Comparative behavior of protein or polysaccharide stabilized emulsion under in vitro gastrointestinal conditions

In the present work, an in vitro model digestion was used to compare the behavior of emulsions stabilized by proteins or polysaccharide upon digestion and to analyze its relationship with the kinetics and extent of lipid digestion. Oil/water emulsions were prepared using different emulsifiers (β-lac...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Bellesi, F.A., Martinez, M.J., Pizones Ruiz-Henestrosa, V.M., Pilosof, A.M.R.
Formato: JOUR
Materias:
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_0268005X_v52_n_p47_Bellesi
Aporte de:
id todo:paper_0268005X_v52_n_p47_Bellesi
record_format dspace
spelling todo:paper_0268005X_v52_n_p47_Bellesi2023-10-03T15:13:48Z Comparative behavior of protein or polysaccharide stabilized emulsion under in vitro gastrointestinal conditions Bellesi, F.A. Martinez, M.J. Pizones Ruiz-Henestrosa, V.M. Pilosof, A.M.R. Emulsion Interfacial film Lipid digestion In the present work, an in vitro model digestion was used to compare the behavior of emulsions stabilized by proteins or polysaccharide upon digestion and to analyze its relationship with the kinetics and extent of lipid digestion. Oil/water emulsions were prepared using different emulsifiers (β-lactoglobulin, soy protein isolate and hydroxypropylmethylcellulose (HPMC)). The emulsion digestion was carried out in two continuous stages at 37 °C: 1) under simulated gastric conditions (1 h) using pepsin and phosphatidylcholine (simulated gastric fluid: pH 2.5, NaCl, NaH<inf>2</inf>PO<inf>4</inf>, KCl and CaCl<inf>2</inf>) and 2) under simulated intestinal conditions (1 h) with bile salts, pancreatic lipase, trypsin and chymotrypsin (simulated intestinal fluid: pH 7.0, K<inf>2</inf>HPO<inf>4</inf>, NaCl and CaCl<inf>2</inf>). The changes in the particle size distributions, the interfacial area and their microstructures were analyzed as a function of the digestion time. The free fatty acid release during the simulated intestinal stage was also determined and an empirical model was fitted to estimate different kinetic parameters. Irrespective of the composition/structure of emulsions, the initial surface area was found to determine the initial rate of lipolysis. Soy protein was the protein that forms the most resistant emulsion to digestion, showing a degree of free fatty acid release similar to HPMC, which is a non digestible emulsifier. The results are discussed on the basis of the role of bile salts and its effect on oil/water interfaces. © 2015 Elsevier Ltd. Fil:Martinez, M.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Pilosof, A.M.R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_0268005X_v52_n_p47_Bellesi
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Emulsion
Interfacial film
Lipid digestion
spellingShingle Emulsion
Interfacial film
Lipid digestion
Bellesi, F.A.
Martinez, M.J.
Pizones Ruiz-Henestrosa, V.M.
Pilosof, A.M.R.
Comparative behavior of protein or polysaccharide stabilized emulsion under in vitro gastrointestinal conditions
topic_facet Emulsion
Interfacial film
Lipid digestion
description In the present work, an in vitro model digestion was used to compare the behavior of emulsions stabilized by proteins or polysaccharide upon digestion and to analyze its relationship with the kinetics and extent of lipid digestion. Oil/water emulsions were prepared using different emulsifiers (β-lactoglobulin, soy protein isolate and hydroxypropylmethylcellulose (HPMC)). The emulsion digestion was carried out in two continuous stages at 37 °C: 1) under simulated gastric conditions (1 h) using pepsin and phosphatidylcholine (simulated gastric fluid: pH 2.5, NaCl, NaH<inf>2</inf>PO<inf>4</inf>, KCl and CaCl<inf>2</inf>) and 2) under simulated intestinal conditions (1 h) with bile salts, pancreatic lipase, trypsin and chymotrypsin (simulated intestinal fluid: pH 7.0, K<inf>2</inf>HPO<inf>4</inf>, NaCl and CaCl<inf>2</inf>). The changes in the particle size distributions, the interfacial area and their microstructures were analyzed as a function of the digestion time. The free fatty acid release during the simulated intestinal stage was also determined and an empirical model was fitted to estimate different kinetic parameters. Irrespective of the composition/structure of emulsions, the initial surface area was found to determine the initial rate of lipolysis. Soy protein was the protein that forms the most resistant emulsion to digestion, showing a degree of free fatty acid release similar to HPMC, which is a non digestible emulsifier. The results are discussed on the basis of the role of bile salts and its effect on oil/water interfaces. © 2015 Elsevier Ltd.
format JOUR
author Bellesi, F.A.
Martinez, M.J.
Pizones Ruiz-Henestrosa, V.M.
Pilosof, A.M.R.
author_facet Bellesi, F.A.
Martinez, M.J.
Pizones Ruiz-Henestrosa, V.M.
Pilosof, A.M.R.
author_sort Bellesi, F.A.
title Comparative behavior of protein or polysaccharide stabilized emulsion under in vitro gastrointestinal conditions
title_short Comparative behavior of protein or polysaccharide stabilized emulsion under in vitro gastrointestinal conditions
title_full Comparative behavior of protein or polysaccharide stabilized emulsion under in vitro gastrointestinal conditions
title_fullStr Comparative behavior of protein or polysaccharide stabilized emulsion under in vitro gastrointestinal conditions
title_full_unstemmed Comparative behavior of protein or polysaccharide stabilized emulsion under in vitro gastrointestinal conditions
title_sort comparative behavior of protein or polysaccharide stabilized emulsion under in vitro gastrointestinal conditions
url http://hdl.handle.net/20.500.12110/paper_0268005X_v52_n_p47_Bellesi
work_keys_str_mv AT bellesifa comparativebehaviorofproteinorpolysaccharidestabilizedemulsionunderinvitrogastrointestinalconditions
AT martinezmj comparativebehaviorofproteinorpolysaccharidestabilizedemulsionunderinvitrogastrointestinalconditions
AT pizonesruizhenestrosavm comparativebehaviorofproteinorpolysaccharidestabilizedemulsionunderinvitrogastrointestinalconditions
AT pilosofamr comparativebehaviorofproteinorpolysaccharidestabilizedemulsionunderinvitrogastrointestinalconditions
_version_ 1807323413302214656