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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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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. |
format | Online Article Text |
id | pubmed-10143234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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