Aggregation of t10,c12 conjugated linoleic Acid in presence of natural and modified cyclodextrins. A physicochemical, thermal and computational analysis.

Chem Phys Lipids

Department of Biochemistry and Molecular Biology-A, Faculty of Biology, University of Murcia, Campus de Espinardo, 30071, Murcia, Spain. Electronic address:

Published: April 2017

AI Article Synopsis

  • The aggregation behavior of t10,c12 Conjugated linoleic acid (t10,c12-CLA) was investigated for the first time, revealing a critical micelle concentration (c.m.c.) of 25μM at pH 8 and 25°C.
  • The encapsulation with cyclodextrins (CDs) demonstrated a 1:1 binding ratio, with complexation constants varying based on the type of CD, pH, and temperature, with Hydroxypropyl-beta-Cyclodextrin (HPβCD) being the most effective.
  • Additionally, the study explored how pH and temperature affect the stability of the t10,c12-CLA-HPβCD complex and included molecular docking calculations

Article Abstract

In this work the aggregation behavior of t10,c12 Conjugated linoleic acid (t10,c12-CLA) is presented for first time. The results show a c.m.c. of 25μM at pH 8 and 25°C. The encapsulation process with cyclodextrins (CDs) presented a 1:1 stoichiometry in all cases studied but the complexation constants were strongly dependent on the type of CDs used, the pH and temperature. Hydroxypropyl-beta-Cyclodextrin (HPβCD) was the best CD studied for encapsulating t10,c12-CLA. The resulting t10,c12-CLA-HPβCD complex showed a very high dependency on pH, which explains why a pK of 4.08 was found for first time, which was very close to the simulated value. Furthermore, the effect of temperature on the t10,c12-CLA-HPβCD was studied. The complexation constant (K) showed an increase behavior with the temperature. In addition, molecular docking calculations provided further insights into how the different interactions influence the complexation constant. Finally, a comparative study with rumenic acid, an isomer, was carried out.

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Source
http://dx.doi.org/10.1016/j.chemphyslip.2017.03.008DOI Listing

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