Stimuli-responsive graphene-based hydrogel driven by disruption of triazine hydrophobic interactions.

The study reported here concerns the preparation of a novel graphene-diaminotriazine (G-DAT) nanocomposite hydrogel for application in the drug delivery field. The hybrid nature of this material is founded on two key elements: the presence of the DAT backbone induced the formation of hydrophobic regions that allowed efficient loading of a series of drugs of increasing hydrophobicity (Metronidazole, Benzocaine, Ibuprofen, Naproxen and Imipramine), while simultaneously endowing swelling-induced pH-responsiveness to the hydrogel. Additionally, the incorporation of graphene was found to interfere with these hydrophobic domains through favourable non-covalent interactions, thus leading to the partial disruption of these aggregates. As a consequence, graphene facilitated and enhanced the release of model hydrophobic drug Imipramine in a synergistic manner with the pH trigger, and increased the swelling capacities and improved mechanical performance. This hybrid hydrogel can therefore be envisaged as a proof-of-concept system for the release of hydrophobic compounds in the field of drug delivery.

Physically Cross-Linked Hydrogel Based on Phenyl-1,3,5-triazine: Soft Scaffold with Aggregation-Induced Emission.

A phenyltriazine compound has been used for the first time as a monomer in the construction of a hydrogel. This physically cross-linked soft material showed blue fluorescence when excited under UV-light. Polymer formation and intermolecular H-bonds arising from triazine moieties operate as aggregation-induced emission (AIE) mechanisms. The combination of soft materials and AIE properties expands the applications of these materials. As a proof of concept, two luminescent dyes have been incorporated into the hydrogel to produce a white-light-emitting material.