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Effect of Cis and Trans Double Bonds on Conformational Disordering of the Hydrocarbon Chain of Lipid, Unsaturated Monoacylglycerols, in the Lamellar Phase of a Binary System with Water

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Department of Chemistry, Graduate School of Pure and Applied Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8571, Japan
Cite this: J. Phys. Chem. B 2011, 115, 50, 14963–14968
Publication Date (Web):November 15, 2011
https://doi.org/10.1021/jp205881f
Copyright © 2011 American Chemical Society
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Abstract

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To clarify the influence of cis and trans double bonds on conformational disordering of unsaturated hydrocarbon-chain of lipids in bilayer formed in the binary system with water, calorimetric study was conducted for systems of unsaturated monoacylglycerols; monoolein (MO), monovaccenin (MV), and monoelaidin (ME). Heat capacities of the binary systems were measured by adiabatic calorimetry. The observed entropies of transition (ΔtrsS) from lamellar phase (Lα) to fluid isotropic (FI) phase are very small and depend on lipids: ΔtrsS of MO/water, MV/water, and ME/water were ca. 0.8 J K–1 (mol of lipid) –1, ca. 0.9 J K–1 (mol of lipid) –1, and ca. 0.4 J K–1 (mol of lipid) –1, respectively. These show that the conformational disordering of the hydrocarbon chain over gauche and trans conformations is suppresed in Lα phase. Through the comparison of ΔtrsS among the binary systems, the suppresed conformational disordering of hydrocarbon chain in the bilayer is discussed.

Cited By


This article is cited by 1 publications.

  1. Wye-Khay Fong, Tracey L. Hanley, Benjamin Thierry, Adam Tilley, Nigel Kirby, Lynne J. Waddington, Ben J. Boyd. Understanding the photothermal heating effect in non-lamellar liquid crystalline systems, and the design of new mixed lipid systems for photothermal on-demand drug delivery. Phys. Chem. Chem. Phys. 2014, 16 (45) , 24936-24953. https://doi.org/10.1039/C4CP03635B

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