4.7 Article

Design and in vitro effectiveness evaluation of Echium amoenum extract loaded in bioadhesive phospholipid vesicles tailored for mucosal delivery

Journal

INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 634, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ijpharm.2023.122650

Keywords

Plant extract; Liposomes; Mucin; Xanthan gum; Carboxymethyl cellulose; Keratinocytes; Viscosity; Mucoadhesion; Scratch assay

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In this study, an antioxidant phytocomplex was extracted from the flowers of E. amoenum and loaded into liposomes. The liposomes were enriched with different bioadhesive polymers individually or in combination. The physico-chemical properties of the prepared vesicles were measured, as well as their stability on storage. The biocompatibility and the ability of the formulations to protect keratinocytes and promote cell migration were evaluated in vitro.
The Echium amoenum Fisch. and C.A. Mey. (E. amoenum) is an herb native from Iranian shrub, and its blue-violet flowers are traditionally used as medical plants. In the present study, an antioxidant phytocomplex was extracted from the flowers of E. amoenum by ultrasounds-assisted hydroalcoholic maceration. The main components, contained in the extract, have been detected using HPLC-DAD, and rosmarinic acid was found to be the most abundant. The antioxidant power of the extract along with the phenolic content were measured using colorimetric assays. The extract was loaded in liposomes, which were enriched adding different bioadhesive polymers (i.e., mucin, xanthan gum and carboxymethyl cellulose sodium salt) individually or in combination. The main physico-chemical properties (i.e. size, size distribution, surface charge) of the prepared vesicles were measured as well as their stability on storage. The viscosity of dispersion and the ability of vesicles to interact with mucus were evaluated measuring their stability in a mucin dispersion and mobility in a mucin film. The biocompatibility and the ability of the formulations to protect keratinocytes from damages caused by hydrogen peroxide and to promote the cell migration were measured in vitro.

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