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Applying in-situ visible photopolymerization for fabrication of electrospun nanofibrous carrier for meloxicam delivery

Despite meloxicam’s many benefits, it will cause many drawbacks if the meloxicam release rate is not controlled. Accordingly, we introduced a technique based on the electrospinning process to control the release rate and also to reduce side effects. For this purpose, different nanofibers were used a...

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Autores principales: Ahmadipour, Z., Seyed Dorraji, M. S., Ashjari, H. R., Dodangeh, F., Rasoulifard, M. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275867/
https://www.ncbi.nlm.nih.gov/pubmed/37328688
http://dx.doi.org/10.1038/s41598-023-36893-9
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author Ahmadipour, Z.
Seyed Dorraji, M. S.
Ashjari, H. R.
Dodangeh, F.
Rasoulifard, M. H.
author_facet Ahmadipour, Z.
Seyed Dorraji, M. S.
Ashjari, H. R.
Dodangeh, F.
Rasoulifard, M. H.
author_sort Ahmadipour, Z.
collection PubMed
description Despite meloxicam’s many benefits, it will cause many drawbacks if the meloxicam release rate is not controlled. Accordingly, we introduced a technique based on the electrospinning process to control the release rate and also to reduce side effects. For this purpose, different nanofibers were used as drug couriers. Nanofibers were prepared using polyurethane, polyethylene glycol, and light curable poly (ethylene glycol) diacrylate (PEGDA) by electrospinning. In fact, light curable poly (ethylene glycol) diacrylate (PEGDA) was synthesized as a hydrophilic functional group. Next, PEGDA and polyurethane were used simultaneously to fabricate the drug carrier nanofiber in a single processing step, and the electrospinning apparatus was equipped with a blue light source for in-situ photopolymerization during the electrospinning process. The molecular structures of nanofibers and PEGDA were investigated by FT-IR, (1)H NMR, (13)C NMR, SEM, TEM, XRD, and DSC analyses. Finally, we reduced in vitro drug release to 44% within ten hours, while the minimum release of meloxicam from the tablet was 98%.
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spelling pubmed-102758672023-06-18 Applying in-situ visible photopolymerization for fabrication of electrospun nanofibrous carrier for meloxicam delivery Ahmadipour, Z. Seyed Dorraji, M. S. Ashjari, H. R. Dodangeh, F. Rasoulifard, M. H. Sci Rep Article Despite meloxicam’s many benefits, it will cause many drawbacks if the meloxicam release rate is not controlled. Accordingly, we introduced a technique based on the electrospinning process to control the release rate and also to reduce side effects. For this purpose, different nanofibers were used as drug couriers. Nanofibers were prepared using polyurethane, polyethylene glycol, and light curable poly (ethylene glycol) diacrylate (PEGDA) by electrospinning. In fact, light curable poly (ethylene glycol) diacrylate (PEGDA) was synthesized as a hydrophilic functional group. Next, PEGDA and polyurethane were used simultaneously to fabricate the drug carrier nanofiber in a single processing step, and the electrospinning apparatus was equipped with a blue light source for in-situ photopolymerization during the electrospinning process. The molecular structures of nanofibers and PEGDA were investigated by FT-IR, (1)H NMR, (13)C NMR, SEM, TEM, XRD, and DSC analyses. Finally, we reduced in vitro drug release to 44% within ten hours, while the minimum release of meloxicam from the tablet was 98%. Nature Publishing Group UK 2023-06-16 /pmc/articles/PMC10275867/ /pubmed/37328688 http://dx.doi.org/10.1038/s41598-023-36893-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ahmadipour, Z.
Seyed Dorraji, M. S.
Ashjari, H. R.
Dodangeh, F.
Rasoulifard, M. H.
Applying in-situ visible photopolymerization for fabrication of electrospun nanofibrous carrier for meloxicam delivery
title Applying in-situ visible photopolymerization for fabrication of electrospun nanofibrous carrier for meloxicam delivery
title_full Applying in-situ visible photopolymerization for fabrication of electrospun nanofibrous carrier for meloxicam delivery
title_fullStr Applying in-situ visible photopolymerization for fabrication of electrospun nanofibrous carrier for meloxicam delivery
title_full_unstemmed Applying in-situ visible photopolymerization for fabrication of electrospun nanofibrous carrier for meloxicam delivery
title_short Applying in-situ visible photopolymerization for fabrication of electrospun nanofibrous carrier for meloxicam delivery
title_sort applying in-situ visible photopolymerization for fabrication of electrospun nanofibrous carrier for meloxicam delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275867/
https://www.ncbi.nlm.nih.gov/pubmed/37328688
http://dx.doi.org/10.1038/s41598-023-36893-9
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