Multidrug Idebenone/Naproxen Co-loaded Aspasomes for Significant in vivo Anti-inflammatory Activity.

Nicola d'Avanzo, Maria Chiara Cristiano, Luisa Di Marzio, Maria Chiara Bruno, Donatella Paolino, Christian Celia, Massimo Fresta

Journal: ChemMedChem 2022;17(9):e202200067

PMID: 35194952

Abstract

The use of proper nanocarriers for dermal and transdermal delivery of anti-inflammatory drugs recently gained several attentions in the scientific community because they pass intact and accumulate payloads in the deepest layers of skin tissue. Ascorbyl palmitate-based vesicles (aspasomes) can be considered a promising nanocarrier for dermal and transdermal delivery due to their skin whitening properties and suitable delivery of payloads through the skin. The aim of this study was the synthesis of multidrug Idebenone/naproxen co-loaded aspasomes for the development of an effective anti-inflammatory nanomedicine. Aspasomes had suitable physicochemical properties and were safe in vivo if topically applied on human healthy volunteers. Idebenone/naproxen co-loaded aspasomes demonstrated an increased therapeutic efficacy of payloads compared to the commercially available Naprosyn® gel, with a rapid decrease of chemical-induced erythema on human volunteers. These promising results strongly suggested a potential application of Idebenone/naproxen multidrug aspasomes for the development of an effective skin anti-inflammatory therapy.

© 2022 The Authors. ChemMedChem published by Wiley-VCH GmbH.

Address: Department of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Via dei Vestini n.31, 66100, Chieti, Italy.; Department of Experimental and Clinical Medicine, University "Magna Graecia" of Catanzaro Campus Universitario-Germaneto, Viale Europa, 88100, Catanzaro, Italy.; Department of Health Science, University "Magna Graecia" of Catanzaro Campus Universitario-Germaneto, Viale Europa, 88100, Catanzaro, Italy.

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