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Published on: March 24, 2018
Food volatile compounds facilitating HII mesophase formation: solubilization and stability
Natali Amar-Zrihen1, Abraham Aserin, Nissim Garti
1The Ratner Chair of Chemistry, Casali Institute of Applied Chemistry, The Hebrew University of Jerusalem, Jerusalem, Israel.
Lipophilic food volatiles stabilize hexagonal (H(II)) mesophases in monoolein/water systems without solvents. These flavor compounds enhance structural stability and can be released at elevated temperatures.
Area of Science:
- Food Science
- Materials Science
- Physical Chemistry
Background:
- Food volatile molecules are crucial for flavor and aroma.
- Controlling their release and stability is essential for food product development.
- Self-assembling lipidic systems offer potential for encapsulating and delivering volatile compounds.
Purpose of the Study:
- To investigate the solubilization of four lipophilic food volatile molecules in monoolein/water systems.
- To determine the impact of these volatiles on the formation and stability of liquid crystalline mesophases.
- To explore the potential for controlled release of food volatiles from these mesophases.
Main Methods:
- Solubilization of phenylacetaldehyde, 2,6-dimethyl-5-heptenal, linalool, and trans-4-decenal in binary monoolein/water mixtures.
- Formation and characterization of liquid crystalline phases (lamellar, cubic, hexagonal H(II)) using techniques not specified but implied by phase analysis.
- Analysis of phase transitions and lattice parameters in response to temperature and composition.
Main Results:
- High solubilization loads of food volatiles (10.0-12.6 wt%) were achieved, forming stable reverse hexagonal (H(II)) mesophases without solvents.
- Phenylacetaldehyde formed lamellar and cubic phases, while linalool, 2,6-dimethyl-5-heptenal, and trans-4-decenal induced a direct transition to stable H(II) mesophases.
- Lattice parameters varied with water content, temperature, and volatile concentration; trans-4-decenal yielded a more stable H(II) phase than linalool.
- The H(II) mesophase transformed into an isotropic micellar phase at 40-60 °C, enabling volatile release.
Conclusions:
- Lipophilic food volatiles can act as structure-directing agents in monoolein/water systems, forming stable H(II) mesophases.
- The chemical structure of the volatile influences the resulting mesophase and its stability.
- These self-assembling systems provide a promising platform for the controlled delivery and stabilization of food flavor compounds.
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