Hydrogen sulfide (H₂S) is increasingly recognized as a key endogenous gasotransmitter involved in tissue repair, angiogenesis, inflammation modulation, and cytoprotection. Its biological activity, mediated through enzymatic pathways including cystathionine-β-synthase (CBS), cystathionine-γ-lyase (CSE), and 3-mercapto-pyruvate sulfurtransferase (3-MST), supports the therapeutic rationale for exogenous H₂S supplementation in impaired wound healing. Sulphurous thermal spring waters represent a traditional yet biologically relevant source of H₂S exposure, particularly in dermatological and chronic wound conditions. However, the clinical translation of H₂S therapy is limited by the molecule’s volatility and rapid degradation. Nano-engineered delivery systems have recently emerged as promising tools to enable controlled and sustained H₂S release at the wound site.
Hydrogen sulfide for nano-engineered gas transmitter releasing dressings in wound healing: translational / Crucianelli, S., Mariano, A., Moretti, F., Barile, D., Korraqe, A., Scotto D'Abusco, A., D'Erasmo, L., Durante, C., Fontana, M.. - (2026), pp. 422-422. (WUWHS 2026. World union of wound healing societies. Global paradigm shift: wound care specialty & recognition Kuala Lumpur, Malaysia ).
Hydrogen sulfide for nano-engineered gas transmitter releasing dressings in wound healing: translational
Serena Crucianelli
;Alessia Mariano;Ferdinando Moretti;Denise Barile;Alma Korraqe;Anna Scotto d'Abusco;Laura d'Erasmo;Cosimo Durante;Mario Fontana
2026
Abstract
Hydrogen sulfide (H₂S) is increasingly recognized as a key endogenous gasotransmitter involved in tissue repair, angiogenesis, inflammation modulation, and cytoprotection. Its biological activity, mediated through enzymatic pathways including cystathionine-β-synthase (CBS), cystathionine-γ-lyase (CSE), and 3-mercapto-pyruvate sulfurtransferase (3-MST), supports the therapeutic rationale for exogenous H₂S supplementation in impaired wound healing. Sulphurous thermal spring waters represent a traditional yet biologically relevant source of H₂S exposure, particularly in dermatological and chronic wound conditions. However, the clinical translation of H₂S therapy is limited by the molecule’s volatility and rapid degradation. Nano-engineered delivery systems have recently emerged as promising tools to enable controlled and sustained H₂S release at the wound site.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


