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Development of Artificial Plasma Membranes Derived Nanovesicles Suitable for Drugs Encapsulation
Extracellular vesicles (EVs) are considered as promising nanoparticle theranostic tools in many pathological contexts. The increasing clinical employment of therapeutic nanoparticles is contributing to the development of a new research area related to the design of artificial EVs. To this aim, diffe...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408059/ https://www.ncbi.nlm.nih.gov/pubmed/32640653 http://dx.doi.org/10.3390/cells9071626 |
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author | Martinelli, Carolina Gabriele, Fabio Dini, Elena Carriero, Francesca Bresciani, Giorgia Slivinschi, Bianca Dei Giudici, Marco Zanoletti, Lisa Manai, Federico Paolillo, Mayra Schinelli, Sergio Azzalin, Alberto Comincini, Sergio |
author_facet | Martinelli, Carolina Gabriele, Fabio Dini, Elena Carriero, Francesca Bresciani, Giorgia Slivinschi, Bianca Dei Giudici, Marco Zanoletti, Lisa Manai, Federico Paolillo, Mayra Schinelli, Sergio Azzalin, Alberto Comincini, Sergio |
author_sort | Martinelli, Carolina |
collection | PubMed |
description | Extracellular vesicles (EVs) are considered as promising nanoparticle theranostic tools in many pathological contexts. The increasing clinical employment of therapeutic nanoparticles is contributing to the development of a new research area related to the design of artificial EVs. To this aim, different approaches have been described to develop mimetic biologically functional nanovescicles. In this paper, we suggest a simplified procedure to generate plasma membrane-derived nanovesicles with the possibility to efficiently encapsulate different drugs during their spontaneously assembly. After physical and molecular characterization by Tunable Resistive Pulse Sensing (TRPS) technology, transmission electron microscopy, and flow cytometry, as a proof of principle, we have loaded into mimetic EVs the isoquinoline alkaloid Berberine chloride and the chemotherapy compounds Temozolomide or Givinostat. We demonstrated the fully functionality of these nanoparticles in drug encapsulation and cell delivery, showing, in particular, a similar cytotoxic effect of direct cell culture administration of the anticancer drugs. In conclusion, we have documented the possibility to easily generate scalable nanovesicles with specific therapeutic cargo modifications useful in different drug delivery contexts. |
format | Online Article Text |
id | pubmed-7408059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74080592020-08-25 Development of Artificial Plasma Membranes Derived Nanovesicles Suitable for Drugs Encapsulation Martinelli, Carolina Gabriele, Fabio Dini, Elena Carriero, Francesca Bresciani, Giorgia Slivinschi, Bianca Dei Giudici, Marco Zanoletti, Lisa Manai, Federico Paolillo, Mayra Schinelli, Sergio Azzalin, Alberto Comincini, Sergio Cells Article Extracellular vesicles (EVs) are considered as promising nanoparticle theranostic tools in many pathological contexts. The increasing clinical employment of therapeutic nanoparticles is contributing to the development of a new research area related to the design of artificial EVs. To this aim, different approaches have been described to develop mimetic biologically functional nanovescicles. In this paper, we suggest a simplified procedure to generate plasma membrane-derived nanovesicles with the possibility to efficiently encapsulate different drugs during their spontaneously assembly. After physical and molecular characterization by Tunable Resistive Pulse Sensing (TRPS) technology, transmission electron microscopy, and flow cytometry, as a proof of principle, we have loaded into mimetic EVs the isoquinoline alkaloid Berberine chloride and the chemotherapy compounds Temozolomide or Givinostat. We demonstrated the fully functionality of these nanoparticles in drug encapsulation and cell delivery, showing, in particular, a similar cytotoxic effect of direct cell culture administration of the anticancer drugs. In conclusion, we have documented the possibility to easily generate scalable nanovesicles with specific therapeutic cargo modifications useful in different drug delivery contexts. MDPI 2020-07-06 /pmc/articles/PMC7408059/ /pubmed/32640653 http://dx.doi.org/10.3390/cells9071626 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Martinelli, Carolina Gabriele, Fabio Dini, Elena Carriero, Francesca Bresciani, Giorgia Slivinschi, Bianca Dei Giudici, Marco Zanoletti, Lisa Manai, Federico Paolillo, Mayra Schinelli, Sergio Azzalin, Alberto Comincini, Sergio Development of Artificial Plasma Membranes Derived Nanovesicles Suitable for Drugs Encapsulation |
title | Development of Artificial Plasma Membranes Derived Nanovesicles Suitable for Drugs Encapsulation |
title_full | Development of Artificial Plasma Membranes Derived Nanovesicles Suitable for Drugs Encapsulation |
title_fullStr | Development of Artificial Plasma Membranes Derived Nanovesicles Suitable for Drugs Encapsulation |
title_full_unstemmed | Development of Artificial Plasma Membranes Derived Nanovesicles Suitable for Drugs Encapsulation |
title_short | Development of Artificial Plasma Membranes Derived Nanovesicles Suitable for Drugs Encapsulation |
title_sort | development of artificial plasma membranes derived nanovesicles suitable for drugs encapsulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408059/ https://www.ncbi.nlm.nih.gov/pubmed/32640653 http://dx.doi.org/10.3390/cells9071626 |
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