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Development of Nanofibers with Embedded Liposomes Containing an Immunomodulatory Drug Using Green Electrospinning
Conventional treatments for chronic wounds are often ineffective, thus new therapeutic approaches are needed, such as the delivery of immunomodulatory drugs that can reduce inflammation, restore immune cell function, and facilitate tissue regeneration. A potential drug for such an approach is simvas...
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/PMC10143873/ https://www.ncbi.nlm.nih.gov/pubmed/37111731 http://dx.doi.org/10.3390/pharmaceutics15041245 |
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author | Casula, Luca Zidar, Anže Kristl, Julijana Jeras, Matjaž Kralj, Slavko Fadda, Anna Maria Zupančič, Špela |
author_facet | Casula, Luca Zidar, Anže Kristl, Julijana Jeras, Matjaž Kralj, Slavko Fadda, Anna Maria Zupančič, Špela |
author_sort | Casula, Luca |
collection | PubMed |
description | Conventional treatments for chronic wounds are often ineffective, thus new therapeutic approaches are needed, such as the delivery of immunomodulatory drugs that can reduce inflammation, restore immune cell function, and facilitate tissue regeneration. A potential drug for such an approach is simvastatin, which has major drawbacks including poor solubility and chemical instability. With the aim of developing a dressing for wound healing, simvastatin and an antioxidant were incorporated into alginate/poly(ethylene oxide) nanofibers by green electrospinning without the use of organic solvents, thanks to their prior encapsulation into liposomes. The composite liposome–nanofiber formulations exhibited fibrillar morphology (160–312 nm) and unprecedentedly high phospholipid and drug content (76%). Transmission electron microscopy revealed dried liposomes as bright ellipsoidal spots homogeneously distributed over the nanofibers. After nanofiber hydration, the liposomes reconstituted in two size populations (~140 and ~435 nm), as revealed by cutting-edge MADLS(®) analysis. Lastly, in vitro assays demonstrated that composite liposome–nanofiber formulations are superior to liposomal formulations due to a better safety profile in keratinocytes and peripheral blood mononuclear cells. Furthermore, both formulations exhibited similarly advantageous immunomodulatory effects, measured as decreased inflammation in vitro. A synergistic combination of the two nanodelivery systems shows promise for the development of efficient dressings for chronic wound treatment. |
format | Online Article Text |
id | pubmed-10143873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101438732023-04-29 Development of Nanofibers with Embedded Liposomes Containing an Immunomodulatory Drug Using Green Electrospinning Casula, Luca Zidar, Anže Kristl, Julijana Jeras, Matjaž Kralj, Slavko Fadda, Anna Maria Zupančič, Špela Pharmaceutics Article Conventional treatments for chronic wounds are often ineffective, thus new therapeutic approaches are needed, such as the delivery of immunomodulatory drugs that can reduce inflammation, restore immune cell function, and facilitate tissue regeneration. A potential drug for such an approach is simvastatin, which has major drawbacks including poor solubility and chemical instability. With the aim of developing a dressing for wound healing, simvastatin and an antioxidant were incorporated into alginate/poly(ethylene oxide) nanofibers by green electrospinning without the use of organic solvents, thanks to their prior encapsulation into liposomes. The composite liposome–nanofiber formulations exhibited fibrillar morphology (160–312 nm) and unprecedentedly high phospholipid and drug content (76%). Transmission electron microscopy revealed dried liposomes as bright ellipsoidal spots homogeneously distributed over the nanofibers. After nanofiber hydration, the liposomes reconstituted in two size populations (~140 and ~435 nm), as revealed by cutting-edge MADLS(®) analysis. Lastly, in vitro assays demonstrated that composite liposome–nanofiber formulations are superior to liposomal formulations due to a better safety profile in keratinocytes and peripheral blood mononuclear cells. Furthermore, both formulations exhibited similarly advantageous immunomodulatory effects, measured as decreased inflammation in vitro. A synergistic combination of the two nanodelivery systems shows promise for the development of efficient dressings for chronic wound treatment. MDPI 2023-04-14 /pmc/articles/PMC10143873/ /pubmed/37111731 http://dx.doi.org/10.3390/pharmaceutics15041245 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 Casula, Luca Zidar, Anže Kristl, Julijana Jeras, Matjaž Kralj, Slavko Fadda, Anna Maria Zupančič, Špela Development of Nanofibers with Embedded Liposomes Containing an Immunomodulatory Drug Using Green Electrospinning |
title | Development of Nanofibers with Embedded Liposomes Containing an Immunomodulatory Drug Using Green Electrospinning |
title_full | Development of Nanofibers with Embedded Liposomes Containing an Immunomodulatory Drug Using Green Electrospinning |
title_fullStr | Development of Nanofibers with Embedded Liposomes Containing an Immunomodulatory Drug Using Green Electrospinning |
title_full_unstemmed | Development of Nanofibers with Embedded Liposomes Containing an Immunomodulatory Drug Using Green Electrospinning |
title_short | Development of Nanofibers with Embedded Liposomes Containing an Immunomodulatory Drug Using Green Electrospinning |
title_sort | development of nanofibers with embedded liposomes containing an immunomodulatory drug using green electrospinning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10143873/ https://www.ncbi.nlm.nih.gov/pubmed/37111731 http://dx.doi.org/10.3390/pharmaceutics15041245 |
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