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Silicon particles as trojan horses for potential cancer therapy
BACKGROUND: Porous silicon particles (PSiPs) have been used extensively as drug delivery systems, loaded with chemical species for disease treatment. It is well known from silicon producers that silicon is characterized by a low reduction potential, which in the case of PSiPs promotes explosive oxid...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428529/ https://www.ncbi.nlm.nih.gov/pubmed/25223512 http://dx.doi.org/10.1186/s12951-014-0035-7 |
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author | Fenollosa, Roberto Garcia-Rico, Eduardo Alvarez, Susana Alvarez, Rosana Yu, Xiang Rodriguez, Isabel Carregal-Romero, Susana Villanueva, Carlos Garcia-Algar, Manuel Rivera-Gil, Pilar de Lera, Angel R Parak, Wolfgang J Meseguer, Francisco Alvarez-Puebla, Ramón A |
author_facet | Fenollosa, Roberto Garcia-Rico, Eduardo Alvarez, Susana Alvarez, Rosana Yu, Xiang Rodriguez, Isabel Carregal-Romero, Susana Villanueva, Carlos Garcia-Algar, Manuel Rivera-Gil, Pilar de Lera, Angel R Parak, Wolfgang J Meseguer, Francisco Alvarez-Puebla, Ramón A |
author_sort | Fenollosa, Roberto |
collection | PubMed |
description | BACKGROUND: Porous silicon particles (PSiPs) have been used extensively as drug delivery systems, loaded with chemical species for disease treatment. It is well known from silicon producers that silicon is characterized by a low reduction potential, which in the case of PSiPs promotes explosive oxidation reactions with energy yields exceeding that of trinitrotoluene (TNT). The functionalization of the silica layer with sugars prevents its solubilization, while further functionalization with an appropriate antibody enables increased bioaccumulation inside selected cells. RESULTS: We present here an immunotherapy approach for potential cancer treatment. Our platform comprises the use of engineered silicon particles conjugated with a selective antibody. The conceptual advantage of our system is that after reaction, the particles are degraded into soluble and excretable biocomponents. CONCLUSIONS: In our study, we demonstrate in particular, specific targeting and destruction of cancer cells in vitro. The fact that the LD(50) value of PSiPs-HER-2 for tumor cells was 15-fold lower than the LD(50) value for control cells demonstrates very high in vitro specificity. This is the first important step on a long road towards the design and development of novel chemotherapeutic agents against cancer in general, and breast cancer in particular. |
format | Online Article Text |
id | pubmed-4428529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44285292015-05-13 Silicon particles as trojan horses for potential cancer therapy Fenollosa, Roberto Garcia-Rico, Eduardo Alvarez, Susana Alvarez, Rosana Yu, Xiang Rodriguez, Isabel Carregal-Romero, Susana Villanueva, Carlos Garcia-Algar, Manuel Rivera-Gil, Pilar de Lera, Angel R Parak, Wolfgang J Meseguer, Francisco Alvarez-Puebla, Ramón A J Nanobiotechnology Research BACKGROUND: Porous silicon particles (PSiPs) have been used extensively as drug delivery systems, loaded with chemical species for disease treatment. It is well known from silicon producers that silicon is characterized by a low reduction potential, which in the case of PSiPs promotes explosive oxidation reactions with energy yields exceeding that of trinitrotoluene (TNT). The functionalization of the silica layer with sugars prevents its solubilization, while further functionalization with an appropriate antibody enables increased bioaccumulation inside selected cells. RESULTS: We present here an immunotherapy approach for potential cancer treatment. Our platform comprises the use of engineered silicon particles conjugated with a selective antibody. The conceptual advantage of our system is that after reaction, the particles are degraded into soluble and excretable biocomponents. CONCLUSIONS: In our study, we demonstrate in particular, specific targeting and destruction of cancer cells in vitro. The fact that the LD(50) value of PSiPs-HER-2 for tumor cells was 15-fold lower than the LD(50) value for control cells demonstrates very high in vitro specificity. This is the first important step on a long road towards the design and development of novel chemotherapeutic agents against cancer in general, and breast cancer in particular. BioMed Central 2014-09-16 /pmc/articles/PMC4428529/ /pubmed/25223512 http://dx.doi.org/10.1186/s12951-014-0035-7 Text en © Fenollosa et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Fenollosa, Roberto Garcia-Rico, Eduardo Alvarez, Susana Alvarez, Rosana Yu, Xiang Rodriguez, Isabel Carregal-Romero, Susana Villanueva, Carlos Garcia-Algar, Manuel Rivera-Gil, Pilar de Lera, Angel R Parak, Wolfgang J Meseguer, Francisco Alvarez-Puebla, Ramón A Silicon particles as trojan horses for potential cancer therapy |
title | Silicon particles as trojan horses for potential cancer therapy |
title_full | Silicon particles as trojan horses for potential cancer therapy |
title_fullStr | Silicon particles as trojan horses for potential cancer therapy |
title_full_unstemmed | Silicon particles as trojan horses for potential cancer therapy |
title_short | Silicon particles as trojan horses for potential cancer therapy |
title_sort | silicon particles as trojan horses for potential cancer therapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428529/ https://www.ncbi.nlm.nih.gov/pubmed/25223512 http://dx.doi.org/10.1186/s12951-014-0035-7 |
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