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      Divergent Deborah number-dependent transition from homogeneity to heterogeneity

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          Abstract

          Heterogeneous structures are ubiquitous in natural organisms. Native heterogeneous structures inspire many artificial structures that are playing important roles in modern society, while it is challenging to identify the relevant factors in forming these structures due to the complexity of living systems. Here, hybrid hydrogels consisting of flexible polymer networks with embedded stiff cellulose nanocrystals (CNCs) are considered an open system to simulate the generalized formation of heterogeneous core-sheath structures. As the result of the modified air drying process of hybrid hydrogels, the formation of heterogeneous core-sheath structure is found to be correlated to the relative evaporation speed. Specifically, the formation of such heterogeneity in xerogel fibers is found to be correlated with the divergence of Deborah number ( De). During the transition of De from large to small values with accompanying morphologies, the turning point is around De = 1. The mechanism can be considered a relative humidity-dependent glass transition behavior. These unique heterogeneous structures play a key role in tuning water permeation and water sorption capacity. Insights into these aspects can prospectively contribute to a better understanding of the native heterogeneous structures for bionics design.

          Abstract

          Due to the complexity of living systems, it is challenging to identify the factors influencing the formation of native heterogeneous structures. Here, the authors employ flexible polymer networks with embedded stiff cellulose nanocrystals to simulate heterogeneous core-sheath structures interrelated with the divergence of Deborah number.

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          Most cited references58

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          Pseudo-second order model for sorption processes

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            A reversible wet/dry adhesive inspired by mussels and geckos.

            The adhesive strategy of the gecko relies on foot pads composed of specialized keratinous foot-hairs called setae, which are subdivided into terminal spatulae of approximately 200 nm (ref. 1). Contact between the gecko foot and an opposing surface generates adhesive forces that are sufficient to allow the gecko to cling onto vertical and even inverted surfaces. Although strong, the adhesion is temporary, permitting rapid detachment and reattachment of the gecko foot during locomotion. Researchers have attempted to capture these properties of gecko adhesive in synthetic mimics with nanoscale surface features reminiscent of setae; however, maintenance of adhesive performance over many cycles has been elusive, and gecko adhesion is greatly diminished upon full immersion in water. Here we report a hybrid biologically inspired adhesive consisting of an array of nanofabricated polymer pillars coated with a thin layer of a synthetic polymer that mimics the wet adhesive proteins found in mussel holdfasts. Wet adhesion of the nanostructured polymer pillar arrays increased nearly 15-fold when coated with mussel-mimetic polymer. The system maintains its adhesive performance for over a thousand contact cycles in both dry and wet environments. This hybrid adhesive, which combines the salient design elements of both gecko and mussel adhesives, should be useful for reversible attachment to a variety of surfaces in any environment.
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              Hydrogels with tunable stress relaxation regulate stem cell fate and activity

              Natural extracellular matrices (ECMs) are viscoelastic and exhibit stress relaxation. However, hydrogels used as synthetic ECMs for three-dimensional (3D) culture are typically elastic. Here, we report a materials approach to tune the rate of stress relaxation of hydrogels for 3D culture, independently of the hydrogel’s initial elastic modulus, cell-adhesion-ligand density and degradation. We find that cell spreading, proliferation, and osteogenic differentiation of mesenchymal stem cells (MSCs) are all enhanced in cells cultured in gels with faster relaxation. Strikingly, MSCs form a mineralized, collagen-1-rich matrix similar to bone in rapidly relaxing hydrogels with an initial elastic modulus of 17 kPa. We also show that the effects of stress relaxation are mediated by adhesion-ligand binding, actomyosin contractility and mechanical clustering of adhesion ligands. Our findings highlight stress relaxation as a key characteristic of cell-ECM interactions and as an important design parameter of biomaterials for cell culture.
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                Author and article information

                Contributors
                kai.zhang@uni-goettingen.de
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                26 September 2023
                26 September 2023
                2023
                : 14
                : 6003
                Affiliations
                [1 ]Sustainable Materials and Chemistry, Department of Wood Technology and Wood-based Composites, University of Göttingen, ( https://ror.org/01y9bpm73) Büsgenweg 4, D-37077 Göttingen, Germany
                [2 ]Department of Wood Biology and Wood Products, University of Göttingen, ( https://ror.org/01y9bpm73) Büsgenweg 4, D-37077 Göttingen, Germany
                [3 ]Laboratory for Fluid Physics, Pattern Formation and Biocomplexity, Max Planck Institute for Dynamics and Self-Organization, ( https://ror.org/0087djs12) Am Faßberg 17, D-37077 Göttingen, Germany
                Author information
                http://orcid.org/0000-0001-5858-7535
                http://orcid.org/0000-0003-0778-4904
                http://orcid.org/0000-0002-2072-4722
                http://orcid.org/0000-0001-8518-6745
                http://orcid.org/0000-0002-5783-946X
                Article
                41738
                10.1038/s41467-023-41738-0
                10522598
                37752163
                ed64f4a4-e1ec-445d-822b-ca7f7e2b0cfd
                © Springer Nature Limited 2023

                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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 8 February 2023
                : 18 September 2023
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft (German Research Foundation);
                Award ID: INST186/1281-1/FUGG
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100011937, Niedersächsische Ministerium für Wissenschaft und Kultur (Lower Saxony Ministry of Science and Culture);
                Award ID: INST186/1281-1/FUGG
                Award Recipient :
                Categories
                Article
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                © Springer Nature Limited 2023

                Uncategorized
                gels and hydrogels,organic molecules in materials science
                Uncategorized
                gels and hydrogels, organic molecules in materials science

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