Acmella oleracea and Zingiber officinale (ginger) are two plants of great interest due to their antioxidant, antimicrobial, and especially anti-inflammatory properties. These effects are mainly attributed to the presence of bioactive compounds such as spilanthol in Acmella oleracea and [6]-gingerol in Zingiber officinale. However, [6]-gingerol is primarily metabolized at the gastrointestinal and hepatic levels after oral administration, limiting its systemic bioavailability and effectiveness. In this study, a cream formulation containing both extracts was prepared using a preformed commercial transdermal vehicle and characterised through rheological studies. The ex vivo skin permeation of spilanthol and [6]-gingerol was evaluated using Franz diffusion cells. Results showed that the presence of Acmella oleracea lipophilic extract promoted the permeation of [6]-gingerol. Moreover, no histological alterations were observed in explanted human skin after transdermal application in a fluidic dynamic system. Based on these findings, topical administration of a formulation containing both Zingiber officinale and Acmella oleracea lipophilic extracts appears to be a promising strategy for enhancing the skin permeability of the active ingredients and, specifically for [6]-gingerol, avoiding its transformation in the gastrointestinal tract.

Enhanced transdermal delivery of [6]-Gingerol via Co-Administration of Acmella oleracea and Zingiber officinale lipophilic extracts

Magnano, Greta Camilla
Primo
Writing – Original Draft Preparation
;
Glerean, Martina
Secondo
Membro del Collaboration Group
;
Abrami, Michela
Formal Analysis
;
Larese Filon, Francesca
Funding Acquisition
;
Voinovich, Dario
Penultimo
Conceptualization
;
Hasa, Dritan
Ultimo
Writing – Review & Editing
2026-01-01

Abstract

Acmella oleracea and Zingiber officinale (ginger) are two plants of great interest due to their antioxidant, antimicrobial, and especially anti-inflammatory properties. These effects are mainly attributed to the presence of bioactive compounds such as spilanthol in Acmella oleracea and [6]-gingerol in Zingiber officinale. However, [6]-gingerol is primarily metabolized at the gastrointestinal and hepatic levels after oral administration, limiting its systemic bioavailability and effectiveness. In this study, a cream formulation containing both extracts was prepared using a preformed commercial transdermal vehicle and characterised through rheological studies. The ex vivo skin permeation of spilanthol and [6]-gingerol was evaluated using Franz diffusion cells. Results showed that the presence of Acmella oleracea lipophilic extract promoted the permeation of [6]-gingerol. Moreover, no histological alterations were observed in explanted human skin after transdermal application in a fluidic dynamic system. Based on these findings, topical administration of a formulation containing both Zingiber officinale and Acmella oleracea lipophilic extracts appears to be a promising strategy for enhancing the skin permeability of the active ingredients and, specifically for [6]-gingerol, avoiding its transformation in the gastrointestinal tract.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/3128300
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