“…an exopolysaccharide produced by some non-pathogenic bacteria, namely the acetic acid bacteria of the genus Komagataeibacter (formerly classified as Gluconacetobacter) [17,18], is gaining increasing attention in the biomedical realm [19][20][21], particularly as a wound-dressing material [19,22,23]. Hence, the current study was inspired not only by the biocompatibility, high water-retention capacity, nanostructured porous network and good in vivo skin compatibility of BNC [20,24], but also by the fact that this exopolysaccharide can be directly produced in the form of membranes or films with customizable size and shape, and can house an array of active molecules (e.g., lidocaine [25,26], diclofenac [27,28], amoxicillin [29] and levofloxacin [30]) and macromolecules (e.g., poly([2-(methacryloyloxy)ethyl]trimethylammonium chloride) [31] and vitamin B-based ionic liquids [32]) that confer new functionalities to the ensuing materials. Although (i) HA has already been added to the culture media during BNC biosynthesis, to obtain BNC/HA membranes with no specific application [33], and (ii) the combination between BNC and DCF has already been studied for transdermal delivery [27], the coalition of BNC with HA and DCF has not yet been studied, at least to the best of our knowledge, for the potential treatment of aphthous stomatitis.…”