Nanocellulose with Dual Carboxy and Aldehyde Functionality: a Modular Platform for Hydrogel Formation and Sustained Drug Release

Abstract

Nanocellulose-based hydrogels hold great promise for biomedical applications, particularly as localized drug delivery systems, due to their biocompatibility, tuneable porosity, and soft-tissue mimicking properties. However, most reported systems rely on single-mode crosslinking strategies and exhibit rapid burst release, limiting sustained therapeutic delivery.Herein, we report the synthesis and full characterization of a novel bifunctional crystalline nanocellulose bearing both carboxy and dialdehyde groups. This dual-functionalization was achieved via a sequential 2,2,6,6-tetramethylpiperidin-1yl)oxidanyl (TEMPO)-mediated oxidation followed by sodium periodate treatment, enabling reactivity with diamine-based crosslinkers. Hydrogels were prepared using either spermine or ε-poly-L-lysine through electrostatic or covalent crosslinking.The resulting materials exhibited tunable rheological properties, homogeneous and porous structures, and high in vitro biocompatibility. As a proof-of-concept, the chemotherapeutic agent doxorubicin was incorporated into selected hydrogel formulations, showing a sustained release over three weeks without burst effect. These findings highlight the potential of bifunctional CNCs as a modular and customizable platform for the development of injectable hydrogels for prolonged local drug delivery.