Demonstrates effective surface functionalization in hydrogels, indicating improved biointerface properties.
High Resolution Image Download MS PowerPoint Slide Advances in hydrogel research have enabled the design of bulk networks with diverse functionalities; however, precise control of interfacial properties remains a key challenge to expanding their applications, particularly in biointerfaces. Here, we report a simple and versatile surface functionalization strategy based on the self-assembly of terminally modified cello-oligosaccharides. When azido-functionalized cello-oligosaccharides dissolved in 85% phosphoric acid are applied to hydrogel surfaces, mixing with the intrinsic water within the hydrogels induces rapid self-assembly, forming nanostructured granular coatings at the interface. This method is applicable to both chemically and physically cross-linked hydrogels. The resulting azido-functionalized surfaces enable postfunctionalization via click chemistry, allowing biomolecule immobilization. As a proof of concept, antigen-conjugated hydrogels were used for the detection of specific immunoglobulin G, exhibiting selective responses even in serum-containing environments due to the antibiofouling properties of the assemblies. These findings establish terminally modified cello-oligosaccharides as a new class of interfacial modifiers for hydrogels, providing a facile route to biofunctional and antifouling interfaces for sensing and diagnostic applications.
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Sentosa et al. (2026) studied this question.
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