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Correlating Digestion-Driven Self-Assembly in Milk and Infant Formulas with Changes in Lipid Composition

[Image: see text] Lipids in mammalian milks such as bovine milk and human breast milk have been shown to self-assemble into various liquid crystalline materials during digestion. In this study, the direct correlation between the composition of the lipids from three types of mammalian milk, three bra...

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Autores principales: Pham, Anna C., Peng, Kang-Yu, Salim, Malinda, Ramirez, Gisela, Hawley, Adrian, Clulow, Andrew J., Boyd, Ben J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241073/
https://www.ncbi.nlm.nih.gov/pubmed/32455340
http://dx.doi.org/10.1021/acsabm.0c00131
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author Pham, Anna C.
Peng, Kang-Yu
Salim, Malinda
Ramirez, Gisela
Hawley, Adrian
Clulow, Andrew J.
Boyd, Ben J.
author_facet Pham, Anna C.
Peng, Kang-Yu
Salim, Malinda
Ramirez, Gisela
Hawley, Adrian
Clulow, Andrew J.
Boyd, Ben J.
author_sort Pham, Anna C.
collection PubMed
description [Image: see text] Lipids in mammalian milks such as bovine milk and human breast milk have been shown to self-assemble into various liquid crystalline materials during digestion. In this study, the direct correlation between the composition of the lipids from three types of mammalian milk, three brands of infant formulas (IFs), and soy milk and the liquid crystalline structures that form during their digestion was investigated to link the material properties to the composition. The self-assembly behavior was assessed using in vitro digestion coupled with in situ small-angle X-ray scattering (SAXS). Lipid composition was determined during in vitro digestion using ex situ liquid chromatography–mass spectrometry. All tested milks self-assembled into ordered structures during digestion, with the majority of milks displaying nonlamellar phases. Milks that released mostly long-chain fatty acids (>95 mol % of the top 10 fatty acids released) with more than 47 mol % unsaturation predominantly formed a micellar cubic phase during digestion. Other milks released relatively more medium-chain fatty acids and medium-chain monoglycerides and produced a range of ordered liquid crystalline structures including the micellar cubic phase, the hexagonal phase, and the bicontinuous cubic phase. One infant formula did not form liquid crystalline structures at all as a consequence of differences in fatty acid distributions. The self-assembly phenomenon provides a powerful discriminator between different classes of nutrition and a roadmap for the design of human milklike systems and is anticipated to have important implications for nutrient transport and the delivery of bioactives.
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spelling pubmed-72410732020-05-21 Correlating Digestion-Driven Self-Assembly in Milk and Infant Formulas with Changes in Lipid Composition Pham, Anna C. Peng, Kang-Yu Salim, Malinda Ramirez, Gisela Hawley, Adrian Clulow, Andrew J. Boyd, Ben J. ACS Appl Bio Mater [Image: see text] Lipids in mammalian milks such as bovine milk and human breast milk have been shown to self-assemble into various liquid crystalline materials during digestion. In this study, the direct correlation between the composition of the lipids from three types of mammalian milk, three brands of infant formulas (IFs), and soy milk and the liquid crystalline structures that form during their digestion was investigated to link the material properties to the composition. The self-assembly behavior was assessed using in vitro digestion coupled with in situ small-angle X-ray scattering (SAXS). Lipid composition was determined during in vitro digestion using ex situ liquid chromatography–mass spectrometry. All tested milks self-assembled into ordered structures during digestion, with the majority of milks displaying nonlamellar phases. Milks that released mostly long-chain fatty acids (>95 mol % of the top 10 fatty acids released) with more than 47 mol % unsaturation predominantly formed a micellar cubic phase during digestion. Other milks released relatively more medium-chain fatty acids and medium-chain monoglycerides and produced a range of ordered liquid crystalline structures including the micellar cubic phase, the hexagonal phase, and the bicontinuous cubic phase. One infant formula did not form liquid crystalline structures at all as a consequence of differences in fatty acid distributions. The self-assembly phenomenon provides a powerful discriminator between different classes of nutrition and a roadmap for the design of human milklike systems and is anticipated to have important implications for nutrient transport and the delivery of bioactives. American Chemical Society 2020-05-04 2020-05-18 /pmc/articles/PMC7241073/ /pubmed/32455340 http://dx.doi.org/10.1021/acsabm.0c00131 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Pham, Anna C.
Peng, Kang-Yu
Salim, Malinda
Ramirez, Gisela
Hawley, Adrian
Clulow, Andrew J.
Boyd, Ben J.
Correlating Digestion-Driven Self-Assembly in Milk and Infant Formulas with Changes in Lipid Composition
title Correlating Digestion-Driven Self-Assembly in Milk and Infant Formulas with Changes in Lipid Composition
title_full Correlating Digestion-Driven Self-Assembly in Milk and Infant Formulas with Changes in Lipid Composition
title_fullStr Correlating Digestion-Driven Self-Assembly in Milk and Infant Formulas with Changes in Lipid Composition
title_full_unstemmed Correlating Digestion-Driven Self-Assembly in Milk and Infant Formulas with Changes in Lipid Composition
title_short Correlating Digestion-Driven Self-Assembly in Milk and Infant Formulas with Changes in Lipid Composition
title_sort correlating digestion-driven self-assembly in milk and infant formulas with changes in lipid composition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241073/
https://www.ncbi.nlm.nih.gov/pubmed/32455340
http://dx.doi.org/10.1021/acsabm.0c00131
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