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April 22, 2026Materials & Design0 citationsOpen Access

Cyclodextrin-Based deep eutectic Solvent-Constructed chitosan eutectogel for therapeutic delivery of Glabridin in diabetic wound management

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NZNanxiang ZhangHTHaoyun TanMXMingxin Xu

Key Points

  • This research aims to investigate the efficacy of a cyclodextrin-based eutectogel for drug delivery in diabetic wound management.
  • Developed a novel eutectogel using a cyclodextrin-based deep eutectic solvent and chitosan.
  • Conducted in vitro antibacterial assays against S. aureus and E. coli.
  • Evaluated wound healing efficacy in an infected diabetic wound model over 21 days.
  • Eutectogel showed over 99% antibacterial efficacy against tested bacteria.
  • Achieved a wound closure rate of 94.3% by day 21 in the diabetic wound model.
  • Enhanced healing mechanisms by scavenging reactive oxygen species and promoting macrophage polarization.

Abstract

• A novel adhesive eutectogel was developed by combining a cyclodextrin-based deep eutectic solvent with chitosan. • The deep eutectic solvent acts as both a solubilizer and a dynamic crosslinker, enabling sustained drug release over 10 days. • The eutectogel exhibited over 99% antibacterial efficacy by disrupting bacterial membrane integrity. • The gel promoted diabetic wound healing by scavenging reactive oxygen species, inhibiting the nuclear factor kappa-B pathway, and inducing macrophage polarization from the pro-inflammatory M1 to the reparative M2 phenotype. Diabetic wounds are hard to heal and prone to infection. Glabridin (GLD) can promote wound repair but suffers from poor solubility and photostability. This study developed an adhesive eutectogel (GLD/CS/DES) by combining a deep eutectic solvent (DES) formed from sulfobutyl ether-β-cyclodextrin and levulinic acid with chitosan (CS). The DES not only solubilizes GLD but also acts as a dynamic crosslinker, imparting favorable mechanical properties. The gel enabled sustained GLD release for over 10 days and effectively protected GLD from photodegradation. In vitro antibacterial assays demonstrated > 99% efficacy against S. aureus and E. coli by disrupting bacterial membrane integrity. In an infected diabetic wound model, the gel achieved a wound closure rate of 94.3% by day 21. Mechanistic studies revealed that the gel scavenged reactive oxygen species, inhibited the NF-κB pathway, and promoted macrophage polarization from the pro-inflammatory M1 to the reparative M2 phenotype, thereby ameliorating the immune microenvironment, enhancing angiogenesis, and accelerating tissue regeneration.

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Cite This Study

Zhang et al. (2026) studied this question.

synapsesocial.com/papers/69e864c46e0dea528dde96cehttps://doi.org/10.1016/j.matdes.2026.116047
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