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Cell-Penetrating CaCO(3) Nanocrystals for Improved Transport of NVP-BEZ235 across Membrane Barrier in T-Cell Lymphoma
Owing to their nano-sized porous structure, CaCO(3) nanocrystals (CaCO(3)NCs) hold the promise to be utilized as desired materials for encapsulating molecules which demonstrate wide promise in drug delivery. We evaluate the possibility to encapsulate and release NVP-BEZ235, a novel and potent dual P...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836063/ https://www.ncbi.nlm.nih.gov/pubmed/29370086 http://dx.doi.org/10.3390/cancers10020031 |
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author | Vergaro, Viviana Civallero, Monica Citti, Cinzia Cosenza, Maria Baldassarre, Francesca Cannazza, Giuseppe Pozzi, Samantha Sacchi, Stefano Fanizzi, Francesco Paolo Ciccarella, Giuseppe |
author_facet | Vergaro, Viviana Civallero, Monica Citti, Cinzia Cosenza, Maria Baldassarre, Francesca Cannazza, Giuseppe Pozzi, Samantha Sacchi, Stefano Fanizzi, Francesco Paolo Ciccarella, Giuseppe |
author_sort | Vergaro, Viviana |
collection | PubMed |
description | Owing to their nano-sized porous structure, CaCO(3) nanocrystals (CaCO(3)NCs) hold the promise to be utilized as desired materials for encapsulating molecules which demonstrate wide promise in drug delivery. We evaluate the possibility to encapsulate and release NVP-BEZ235, a novel and potent dual PI3K/mTOR inhibitor that is currently in phase I/II clinical trials for advanced solid tumors, from the CaCO(3)NCs. Its chemical nature shows some intrinsic limitations which induce to administer high doses leading to toxicity; to overcome these problems, here we proposed a strategy to enhance its intracellular penetration and its biological activity. Pristine CaCO(3) NCs biocompatibility, cell interactions and internalization in in vitro experiments on T-cell lymphoma line, were studied. Confocal microscopy was used to monitor NCs-cell interactions and cellular uptake. We have further investigated the interaction nature and release mechanism of drug loaded/released within/from the NCs using an alternative approach based on liquid chromatography coupled to mass spectrometry. Our approach provides a good loading efficiency, therefore this drug delivery system was validated for biological activity in T-cell lymphoma: the anti-proliferative test and western blot results are very interesting because the proposed nano-formulation has an efficiency higher than free drug at the same nominal concentration. |
format | Online Article Text |
id | pubmed-5836063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-58360632018-03-07 Cell-Penetrating CaCO(3) Nanocrystals for Improved Transport of NVP-BEZ235 across Membrane Barrier in T-Cell Lymphoma Vergaro, Viviana Civallero, Monica Citti, Cinzia Cosenza, Maria Baldassarre, Francesca Cannazza, Giuseppe Pozzi, Samantha Sacchi, Stefano Fanizzi, Francesco Paolo Ciccarella, Giuseppe Cancers (Basel) Article Owing to their nano-sized porous structure, CaCO(3) nanocrystals (CaCO(3)NCs) hold the promise to be utilized as desired materials for encapsulating molecules which demonstrate wide promise in drug delivery. We evaluate the possibility to encapsulate and release NVP-BEZ235, a novel and potent dual PI3K/mTOR inhibitor that is currently in phase I/II clinical trials for advanced solid tumors, from the CaCO(3)NCs. Its chemical nature shows some intrinsic limitations which induce to administer high doses leading to toxicity; to overcome these problems, here we proposed a strategy to enhance its intracellular penetration and its biological activity. Pristine CaCO(3) NCs biocompatibility, cell interactions and internalization in in vitro experiments on T-cell lymphoma line, were studied. Confocal microscopy was used to monitor NCs-cell interactions and cellular uptake. We have further investigated the interaction nature and release mechanism of drug loaded/released within/from the NCs using an alternative approach based on liquid chromatography coupled to mass spectrometry. Our approach provides a good loading efficiency, therefore this drug delivery system was validated for biological activity in T-cell lymphoma: the anti-proliferative test and western blot results are very interesting because the proposed nano-formulation has an efficiency higher than free drug at the same nominal concentration. MDPI 2018-01-25 /pmc/articles/PMC5836063/ /pubmed/29370086 http://dx.doi.org/10.3390/cancers10020031 Text en © 2018 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 Vergaro, Viviana Civallero, Monica Citti, Cinzia Cosenza, Maria Baldassarre, Francesca Cannazza, Giuseppe Pozzi, Samantha Sacchi, Stefano Fanizzi, Francesco Paolo Ciccarella, Giuseppe Cell-Penetrating CaCO(3) Nanocrystals for Improved Transport of NVP-BEZ235 across Membrane Barrier in T-Cell Lymphoma |
title | Cell-Penetrating CaCO(3) Nanocrystals for Improved Transport of NVP-BEZ235 across Membrane Barrier in T-Cell Lymphoma |
title_full | Cell-Penetrating CaCO(3) Nanocrystals for Improved Transport of NVP-BEZ235 across Membrane Barrier in T-Cell Lymphoma |
title_fullStr | Cell-Penetrating CaCO(3) Nanocrystals for Improved Transport of NVP-BEZ235 across Membrane Barrier in T-Cell Lymphoma |
title_full_unstemmed | Cell-Penetrating CaCO(3) Nanocrystals for Improved Transport of NVP-BEZ235 across Membrane Barrier in T-Cell Lymphoma |
title_short | Cell-Penetrating CaCO(3) Nanocrystals for Improved Transport of NVP-BEZ235 across Membrane Barrier in T-Cell Lymphoma |
title_sort | cell-penetrating caco(3) nanocrystals for improved transport of nvp-bez235 across membrane barrier in t-cell lymphoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836063/ https://www.ncbi.nlm.nih.gov/pubmed/29370086 http://dx.doi.org/10.3390/cancers10020031 |
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