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      Microgelation imparts emulsifying ability to surface-inactive polysaccharides—bottom-up vs top-down approaches

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          Abstract

          In order to impart emulsifying ability to gel-forming polysaccharides that have not been used as emulsifying agents, three kinds of polysaccharides, agar, curdlan, and gellan gum were converted to microgels by different gelation methods via the bottom-up and top-down approaches. We clearly demonstrated that agar and curdlan acquired the ability to emulsify an edible oil by microgel formation. Among the colloidal properties of microgel suspensions such as microstructure, particle size, zeta-potential, viscosity, and surface hydrophobicity, we pointed out the importance of particle size on the emulsifying ability of polysaccharide-based microgels. The creaming behavior of the microgel-stabilized emulsions depended on the polysaccharide types and microgel preparation methods. The emulsion stability against oil droplet coalescence was extremely high for agar and curdlan microgel-stabilized emulsions during storage in the static condition, whereas different stability was observed for both the emulsions, that is, the curdlan microgel-based ones were more resistant to dynamic forcible destabilization by centrifugation than the agar ones, which can be attributed to the surface hydrophobicity of the microgels.

          Food Emulsion: Microgelation turns polysaccharides into emulsifying agents

          Polysaccharides are widely recognized as gelling agents while rarely used alone as emulsifying agents due to their surface inactiveness. Now Kentaro Matsumiya and coworkers from Kyoto University report the microgelated polysaccharide particles can emulsify soybean oil, forming so-called microgel-based Mickering emulsions. It was found that large microgels formed by agar and curdlan exhibited better emulsifying abilities compared to small gellan gum microgels, regardless of the preparation methods. The creaming behaviors varied with the changing polysaccharide types and microgel preparation methods. The static stability was quite high for all emulsions while their dynamic stability was different, which can be attributed to the surface hydrophobicity difference. It is noteworthy that the microgelation turned surface-inactive polysaccharides into effective emulsifying agents. The low-allergenic polysaccharide food emulsions might find usage practically soon.

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          Most cited references38

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          The development of microgels/nanogels for drug delivery applications

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            Polysaccharide hydrogels for modified release formulations.

            Hydrogels are three-dimensional, hydrophilic, polymeric networks, with chemical or physical cross-links, capable of imbibing large amounts of water or biological fluids. Among the numerous macromolecules that can be used for hydrogel formation, polysaccharides are extremely advantageous compared to synthetic polymers being widely present in living organisms and often being produced by recombinant DNA techniques. Coming from renewable sources, polysaccharides also have frequently economical advantages over synthetic polymers. Polysaccharides are usually non-toxic, biocompatible and show a number of peculiar physico-chemical properties that make them suitable for different applications in drug delivery systems. We review here a selection of the most important polysaccharides that have been studied and exploited in several fields related to pharmaceutics. Particular attention has been focused on the techniques used for the hydrogel network preparation, on the drug delivery results, on clinical applications as well as on the possible use of such systems as scaffolds for tissue engineering.
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              Emulsions stabilised by whey protein microgel particles: towards food-grade Pickering emulsions.

              We have investigated a new class of food-grade particles, whey protein microgels, as stabilisers of triglyceride-water emulsions. The sub-micron particles stabilized oil-in-water emulsions at all pH with and without salt. All emulsions creamed but exhibited exceptional resistance to coalescence. Clear correlations exist between the properties of the microgels in aqueous dispersion and the resulting emulsion characteristics. For conditions in which the particles were uncharged, fluid emulsions with relatively large drops were stabilised, whereas emulsions stabilized by charged particles contained smaller flocculated drops. A combination of optical microscopy of the drops and spectrophotometry of the resolved aqueous phase allowed us to estimate the interfacial adsorption densities of the particles using the phenomenon of limited coalescence. We deduce two classes of particle arrangement. Complete adsorption of the particles was obtained when they were neutral or when their charges were screened by salt resulting in at least one particle monolayer at the interface. By contrast, only around 50% of the particles adsorbed when they were charged with emulsion drops being covered by less than half a monolayer. These findings were supported by direct visualization of drop interfaces using cryo-scanning electron microscopy. Uncharged particles were highly aggregated and formed a continuous 2-D network at the interface. Otherwise particles organized as individual aggregates separated by particle-free regions. In this case, we suggest that some particles spread at the interface leading to the formation of a continuous protein membrane. Charged particles displayed the ability to bridge opposing interfaces of neighbouring drops to form dense particle disks protecting drops against coalescence; this is the main reason for the flocculation and stability of emulsions containing sparsely covered drops.
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                Author and article information

                Contributors
                +81-774-38-3748 , matsumiya.kentaro.l97@kyoto-u.jp , matumiya@kais.kyoto-u.ac.jp
                Journal
                NPJ Sci Food
                NPJ Sci Food
                NPJ Science of Food
                Nature Publishing Group UK (London )
                2396-8370
                20 August 2018
                20 August 2018
                2018
                : 2
                : 15
                Affiliations
                ISNI 0000 0004 0372 2033, GRID grid.258799.8, Laboratory of Quality Analysis and Assessment, Division of Agronomy and Horticultural Science, Graduate School of Agriculture, , Kyoto University, Gokasho, Uji, ; Kyoto, 611-0011 Japan
                Article
                23
                10.1038/s41538-018-0023-7
                6550241
                321aaaf8-1355-4eea-9e9c-8278da8bd2ee
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 1 February 2018
                : 8 July 2018
                : 18 July 2018
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100001691, Japan Society for the Promotion of Science (JSPS);
                Award ID: 16K07751
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2018

                colloids,biosurfaces,biopolymers,gels and hydrogels
                colloids, biosurfaces, biopolymers, gels and hydrogels

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