: Nanocellulose-based hydrogels hold great promise for biomedical applications, particularly as localized drug delivery systems, due to their biocompatibility, tunable 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-1-yl)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 a 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.

Nanocellulose with dual carboxy and aldehyde functionality: a modular platform for hydrogel formation and sustained drug release

Inzalaco G.;Chiariello M.;
2026

Abstract

: Nanocellulose-based hydrogels hold great promise for biomedical applications, particularly as localized drug delivery systems, due to their biocompatibility, tunable 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-1-yl)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 a 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.
2026
Istituto di Fisiologia Clinica - IFC - Sede Secondaria di Siena
Istituto degli Endotipi in Oncologia, Metabolismo e Immunologia "G. Salvatore" (IEOMI)
Glioblastoma
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/593601
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 0
  • ???jsp.display-item.citation.isi??? ND
social impact