory performance while remaining compatible with standard low‐energy manufacturing processes. Methods Six HNESs systems composed of regulation‐compliant fatty acids, menthol, and alkane diols were characterized for viscosity, density, and refractive index. Model oil‐in‐water creams were prepared using cold homogenization to ensure scalability and energy efficiency. Emulsion stability was assessed over 30 days in accelerated ageing conditions using multiple light scattering and pH tracking; rheology was evaluated via flow curves and strain sweep tests; applicative sensory properties (spreading resistance, gloss, stickiness, residual film wettability) were instrumentally measured on a non‐biological skin surrogate. Results Solvent composition governed emulsion behaviour. Fatty acid‐based systems produced small, stable droplets, low bulk viscosity, and favourable sensory attributes (high lubrication, reduced stickiness), while maintaining dermatologically acceptable pH. Menthol‐containing systems exhibited higher viscosities and strong gel‐like networks but showed physical instability under storage. Alkane diol‐rich systems improved lubrication and gloss yet displayed larger droplet growth and pH drift, indicating weaker long‐term stability. Across all creams, residual films decreased the water contact angle markedly, evidencing hydrophilic surface behaviour after application, and immediate gloss increased versus triglycerides control. Conclusion HNESs can function as structural oily phase substitutes in creams prepared by low‐energy processes, enabling sustainable, regulation‐compliant formulations with desirable sensory profiles. Fatty acid‐based systems offer the most robust balance of stability and user experience, whereas menthol‐ and alkane diol‐rich systems require compositional optimization to mitigate storage instability while preserving sensory benefits.

Authors

Institutions

Publication Details

Journal
International Journal of Cosmetic Science
Published
2026-03-29
DOI
https://doi.org/10.1111/ics.70097
Primary Topic
Ionic liquids properties and applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Evaluating the suitability of six hydrophobic natural eutectic solvents as the internal phase in a cosmetic cream formulation

Michel Grisel, Elsa Vrignaud, Ecaterina Gore, Xavier Perse et al.
International Journal of Cosmetic Science
Ionic liquids properties and applications
article

Evaluating the suitability of six hydrophobic natural eutectic solvents as the internal phase in a cosmetic cream formulation

Michel Grisel, Elsa Vrignaud, Ecaterina Gore, Xavier Perse, Emilie Munnier, Leslie Boudesocque‐Delaye, Alexis Verger, Salima Bouderbala, R. Grard
article en

Abstract

Abstract Objective This work evaluates whether hydrophobic natural eutectic solvents can replace the conventional oil phase in cosmetic creams while maintaining or improving physicochemical stability, rheological structure, and sensory performance. The goal is to develop formulations that combine sustainability, regulatory compliance, and sensory performance while remaining compatible with standard low‐energy manufacturing processes. Methods Six HNESs systems composed of regulation‐compliant fatty acids, menthol, and alkane diols were characterized for viscosity, density, and refractive index. Model oil‐in‐water creams were prepared using cold homogenization to ensure scalability and energy efficiency. Emulsion stability was assessed over 30 days in accelerated ageing conditions using multiple light scattering and pH tracking; rheology was evaluated via flow curves and strain sweep tests; applicative sensory properties (spreading resistance, gloss, stickiness, residual film wettability) were instrumentally measured on a non‐biological skin surrogate. Results Solvent composition governed emulsion behaviour. Fatty acid‐based systems produced small, stable droplets, low bulk viscosity, and favourable sensory attributes (high lubrication, reduced stickiness), while maintaining dermatologically acceptable pH. Menthol‐containing systems exhibited higher viscosities and strong gel‐like networks but showed physical instability under storage. Alkane diol‐rich systems improved lubrication and gloss yet displayed larger droplet growth and pH drift, indicating weaker long‐term stability. Across all creams, residual films decreased the water contact angle markedly, evidencing hydrophilic surface behaviour after application, and immediate gloss increased versus triglycerides control. Conclusion HNESs can function as structural oily phase substitutes in creams prepared by low‐energy processes, enabling sustainable, regulation‐compliant formulations with desirable sensory profiles. Fatty acid‐based systems offer the most robust balance of stability and user experience, whereas menthol‐ and alkane diol‐rich systems require compositional optimization to mitigate storage instability while preserving sensory benefits.

International Journal of Cosmetic Science
Université de Tours (FR), Centre National de la Recherche Scientifique (FR), Université Le Havre Normandie (FR), Normandie Université (FR)
Affordable and clean energy
Openalex Percentile: Top 7%
Ionic liquids properties and applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.