Effect of liposomal formulation of ascorbic acid on corneal permeability.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
01 03 2023
Historique:
received: 19 08 2022
accepted: 02 02 2023
entrez: 1 3 2023
pubmed: 2 3 2023
medline: 4 3 2023
Statut: epublish

Résumé

Ascorbic acid (AA) has a pivotal role in corneal wound healing via stimulating the biosynthesis of highly organized extracellular matrix components, but its rapid degradation and low corneal permeability limits its therapeutic effects. In this paper, we present the pharmacokinetic properties of a liposomal-based formulation of AA in terms of corneal permeation. Chemical stability, shelf-life, and drug release rate of lyophilized liposome (AA-LLipo) formulation was determined in comparison to free-form of AA solution using high-performance liquid chromatography (HPLC) and rapid equilibrium dialysis. In vitro transcorneal permeability was studied using a parallel artificial membrane permeability assay (PAMPA). Ex vivo permeation was examined on AA-LLipo-treated porcine cornea by determining the AA content on the ocular surface, in the cornea as well as in the aqueous humor using HPLC, and by Raman-mapping visualizing the AA-distribution. Our results showed that the liposomal formulation improved the chemical stability of AA, while drug release was observed with the same kinetic efficiency as from the free-form of AA solution. Both corneal-PAMPA and porcine corneal permeability studies showed that AA-LLipo markedly improved the corneal absorption kinetics of AA, thus, increasing the AA content in the cornea and aqueous humor. AA-LLipo formulation could potentially increase the bioavailability of AA in corneal tissues.

Identifiants

pubmed: 36859418
doi: 10.1038/s41598-023-29290-9
pii: 10.1038/s41598-023-29290-9
pmc: PMC9977777
doi:

Substances chimiques

Liposomes 0
Ascorbic Acid PQ6CK8PD0R

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3448

Informations de copyright

© 2023. The Author(s).

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Auteurs

Anita Csorba (A)

Department of Ophthalmology, Semmelweis University, Mária Street 39., 1085, Budapest, Hungary.

Gábor Katona (G)

Institute of Pharmaceutical Technology and Regulatory Affairs, Faculty of Pharmacy, University of Szeged, Eötvös Street 6., 6720, Szeged, Hungary.

Mária Budai-Szűcs (M)

Institute of Pharmaceutical Technology and Regulatory Affairs, Faculty of Pharmacy, University of Szeged, Eötvös Street 6., 6720, Szeged, Hungary.

Diána Balogh-Weiser (D)

Department of Physical Chemistry and Materials Science, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Műegyetem Rkp. 3., 1111, Budapest, Hungary.

Anna Maria Fadda (AM)

Department of Life and Environmental Sciences, University of Cagliari, Via Ospedale 72, 09124, Cagliari, Italy.

Carla Caddeo (C)

Department of Life and Environmental Sciences, University of Cagliari, Via Ospedale 72, 09124, Cagliari, Italy.

Ágnes Ildikó Takács (ÁI)

Department of Ophthalmology, Semmelweis University, Mária Street 39., 1085, Budapest, Hungary.

Péter Mátyus (P)

E-Group ICT SOFTWARE, Kacsa Street 11, 1027, Budapest, Hungary.

György T Balogh (GT)

Department of Chemical and Process Engineering, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Műegyetem Rkp. 3., 1111, Budapest, Hungary. balogh.gyorgy@vbk.bme.hu.
Institute of Pharmacodynamics and Biopharmacy, Faculty of Pharmacy, University of Szeged, Eötvös Street 6., 6720, Szeged, Hungary. balogh.gyorgy@vbk.bme.hu.

Zoltán Zsolt Nagy (ZZ)

Department of Ophthalmology, Semmelweis University, Mária Street 39., 1085, Budapest, Hungary. nagy.zoltan_zsolt@med.semmelweis-univ.hu.

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Classifications MeSH