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Formulation and Characterization of Electrospun Nanofibers for Melatonin Ocular Delivery

The poor ocular bioavailability of melatonin (MEL) limits the therapeutic action the molecule could exert in the treatment of ocular diseases. To date, no study has explored the use of nanofiber-based inserts to prolong ocular surface contact time and improve MEL delivery. Here, the electrospinning...

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Autores principales: Romeo, Alessia, Kazsoki, Adrienn, Omer, Safaa, Pinke, Balázs, Mészáros, László, Musumeci, Teresa, Zelkó, Romána
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10143234/
https://www.ncbi.nlm.nih.gov/pubmed/37111782
http://dx.doi.org/10.3390/pharmaceutics15041296
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author Romeo, Alessia
Kazsoki, Adrienn
Omer, Safaa
Pinke, Balázs
Mészáros, László
Musumeci, Teresa
Zelkó, Romána
author_facet Romeo, Alessia
Kazsoki, Adrienn
Omer, Safaa
Pinke, Balázs
Mészáros, László
Musumeci, Teresa
Zelkó, Romána
author_sort Romeo, Alessia
collection PubMed
description The poor ocular bioavailability of melatonin (MEL) limits the therapeutic action the molecule could exert in the treatment of ocular diseases. To date, no study has explored the use of nanofiber-based inserts to prolong ocular surface contact time and improve MEL delivery. Here, the electrospinning technique was proposed to prepare poly (vinyl alcohol) (PVA) and poly (lactic acid) (PLA) nanofiber inserts. Both nanofibers were produced with different concentrations of MEL and with or without the addition of Tween(®) 80. Nanofibers morphology was evaluated by scanning electron microscopy. Thermal and spectroscopic analyses were performed to characterize the state of MEL in the scaffolds. MEL release profiles were observed under simulated physiological conditions (pH 7.4, 37 °C). The swelling behavior was evaluated by a gravimetric method. The results confirmed that submicron-sized nanofibrous structures were obtained with MEL in the amorphous state. Different MEL release rates were achieved depending on the nature of the polymer. Fast (20 min) and complete release was observed for the PVA-based samples, unlike the PLA polymer, which provided slow and controlled MEL release. The addition of Tween(®) 80 affected the swelling properties of the fibrous structures. Overall, the results suggest that membranes could be an attractive vehicle as a potential alternative to liquid formulations for ocular administration of MEL.
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spelling pubmed-101432342023-04-29 Formulation and Characterization of Electrospun Nanofibers for Melatonin Ocular Delivery Romeo, Alessia Kazsoki, Adrienn Omer, Safaa Pinke, Balázs Mészáros, László Musumeci, Teresa Zelkó, Romána Pharmaceutics Article The poor ocular bioavailability of melatonin (MEL) limits the therapeutic action the molecule could exert in the treatment of ocular diseases. To date, no study has explored the use of nanofiber-based inserts to prolong ocular surface contact time and improve MEL delivery. Here, the electrospinning technique was proposed to prepare poly (vinyl alcohol) (PVA) and poly (lactic acid) (PLA) nanofiber inserts. Both nanofibers were produced with different concentrations of MEL and with or without the addition of Tween(®) 80. Nanofibers morphology was evaluated by scanning electron microscopy. Thermal and spectroscopic analyses were performed to characterize the state of MEL in the scaffolds. MEL release profiles were observed under simulated physiological conditions (pH 7.4, 37 °C). The swelling behavior was evaluated by a gravimetric method. The results confirmed that submicron-sized nanofibrous structures were obtained with MEL in the amorphous state. Different MEL release rates were achieved depending on the nature of the polymer. Fast (20 min) and complete release was observed for the PVA-based samples, unlike the PLA polymer, which provided slow and controlled MEL release. The addition of Tween(®) 80 affected the swelling properties of the fibrous structures. Overall, the results suggest that membranes could be an attractive vehicle as a potential alternative to liquid formulations for ocular administration of MEL. MDPI 2023-04-20 /pmc/articles/PMC10143234/ /pubmed/37111782 http://dx.doi.org/10.3390/pharmaceutics15041296 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Romeo, Alessia
Kazsoki, Adrienn
Omer, Safaa
Pinke, Balázs
Mészáros, László
Musumeci, Teresa
Zelkó, Romána
Formulation and Characterization of Electrospun Nanofibers for Melatonin Ocular Delivery
title Formulation and Characterization of Electrospun Nanofibers for Melatonin Ocular Delivery
title_full Formulation and Characterization of Electrospun Nanofibers for Melatonin Ocular Delivery
title_fullStr Formulation and Characterization of Electrospun Nanofibers for Melatonin Ocular Delivery
title_full_unstemmed Formulation and Characterization of Electrospun Nanofibers for Melatonin Ocular Delivery
title_short Formulation and Characterization of Electrospun Nanofibers for Melatonin Ocular Delivery
title_sort formulation and characterization of electrospun nanofibers for melatonin ocular delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10143234/
https://www.ncbi.nlm.nih.gov/pubmed/37111782
http://dx.doi.org/10.3390/pharmaceutics15041296
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