Supramolecular hybrid hydrogels as rapidly on-demand dissoluble, self-healing, and biocompatible burn dressings

Despite decades of efforts, state-of-the-art synthetic burn dressings to treat partial-thickness burns are still far from ideal. Current dressings adhere to the wound and necessitate debridement. This work describes the first supramolecular hybrid hydrogel (SHH) burn dressing that is biocompatible, self-healable, and on-demand dissoluble for easy and trauma-free removal, prepared by a simple, fast, and scalable method. These SHHs leverage the interactions of a custom-designed cationic copolymer via host-guest chemistry with cucurbit[7]uril and electrostatic interactions with clay nanosheets coated with an anionic polymer to achieve enhanced me-chanical properties and fast on-demand dissolution. The SHHs show high mechanical strength (>50 kPa), self -heal rapidly in-1 min, and dissolve quickly (4-6 min) using an amantadine hydrochloride (AH) solution that breaks the supramolecular interactions in the SHHs. Neither the SHHs nor the AH solution has any adverse effects on human dermal fibroblasts or epidermal keratinocytes in vitro. The SHHs also do not elicit any significant cytokine response in vitro. Furthermore, in vivo murine experiments show no immune or inflammatory cell infiltration in the subcutaneous tissue and no change in circulatory cytokines compared to sham controls. Thus, these SHHs present excellent burn dressing candidates to reduce the time of pain and time associated with dressing changes.

Automated summary

This study developed a novel biocompatible, self-healable, and on-demand dissoluble supramolecular hybrid hydrogel burn dressing. By leveraging the interactions of a custom-designed cationic copolymer with cucurbit[7]uril and electrostatic interactions with clay nanosheets coated with an anionic polymer, the dressing achieved enhanced mechanical properties and fast on-demand dissolution. The dressing showed high mechanical strength (>50 kPa), rapid self-healing (within 1 minute), and quick dissolution (4-6 minutes) using an amantadine hydrochloride solution. It did not have any adverse effects on human dermal fibroblasts or epidermal keratinocytes in vitro and did not elicit any immune or inflammatory response in vivo murine experiments.