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Impact of pasteurization on the self-assembly of human milk lipids during digestion
Human milk is critical for the survival and development of infants. This source of nutrition contains components that protect against infections while stimulating immune maturation. In cases where the mother's own milk is unavailable, pasteurized donor milk is the preferred option. Although pas...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065913/ https://www.ncbi.nlm.nih.gov/pubmed/35181315 http://dx.doi.org/10.1016/j.jlr.2022.100183 |
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author | Binte Abu Bakar, Syaza Y. Salim, Malinda Clulow, Andrew J. Hawley, Adrian Pelle, Joseph Geddes, Donna T. Nicholas, Kevin R. Boyd, Ben J. |
author_facet | Binte Abu Bakar, Syaza Y. Salim, Malinda Clulow, Andrew J. Hawley, Adrian Pelle, Joseph Geddes, Donna T. Nicholas, Kevin R. Boyd, Ben J. |
author_sort | Binte Abu Bakar, Syaza Y. |
collection | PubMed |
description | Human milk is critical for the survival and development of infants. This source of nutrition contains components that protect against infections while stimulating immune maturation. In cases where the mother's own milk is unavailable, pasteurized donor milk is the preferred option. Although pasteurization has been shown to have minimal impact on the lipid and FA composition before digestion, no correlation has been made between the impact of pasteurization on the FFA composition and the self-assembly of lipids during digestion, which could act as delivery mechanisms for poorly water-soluble components. Pooled nonpasteurized and pasteurized human milk from a single donor was used in this study. The evolving FFA composition during digestion was determined using GC coupled to a flame ionization detector. In vitro digestion coupled to small-angle X-ray scattering was utilized to investigate the influence of different calcium levels, fat content, and the presence of bile salts on the extent of digestion and structural behavior of human milk lipids. Almost complete digestion was achieved when bile salts were added to the systems containing high calcium to milk fat ratio, with similar structural behavior of lipids during digestion of both types of human milk being apparent. In contrast, differences in the colloidal structures were formed during digestion in the absence of bile salt because of a greater amount of FFAs being released from the nonpasteurized than pasteurized milks. This difference in FFAs released from both types of human milk could result in varying nutritional implications for infants. |
format | Online Article Text |
id | pubmed-9065913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-90659132022-05-04 Impact of pasteurization on the self-assembly of human milk lipids during digestion Binte Abu Bakar, Syaza Y. Salim, Malinda Clulow, Andrew J. Hawley, Adrian Pelle, Joseph Geddes, Donna T. Nicholas, Kevin R. Boyd, Ben J. J Lipid Res Research Article Human milk is critical for the survival and development of infants. This source of nutrition contains components that protect against infections while stimulating immune maturation. In cases where the mother's own milk is unavailable, pasteurized donor milk is the preferred option. Although pasteurization has been shown to have minimal impact on the lipid and FA composition before digestion, no correlation has been made between the impact of pasteurization on the FFA composition and the self-assembly of lipids during digestion, which could act as delivery mechanisms for poorly water-soluble components. Pooled nonpasteurized and pasteurized human milk from a single donor was used in this study. The evolving FFA composition during digestion was determined using GC coupled to a flame ionization detector. In vitro digestion coupled to small-angle X-ray scattering was utilized to investigate the influence of different calcium levels, fat content, and the presence of bile salts on the extent of digestion and structural behavior of human milk lipids. Almost complete digestion was achieved when bile salts were added to the systems containing high calcium to milk fat ratio, with similar structural behavior of lipids during digestion of both types of human milk being apparent. In contrast, differences in the colloidal structures were formed during digestion in the absence of bile salt because of a greater amount of FFAs being released from the nonpasteurized than pasteurized milks. This difference in FFAs released from both types of human milk could result in varying nutritional implications for infants. American Society for Biochemistry and Molecular Biology 2022-02-16 /pmc/articles/PMC9065913/ /pubmed/35181315 http://dx.doi.org/10.1016/j.jlr.2022.100183 Text en © 2022 The Authors https://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 | Research Article Binte Abu Bakar, Syaza Y. Salim, Malinda Clulow, Andrew J. Hawley, Adrian Pelle, Joseph Geddes, Donna T. Nicholas, Kevin R. Boyd, Ben J. Impact of pasteurization on the self-assembly of human milk lipids during digestion |
title | Impact of pasteurization on the self-assembly of human milk lipids during digestion |
title_full | Impact of pasteurization on the self-assembly of human milk lipids during digestion |
title_fullStr | Impact of pasteurization on the self-assembly of human milk lipids during digestion |
title_full_unstemmed | Impact of pasteurization on the self-assembly of human milk lipids during digestion |
title_short | Impact of pasteurization on the self-assembly of human milk lipids during digestion |
title_sort | impact of pasteurization on the self-assembly of human milk lipids during digestion |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065913/ https://www.ncbi.nlm.nih.gov/pubmed/35181315 http://dx.doi.org/10.1016/j.jlr.2022.100183 |
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