Volume 83, Issue 8
Food Chemistry
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Interaction Between Phenolic Compounds and Lipase: The Influence of Solubility and Presence of Particles in the IC50 Value

Atma‐Sol Bustos

Corresponding Author

E-mail address: atma-sol.bustos@food.lth.se

Food Technology, Faculty of Engineering LTH, Lund Univ., PO Box 124, Lund, S‐221 00 Sweden

School of Chemistry, Faculty of Pure and Natural Sciences, Univ. Mayor de San Andrés, PO Box 303, La Paz, Bolivia

Direct inquiries to author Bustos (E‐mail: atma-sol.bustos@food.lth.se).Search for more papers by this author
Andreas Håkansson

Food Technology, Faculty of Engineering LTH, Lund Univ., PO Box 124, Lund, S‐221 00 Sweden

Food and Meal Science, Kristianstad Univ., PO Box 15, Kristianstad, S‐291 81 Sweden

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Javier A. Linares‐Pastén

Biotechnology, Faculty of Engineering LTH, Lund Univ., PO Box 117, Lund, S‐221 00 Sweden

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Jose M. Penarrieta

School of Chemistry, Faculty of Pure and Natural Sciences, Univ. Mayor de San Andrés, PO Box 303, La Paz, Bolivia

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Lars Nilsson

Food Technology, Faculty of Engineering LTH, Lund Univ., PO Box 124, Lund, S‐221 00 Sweden

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First published: 18 July 2018
Citations: 9

Abstract

Obesity is one of the principal human health problems and one of the main treatments against it is the inhibition of pancreatic lipase, the main responsible enzyme of lipid digestion. For that purpose, previous studies have tested several phenolic compounds against lipase, without considering their aggregation behavior in aqueous solutions. Because of this, the present study focuses on understanding how the solubility and the presence of particles affect the IC50 value of the interaction between lipase and phenolic compounds present in beverages like fruit juices and teas. Therefore, the inhibitory capacity against pancreatic lipase and the aggregate formation of 9 phenolic compounds (quercetin, rutin, myricetin, catechin, epigallocatechin gallate, cyanidin, caffeic acid, chlorogenic acid, and vanillic acid) were analyzed. The results obtained together with the solubility data from literature were treated by principal component analysis and indicate that the IC50 value does not correlate with the solubility or aggregate formation of the phenolic compounds. However, the IC50 values of phenolic compounds which aggregate during the assay conditions have low reproducibility. This study shows that the aggregate formation of phenolic compounds plays an important role during in vitro assays for pancreatic lipase inhibition and should be considered in future experiments as it can lead to false positive results. In terms of particle formation, the flavonoids investigated in this study are more prone to aggregation compared to the phenolic acids.

Number of times cited according to CrossRef: 9

  • Exploring Ulva australis Areschoug for possible biotechnological applications: In vitro antioxidant and enzymatic inhibitory properties, and fatty acids contents, Algal Research, 10.1016/j.algal.2020.101980, 50, (101980), (2020).
  • Digestive Enzyme Inhibition of Different Phenolic Fractions and Main Phenolic Compounds of Ultra-High-Pressure-Treated Palm Fruits: Interaction and Molecular Docking Analyses, Journal of Food Quality, 10.1155/2020/8811597, 2020, (1-10), (2020).
  • Interaction of quercetin and epigallocatechin gallate (EGCG) aggregates with pancreatic lipase under simplified intestinal conditions, PLOS ONE, 10.1371/journal.pone.0224853, 15, 4, (e0224853), (2020).
  • Vanillic acid as phospholipase A2 and proteases inhibitor: In vitro and computational analyses, Biotechnology and Applied Biochemistry, 10.1002/bab.1943, 0, 0, (2020).
  • Interaction between Myricetin Aggregates and Lipase under Simplified Intestinal Conditions, Foods, 10.3390/foods9060777, 9, 6, (777), (2020).
  • On-line immobilized trypsin microreactor for evaluating inhibitory activity of phenolic acids by capillary electrophoresis and molecular docking, Food Chemistry, 10.1016/j.foodchem.2019.125823, (125823), (2019).
  • Fabrication of pea protein-tannic acid complexes: Impact on formation, stability, and digestion of flaxseed oil emulsions, Food Chemistry, 10.1016/j.foodchem.2019.125828, (125828), (2019).
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  • Inhibition of Inositol Polyphosphate Kinases by Quercetin and Related Flavonoids: A Structure/Activity Analysis., Journal of Medicinal Chemistry, 10.1021/acs.jmedchem.8b01593, (2019).

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