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Innovative Nanoparticles Enhance N-Palmitoylethanolamide Intraocular Delivery
Nanostructured lipid carriers (NLCs) loaded with palmitoylethanolamide (PEA) were formulated with the aim to enhance ocular bioavailability of PEA, particularly to the back of the eye. Technological characterization (e.g., size, charge) of NLC loaded with PEA formulation (PEA-NLC) was performed, and...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882782/ https://www.ncbi.nlm.nih.gov/pubmed/29643808 http://dx.doi.org/10.3389/fphar.2018.00285 |
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author | Puglia, Carmelo Blasi, Paolo Ostacolo, Carmine Sommella, Eduardo Bucolo, Claudio Platania, Chiara B. M. Romano, Giovanni L. Geraci, Federica Drago, Filippo Santonocito, Debora Albertini, Barbara Campiglia, Pietro Puglisi, Giovanni Pignatello, Rosario |
author_facet | Puglia, Carmelo Blasi, Paolo Ostacolo, Carmine Sommella, Eduardo Bucolo, Claudio Platania, Chiara B. M. Romano, Giovanni L. Geraci, Federica Drago, Filippo Santonocito, Debora Albertini, Barbara Campiglia, Pietro Puglisi, Giovanni Pignatello, Rosario |
author_sort | Puglia, Carmelo |
collection | PubMed |
description | Nanostructured lipid carriers (NLCs) loaded with palmitoylethanolamide (PEA) were formulated with the aim to enhance ocular bioavailability of PEA, particularly to the back of the eye. Technological characterization (e.g., size, charge) of NLC loaded with PEA formulation (PEA-NLC) was performed, and NLC morphology was characterized by electron microscopy. Ocular pharmacokinetic study, after topical administration of the formulation, was carried out in rabbit eye. Ultra-high performance liquid chromatography tandem mass spectrometry analysis was carried out to detect PEA levels in ocular tissues. Finally, the ocular tolerability of PEA-NLC formulation was assessed in rabbit eye. The novel formulation significantly increased PEA levels in ocular tissues compared to PEA suspension. Vitreous and retinal levels of PEA were significantly higher in the group treated with PEA-NLC formulation versus PEA suspension (PEA-NLC C(max) 5919 ± 541 pmol/g and 315 ± 70 pmol/g in vitreous and retina, respectively). The PEA-NLC formulation was characterized by high stability and robust ocular bioavailability. Therefore, this innovative formulation may be useful in clinical practice to manage retinal diseases. |
format | Online Article Text |
id | pubmed-5882782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58827822018-04-11 Innovative Nanoparticles Enhance N-Palmitoylethanolamide Intraocular Delivery Puglia, Carmelo Blasi, Paolo Ostacolo, Carmine Sommella, Eduardo Bucolo, Claudio Platania, Chiara B. M. Romano, Giovanni L. Geraci, Federica Drago, Filippo Santonocito, Debora Albertini, Barbara Campiglia, Pietro Puglisi, Giovanni Pignatello, Rosario Front Pharmacol Pharmacology Nanostructured lipid carriers (NLCs) loaded with palmitoylethanolamide (PEA) were formulated with the aim to enhance ocular bioavailability of PEA, particularly to the back of the eye. Technological characterization (e.g., size, charge) of NLC loaded with PEA formulation (PEA-NLC) was performed, and NLC morphology was characterized by electron microscopy. Ocular pharmacokinetic study, after topical administration of the formulation, was carried out in rabbit eye. Ultra-high performance liquid chromatography tandem mass spectrometry analysis was carried out to detect PEA levels in ocular tissues. Finally, the ocular tolerability of PEA-NLC formulation was assessed in rabbit eye. The novel formulation significantly increased PEA levels in ocular tissues compared to PEA suspension. Vitreous and retinal levels of PEA were significantly higher in the group treated with PEA-NLC formulation versus PEA suspension (PEA-NLC C(max) 5919 ± 541 pmol/g and 315 ± 70 pmol/g in vitreous and retina, respectively). The PEA-NLC formulation was characterized by high stability and robust ocular bioavailability. Therefore, this innovative formulation may be useful in clinical practice to manage retinal diseases. Frontiers Media S.A. 2018-03-28 /pmc/articles/PMC5882782/ /pubmed/29643808 http://dx.doi.org/10.3389/fphar.2018.00285 Text en Copyright © 2018 Puglia, Blasi, Ostacolo, Sommella, Bucolo, Platania, Romano, Geraci, Drago, Santonocito, Albertini, Campiglia, Puglisi and Pignatello. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Puglia, Carmelo Blasi, Paolo Ostacolo, Carmine Sommella, Eduardo Bucolo, Claudio Platania, Chiara B. M. Romano, Giovanni L. Geraci, Federica Drago, Filippo Santonocito, Debora Albertini, Barbara Campiglia, Pietro Puglisi, Giovanni Pignatello, Rosario Innovative Nanoparticles Enhance N-Palmitoylethanolamide Intraocular Delivery |
title | Innovative Nanoparticles Enhance N-Palmitoylethanolamide Intraocular Delivery |
title_full | Innovative Nanoparticles Enhance N-Palmitoylethanolamide Intraocular Delivery |
title_fullStr | Innovative Nanoparticles Enhance N-Palmitoylethanolamide Intraocular Delivery |
title_full_unstemmed | Innovative Nanoparticles Enhance N-Palmitoylethanolamide Intraocular Delivery |
title_short | Innovative Nanoparticles Enhance N-Palmitoylethanolamide Intraocular Delivery |
title_sort | innovative nanoparticles enhance n-palmitoylethanolamide intraocular delivery |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882782/ https://www.ncbi.nlm.nih.gov/pubmed/29643808 http://dx.doi.org/10.3389/fphar.2018.00285 |
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