Plasticizing properties of sugars and soluble dietary fibres revealed by high-throughput viscosity and time-domain 1H NMR relaxometry

Understanding and quantifying the plasticizing properties of soluble fibres (i.e. oligosaccharides, resistant dextrins and polydextrose) is essential for the rational design of sugar-reduced and fibre-enriched foods. This is challenging in complex polysaccharides systems. This study systematically investigated the relationships among viscosity, volumetric density of effective hydroxyl groups ( n OH,eff ), the ratio T g /T (with T g the glass transition temperature of the systems and T the actual temperature), and low-field NMR transverse relaxation time ( T 2 ) in aqueous solutions of sugars, polyols, soluble fibres, amino acids, and their mixtures. High-throughput viscosity measurements revealed that viscosity universally scaled with both n OH,eff and T g /T across all systems, collapsing data from structurally diverse plasticizers and multicomponent mixtures onto a single master curve. The log of T 2 relaxation times from time-domain 1 H NMR relaxometry exhibited strong linear correlations with n OH,eff and T g /T , demonstrating that molecular mobility and rheology are governed by hydrogen bond density when carbohydrate solutions are treated as a single effective solvent. By integrating viscosity and T 2 data within a Bayesian inference framework constrained by thermodynamic mixing rules, the dry T g of polydisperse soluble fibres was estimated with low uncertainty, overcoming limitations of conventional DSC-based approaches. This methodology provided a rapid, high-throughput strategy to quantify plasticizing properties and intrinsic material descriptors in complex carbohydrate systems. These insights support data-driven screening and design of polysaccharide-based ingredients with targeted textural functionality (e.g. sugar replacers), facilitating the development of healthier food formulations and valorization of carbohydrate-rich side-streams. • High-throughput viscosity and T 2 NMR revealed universal plasticization scaling laws • Viscosity is inversely related to the T 2 relaxation time for sugars and soluble fibres • Viscosity and T 2 relaxation scaled with hydrogen bond density and T g /T • A Bayesian framework enabled robust dry T g estimation in complex carbohydrates • Fast screening tool for sugar replacement and fibre-rich food design

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Publication Details

Journal
Food Hydrocolloids
Published
2026-04-16
DOI
https://doi.org/10.1016/j.foodhyd.2026.112780
Primary Topic
Food composition and properties
Type
article
Field-Weighted Citation Impact
0.00

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article

Plasticizing properties of sugars and soluble dietary fibres revealed by high-throughput viscosity and time-domain 1H NMR relaxometry

Stefano Renzetti, Lijiao Kan, Jolanda Henket, R.G.M. van der Sman
Food Hydrocolloids
Food composition and properties
article

Plasticizing properties of sugars and soluble dietary fibres revealed by high-throughput viscosity and time-domain 1H NMR relaxometry

Stefano Renzetti, Lijiao Kan, Jolanda Henket, R.G.M. van der Sman
article en

Abstract

Understanding and quantifying the plasticizing properties of soluble fibres (i.e. oligosaccharides, resistant dextrins and polydextrose) is essential for the rational design of sugar-reduced and fibre-enriched foods. This is challenging in complex polysaccharides systems. This study systematically investigated the relationships among viscosity, volumetric density of effective hydroxyl groups ( n OH,eff ), the ratio T g /T (with T g the glass transition temperature of the systems and T the actual temperature), and low-field NMR transverse relaxation time ( T 2 ) in aqueous solutions of sugars, polyols, soluble fibres, amino acids, and their mixtures. High-throughput viscosity measurements revealed that viscosity universally scaled with both n OH,eff and T g /T across all systems, collapsing data from structurally diverse plasticizers and multicomponent mixtures onto a single master curve. The log of T 2 relaxation times from time-domain 1 H NMR relaxometry exhibited strong linear correlations with n OH,eff and T g /T , demonstrating that molecular mobility and rheology are governed by hydrogen bond density when carbohydrate solutions are treated as a single effective solvent. By integrating viscosity and T 2 data within a Bayesian inference framework constrained by thermodynamic mixing rules, the dry T g of polydisperse soluble fibres was estimated with low uncertainty, overcoming limitations of conventional DSC-based approaches. This methodology provided a rapid, high-throughput strategy to quantify plasticizing properties and intrinsic material descriptors in complex carbohydrate systems. These insights support data-driven screening and design of polysaccharide-based ingredients with targeted textural functionality (e.g. sugar replacers), facilitating the development of healthier food formulations and valorization of carbohydrate-rich side-streams. • High-throughput viscosity and T 2 NMR revealed universal plasticization scaling laws • Viscosity is inversely related to the T 2 relaxation time for sugars and soluble fibres • Viscosity and T 2 relaxation scaled with hydrogen bond density and T g /T • A Bayesian framework enabled robust dry T g estimation in complex carbohydrates • Fast screening tool for sugar replacement and fibre-rich food design

Food HydrocolloidsVol. 179
Wageningen University & Research (NL)
Top Sector Agri and Food
Zero hunger
Openalex Percentile: Top 16%
Food composition and properties
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