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Microencapsulation of rice bran oil using pea protein and maltodextrin mixtures as wall material

In this work, the encapsulation of rice bran oil extracted using supercritical CO(2) has been studied. In the first stage, the emulsification process by high pressure homogenization was studied and optimized. The effect of the working pressure (60–150 MPa), the composition of the carrier (mixtures o...

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Autores principales: Benito-Román, Ó., Sanz, T., Beltrán, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118307/
https://www.ncbi.nlm.nih.gov/pubmed/32258508
http://dx.doi.org/10.1016/j.heliyon.2020.e03615
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author Benito-Román, Ó.
Sanz, T.
Beltrán, S.
author_facet Benito-Román, Ó.
Sanz, T.
Beltrán, S.
author_sort Benito-Román, Ó.
collection PubMed
description In this work, the encapsulation of rice bran oil extracted using supercritical CO(2) has been studied. In the first stage, the emulsification process by high pressure homogenization was studied and optimized. The effect of the working pressure (60–150 MPa), the composition of the carrier (mixtures of pea protein isolate (PPI) and maltodextrin (MD), from 50 to 90% of PPI) and the carrier to oil ratio (2–4) on the emulsion droplet size (EDS) was studied. To minimize the EDS, moderate pressures (114 MPa), a carrier composed mainly by PPI (64%) and carrier to oil ratios around 3.2 were required. The emulsion obtained in the optimal conditions (EDS = 189 ± 3nm) was dried using different technologies (spray-drying, PGSS-drying and freeze drying). The supercritical CO(2) based drying process (PGSS) provided spherical particles that resulted in the smallest average size (but broader distribution) and lower encapsulation efficiency (53 ± 2%).
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spelling pubmed-71183072020-04-06 Microencapsulation of rice bran oil using pea protein and maltodextrin mixtures as wall material Benito-Román, Ó. Sanz, T. Beltrán, S. Heliyon Article In this work, the encapsulation of rice bran oil extracted using supercritical CO(2) has been studied. In the first stage, the emulsification process by high pressure homogenization was studied and optimized. The effect of the working pressure (60–150 MPa), the composition of the carrier (mixtures of pea protein isolate (PPI) and maltodextrin (MD), from 50 to 90% of PPI) and the carrier to oil ratio (2–4) on the emulsion droplet size (EDS) was studied. To minimize the EDS, moderate pressures (114 MPa), a carrier composed mainly by PPI (64%) and carrier to oil ratios around 3.2 were required. The emulsion obtained in the optimal conditions (EDS = 189 ± 3nm) was dried using different technologies (spray-drying, PGSS-drying and freeze drying). The supercritical CO(2) based drying process (PGSS) provided spherical particles that resulted in the smallest average size (but broader distribution) and lower encapsulation efficiency (53 ± 2%). Elsevier 2020-04-01 /pmc/articles/PMC7118307/ /pubmed/32258508 http://dx.doi.org/10.1016/j.heliyon.2020.e03615 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Benito-Román, Ó.
Sanz, T.
Beltrán, S.
Microencapsulation of rice bran oil using pea protein and maltodextrin mixtures as wall material
title Microencapsulation of rice bran oil using pea protein and maltodextrin mixtures as wall material
title_full Microencapsulation of rice bran oil using pea protein and maltodextrin mixtures as wall material
title_fullStr Microencapsulation of rice bran oil using pea protein and maltodextrin mixtures as wall material
title_full_unstemmed Microencapsulation of rice bran oil using pea protein and maltodextrin mixtures as wall material
title_short Microencapsulation of rice bran oil using pea protein and maltodextrin mixtures as wall material
title_sort microencapsulation of rice bran oil using pea protein and maltodextrin mixtures as wall material
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118307/
https://www.ncbi.nlm.nih.gov/pubmed/32258508
http://dx.doi.org/10.1016/j.heliyon.2020.e03615
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