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Nanostructured ultra-thin patches for ultrasound-modulated delivery of anti-restenotic drug

This work aims to demonstrate the possibility to fabricate ultra-thin polymeric films loaded with an anti-restenotic drug and capable of tunable drug release kinetics for the local treatment of restenosis. Vascular nanopatches are composed of a poly(lactic acid) supporting membrane (thickness: ~250...

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Autores principales: Vannozzi, Lorenzo, Ricotti, Leonardo, Filippeschi, Carlo, Sartini, Stefania, Coviello, Vito, Piazza, Vincenzo, Pingue, Pasqualantonio, La Motta, Concettina, Dario, Paolo, Menciassi, Arianna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694686/
https://www.ncbi.nlm.nih.gov/pubmed/26730191
http://dx.doi.org/10.2147/IJN.S92031
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author Vannozzi, Lorenzo
Ricotti, Leonardo
Filippeschi, Carlo
Sartini, Stefania
Coviello, Vito
Piazza, Vincenzo
Pingue, Pasqualantonio
La Motta, Concettina
Dario, Paolo
Menciassi, Arianna
author_facet Vannozzi, Lorenzo
Ricotti, Leonardo
Filippeschi, Carlo
Sartini, Stefania
Coviello, Vito
Piazza, Vincenzo
Pingue, Pasqualantonio
La Motta, Concettina
Dario, Paolo
Menciassi, Arianna
author_sort Vannozzi, Lorenzo
collection PubMed
description This work aims to demonstrate the possibility to fabricate ultra-thin polymeric films loaded with an anti-restenotic drug and capable of tunable drug release kinetics for the local treatment of restenosis. Vascular nanopatches are composed of a poly(lactic acid) supporting membrane (thickness: ~250 nm) on which 20 polyelectrolyte bilayers (overall thickness: ~70 nm) are alternatively deposited. The anti-restenotic drug is embedded in the middle of the polyelectrolyte structure, and released by diffusion mechanisms. Nanofilm fabrication procedure and detailed morphological characterization are reported here. Barium titanate nanoparticles (showing piezoelectric properties) are included in the polymeric support and their role is investigated in terms of influence on nanofilm morphology, drug release kinetics, and cell response. Results show an efficient drug release from the polyelectrolyte structure in phosphate-buffered saline, and a clear antiproliferative effect on human smooth muscle cells, which are responsible for restenosis. In addition, preliminary evidences of ultrasound-mediated modulation of drug release kinetics are reported, thus evaluating the influence of barium titanate nanoparticles on the release mechanism. Such data were integrated with quantitative piezoelectric and thermal measurements. These results open new avenues for a fine control of local therapies based on smart responsive materials.
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spelling pubmed-46946862016-01-04 Nanostructured ultra-thin patches for ultrasound-modulated delivery of anti-restenotic drug Vannozzi, Lorenzo Ricotti, Leonardo Filippeschi, Carlo Sartini, Stefania Coviello, Vito Piazza, Vincenzo Pingue, Pasqualantonio La Motta, Concettina Dario, Paolo Menciassi, Arianna Int J Nanomedicine Original Research This work aims to demonstrate the possibility to fabricate ultra-thin polymeric films loaded with an anti-restenotic drug and capable of tunable drug release kinetics for the local treatment of restenosis. Vascular nanopatches are composed of a poly(lactic acid) supporting membrane (thickness: ~250 nm) on which 20 polyelectrolyte bilayers (overall thickness: ~70 nm) are alternatively deposited. The anti-restenotic drug is embedded in the middle of the polyelectrolyte structure, and released by diffusion mechanisms. Nanofilm fabrication procedure and detailed morphological characterization are reported here. Barium titanate nanoparticles (showing piezoelectric properties) are included in the polymeric support and their role is investigated in terms of influence on nanofilm morphology, drug release kinetics, and cell response. Results show an efficient drug release from the polyelectrolyte structure in phosphate-buffered saline, and a clear antiproliferative effect on human smooth muscle cells, which are responsible for restenosis. In addition, preliminary evidences of ultrasound-mediated modulation of drug release kinetics are reported, thus evaluating the influence of barium titanate nanoparticles on the release mechanism. Such data were integrated with quantitative piezoelectric and thermal measurements. These results open new avenues for a fine control of local therapies based on smart responsive materials. Dove Medical Press 2015-12-23 /pmc/articles/PMC4694686/ /pubmed/26730191 http://dx.doi.org/10.2147/IJN.S92031 Text en © 2016 Vannozzi et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Vannozzi, Lorenzo
Ricotti, Leonardo
Filippeschi, Carlo
Sartini, Stefania
Coviello, Vito
Piazza, Vincenzo
Pingue, Pasqualantonio
La Motta, Concettina
Dario, Paolo
Menciassi, Arianna
Nanostructured ultra-thin patches for ultrasound-modulated delivery of anti-restenotic drug
title Nanostructured ultra-thin patches for ultrasound-modulated delivery of anti-restenotic drug
title_full Nanostructured ultra-thin patches for ultrasound-modulated delivery of anti-restenotic drug
title_fullStr Nanostructured ultra-thin patches for ultrasound-modulated delivery of anti-restenotic drug
title_full_unstemmed Nanostructured ultra-thin patches for ultrasound-modulated delivery of anti-restenotic drug
title_short Nanostructured ultra-thin patches for ultrasound-modulated delivery of anti-restenotic drug
title_sort nanostructured ultra-thin patches for ultrasound-modulated delivery of anti-restenotic drug
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694686/
https://www.ncbi.nlm.nih.gov/pubmed/26730191
http://dx.doi.org/10.2147/IJN.S92031
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