Quantification of food polysaccharide mixtures by 1 H NMR
Polysaccharides are food ingredients that critically determine rheological properties and shelf life. A qualitative and quantitative assessment on food-specific polysaccharide mixtures by H NMR is presented. The method is based on the identification of intact polysaccharides, combined with a quantit...
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Veröffentlicht in: | Carbohydrate polymers 2018-01, Vol.179, p.379 |
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creator | Merkx, Donny W H Westphal, Yvonne van Velzen, Ewoud J J Thakoer, Kavish V de Roo, Niels van Duynhoven, John P M |
description | Polysaccharides are food ingredients that critically determine rheological properties and shelf life. A qualitative and quantitative assessment on food-specific polysaccharide mixtures by
H NMR is presented. The method is based on the identification of intact polysaccharides, combined with a quantitative analysis of their monosaccharide constituents. Identification of the polysaccharides is achieved by
H NMR line shape fitting with pure compound spectra. The monomeric composition was determined using the Saeman hydrolysis procedure, followed by direct monosaccharide quantification by
H NMR. In the quantification, both the monosaccharide degradation during hydrolysis, as well as a correction for the non-instantaneous polysaccharide dissolution were taken into account. These factors were particularly important for the quantification of pectins. The method showed overall good repeatability (RSD
=4.1±0.9%) and within-laboratory reproducibility (RSD
=6.1±1.4%) for various food polysaccharides. Polysaccharide mixtures were quantitatively resolved by a non-negative least squares estimation, using identified polysaccharides and their molar monosaccharide stoichiometry as prior knowledge. The accuracy and precision of the presented method make it applicable to a wide range of food polysaccharide mixtures with complex and overlapping
H NMR spectra. |
format | Article |
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H NMR is presented. The method is based on the identification of intact polysaccharides, combined with a quantitative analysis of their monosaccharide constituents. Identification of the polysaccharides is achieved by
H NMR line shape fitting with pure compound spectra. The monomeric composition was determined using the Saeman hydrolysis procedure, followed by direct monosaccharide quantification by
H NMR. In the quantification, both the monosaccharide degradation during hydrolysis, as well as a correction for the non-instantaneous polysaccharide dissolution were taken into account. These factors were particularly important for the quantification of pectins. The method showed overall good repeatability (RSD
=4.1±0.9%) and within-laboratory reproducibility (RSD
=6.1±1.4%) for various food polysaccharides. Polysaccharide mixtures were quantitatively resolved by a non-negative least squares estimation, using identified polysaccharides and their molar monosaccharide stoichiometry as prior knowledge. The accuracy and precision of the presented method make it applicable to a wide range of food polysaccharide mixtures with complex and overlapping
H NMR spectra.</description><identifier>EISSN: 1879-1344</identifier><identifier>PMID: 29111064</identifier><language>eng</language><publisher>England</publisher><subject>Dietary Carbohydrates - analysis ; Dietary Carbohydrates - isolation & purification ; Food Industry ; Hydrolysis ; Least-Squares Analysis ; Molecular Weight ; Monosaccharides - analysis ; Monosaccharides - chemistry ; Nuclear Magnetic Resonance, Biomolecular - methods ; Pectins - analysis ; Reproducibility of Results ; Water - chemistry</subject><ispartof>Carbohydrate polymers, 2018-01, Vol.179, p.379</ispartof><rights>Copyright © 2017 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29111064$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Merkx, Donny W H</creatorcontrib><creatorcontrib>Westphal, Yvonne</creatorcontrib><creatorcontrib>van Velzen, Ewoud J J</creatorcontrib><creatorcontrib>Thakoer, Kavish V</creatorcontrib><creatorcontrib>de Roo, Niels</creatorcontrib><creatorcontrib>van Duynhoven, John P M</creatorcontrib><title>Quantification of food polysaccharide mixtures by 1 H NMR</title><title>Carbohydrate polymers</title><addtitle>Carbohydr Polym</addtitle><description>Polysaccharides are food ingredients that critically determine rheological properties and shelf life. A qualitative and quantitative assessment on food-specific polysaccharide mixtures by
H NMR is presented. The method is based on the identification of intact polysaccharides, combined with a quantitative analysis of their monosaccharide constituents. Identification of the polysaccharides is achieved by
H NMR line shape fitting with pure compound spectra. The monomeric composition was determined using the Saeman hydrolysis procedure, followed by direct monosaccharide quantification by
H NMR. In the quantification, both the monosaccharide degradation during hydrolysis, as well as a correction for the non-instantaneous polysaccharide dissolution were taken into account. These factors were particularly important for the quantification of pectins. The method showed overall good repeatability (RSD
=4.1±0.9%) and within-laboratory reproducibility (RSD
=6.1±1.4%) for various food polysaccharides. Polysaccharide mixtures were quantitatively resolved by a non-negative least squares estimation, using identified polysaccharides and their molar monosaccharide stoichiometry as prior knowledge. The accuracy and precision of the presented method make it applicable to a wide range of food polysaccharide mixtures with complex and overlapping
H NMR spectra.</description><subject>Dietary Carbohydrates - analysis</subject><subject>Dietary Carbohydrates - isolation & purification</subject><subject>Food Industry</subject><subject>Hydrolysis</subject><subject>Least-Squares Analysis</subject><subject>Molecular Weight</subject><subject>Monosaccharides - analysis</subject><subject>Monosaccharides - chemistry</subject><subject>Nuclear Magnetic Resonance, Biomolecular - methods</subject><subject>Pectins - analysis</subject><subject>Reproducibility of Results</subject><subject>Water - chemistry</subject><issn>1879-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpjYuA0tDC31DU0NjHhYOAqLs4yAAIzQwN2Bg4jS0NDQwMzE04Gy8DSxLySzLTM5MSSzPw8hfw0hbT8_BSFgvycyuLE5OSMxKLMlFSF3MyKktKi1GKFpEoFQwUPBT_fIB4G1rTEnOJUXijNzSDn5hri7KFbUJqUm5oSX1CUmZtYVBkPs8uYoAIA7HQzFg</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Merkx, Donny W H</creator><creator>Westphal, Yvonne</creator><creator>van Velzen, Ewoud J J</creator><creator>Thakoer, Kavish V</creator><creator>de Roo, Niels</creator><creator>van Duynhoven, John P M</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20180101</creationdate><title>Quantification of food polysaccharide mixtures by 1 H NMR</title><author>Merkx, Donny W H ; Westphal, Yvonne ; van Velzen, Ewoud J J ; Thakoer, Kavish V ; de Roo, Niels ; van Duynhoven, John P M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_291110643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Dietary Carbohydrates - analysis</topic><topic>Dietary Carbohydrates - isolation & purification</topic><topic>Food Industry</topic><topic>Hydrolysis</topic><topic>Least-Squares Analysis</topic><topic>Molecular Weight</topic><topic>Monosaccharides - analysis</topic><topic>Monosaccharides - chemistry</topic><topic>Nuclear Magnetic Resonance, Biomolecular - methods</topic><topic>Pectins - analysis</topic><topic>Reproducibility of Results</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Merkx, Donny W H</creatorcontrib><creatorcontrib>Westphal, Yvonne</creatorcontrib><creatorcontrib>van Velzen, Ewoud J J</creatorcontrib><creatorcontrib>Thakoer, Kavish V</creatorcontrib><creatorcontrib>de Roo, Niels</creatorcontrib><creatorcontrib>van Duynhoven, John P M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Carbohydrate polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Merkx, Donny W H</au><au>Westphal, Yvonne</au><au>van Velzen, Ewoud J J</au><au>Thakoer, Kavish V</au><au>de Roo, Niels</au><au>van Duynhoven, John P M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantification of food polysaccharide mixtures by 1 H NMR</atitle><jtitle>Carbohydrate polymers</jtitle><addtitle>Carbohydr Polym</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>179</volume><spage>379</spage><pages>379-</pages><eissn>1879-1344</eissn><abstract>Polysaccharides are food ingredients that critically determine rheological properties and shelf life. A qualitative and quantitative assessment on food-specific polysaccharide mixtures by
H NMR is presented. The method is based on the identification of intact polysaccharides, combined with a quantitative analysis of their monosaccharide constituents. Identification of the polysaccharides is achieved by
H NMR line shape fitting with pure compound spectra. The monomeric composition was determined using the Saeman hydrolysis procedure, followed by direct monosaccharide quantification by
H NMR. In the quantification, both the monosaccharide degradation during hydrolysis, as well as a correction for the non-instantaneous polysaccharide dissolution were taken into account. These factors were particularly important for the quantification of pectins. The method showed overall good repeatability (RSD
=4.1±0.9%) and within-laboratory reproducibility (RSD
=6.1±1.4%) for various food polysaccharides. Polysaccharide mixtures were quantitatively resolved by a non-negative least squares estimation, using identified polysaccharides and their molar monosaccharide stoichiometry as prior knowledge. The accuracy and precision of the presented method make it applicable to a wide range of food polysaccharide mixtures with complex and overlapping
H NMR spectra.</abstract><cop>England</cop><pmid>29111064</pmid></addata></record> |
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source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Dietary Carbohydrates - analysis Dietary Carbohydrates - isolation & purification Food Industry Hydrolysis Least-Squares Analysis Molecular Weight Monosaccharides - analysis Monosaccharides - chemistry Nuclear Magnetic Resonance, Biomolecular - methods Pectins - analysis Reproducibility of Results Water - chemistry |
title | Quantification of food polysaccharide mixtures by 1 H NMR |
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