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June 5, 2026Small0 citationsOpen Access

Modular Molecular Design and Self‐Assembled Nanostructures of Saccharide‑Appended Cyclic Dipeptides for Glycosidase‑Responsive Supramolecular Hydrogels

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SSShintaro SugiuraRTRyuta TanakaSHSayuri L. Higashi

Key Points

  • This research aims to design saccharide-appended cyclic dipeptides for creating glycosidase-responsive supramolecular hydrogels.
  • Designed cyclic dipeptides with galactose and N-acetylneuraminic acid as building blocks.
  • Achieved β-galactosidase-responsive gel-to-sol and neuraminidase-responsive sol-to-gel transitions.
  • Employed aqueous self-assembly techniques under specific formulations.
  • Successfully transitioned from gel-to-sol using β-galactosidase applications.
  • Effectively transitioned from sol-to-gel using neuraminidase under optimal conditions.

Abstract

Glycosidase-responsive supramolecular hydrogels represent a promising class of soft materials for biomedical applications, as glycosidases play pivotal roles in various physiological processes and viral infections. In this study, saccharide-appended cyclic dipeptides are designed as modular building blocks for the construction of supramolecular hydrogel systems through aqueous self-assembly. Notably, β-galactosidase-responsive gel-to-sol and neuraminidase (sialidase)-responsive sol-to-gel transitions are achieved by employing cyclic dipeptides appended with galactose and N-acetylneuraminic acid, respectively, under appropriate formulations.

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Cite This Study

Sugiura et al. (2026) studied this question.

synapsesocial.com/papers/6a22698b763171746d5481aehttps://doi.org/10.1002/smll.73943
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