| Literature DB >> 32503293 |
Maddalena Sguizzato1, Paolo Mariani2, Francesco Spinozzi2, Mascia Benedusi3, Franco Cervellati3, Rita Cortesi1, Markus Drechsler4, Roxane Prieux3, Giuseppe Valacchi3,5,6, Elisabetta Esposito1.
Abstract
Ethosome represents a smart transdermal vehicle suitable for solubilization and cutaneous application of drugs. Coenzyme Q10 is an endogenous antioxidant whose supplementation can counteract many cutaneous disorders and pathologies. In this respect, the present study describes the production, characterization, and cutaneous protection of phosphatidylcholine based ethosomes as percutaneous delivery systems for coenzyme Q10. CoQ10 entrapment capacity in ethosomes was almost 100%, vesicles showed the typical 'fingerprint' structure, while mean diameters were around 270 nm, undergoing an 8% increase after 3 months from production. An ex-vivo study, conducted by transmission electron microscopy, could detect the uptake of ethosomes in human skin fibroblasts and the passage of the vesicles through 3D reconstituted human epidermis. Immunofluorescence analyses were carried on both on fibroblasts and 3D reconstituted human epidermis treated with ethosomes in the presence of H2O2 as oxidative stress challenger, evaluating 4-hydroxynonenal protein adducts which is as a reliable biomarker for oxidative damage. Notably, the pretreatment with CoQ10 loaded in ethosomes exerted a consistent protective effect against oxidative stress, in both models, fibroblasts and in reconstituted human epidermis respectively.Entities:
Keywords: H2O2; dermal administration; ethosome; penetration enhancers; reconstituted human epidermis; small angle X-ray scattering; ubiquinone
Year: 2020 PMID: 32503293 DOI: 10.3390/antiox9060485
Source DB: PubMed Journal: Antioxidants (Basel) ISSN: 2076-3921