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Maria Manconi

Researcher at University of Cagliari

Publications -  170
Citations -  6693

Maria Manconi is an academic researcher from University of Cagliari. The author has contributed to research in topics: Vesicle & Liposome. The author has an hindex of 43, co-authored 147 publications receiving 5073 citations.

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Liposomes as carriers for dermal delivery of tretinoin: in vitro evaluation of drug permeation and vesicle-skin interaction.

TL;DR: Results showed that negatively charged liposomes strongly improved newborn pig skin hydration and TRA retention, though no evidence of intact vesicle penetration was found, and may be an interesting carrier for tretinoin in skin disease treatment, when appropriate formulations are used.
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Niosomes as carriers for tretinoin: III. A study into the in vitro cutaneous delivery of vesicle-incorporated tretinoin

TL;DR: Results showed that tretinoin cutaneous delivery is strongly affected by vesicle composition and thermodynamic activity of the drug, and small, negatively charged niosomal formulations, which are saturated with tretinin, have shown to give higher cutaneous drug retention than both liposomes and commercial formulation.
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Niosomes as carriers for tretinoin. I. Preparation and properties

TL;DR: Release data showed that tretinoin delivery is mainly affected by the vesicular structure and that tretsin delivery increased from MLVs to LUVs to SUVs.
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Liposomal incorporation of Artemisia arborescens L. essential oil and in vitro antiviral activity.

TL;DR: In this paper, the effect of liposomal inclusion on the in vitro antiherpetic activity of Artemisia arborescens L. essential oil was investigated, which showed that Artemisia essential oil can be incorporated in good amounts in the prepared vesicular dispersions.
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Development of curcumin loaded sodium hyaluronate immobilized vesicles (hyalurosomes) and their potential on skin inflammation and wound restoring.

TL;DR: In vivo tests underlined a good effectiveness of curcumin-loaded hyalurosomes to counteract 12-O-tetradecanoilphorbol (TPA)-produced inflammation and injuries, diminishing oedema formation, myeloperoxydase activity and providing an extensive skin reepithelization.