Cargando…

Functionalized Fluorescent Silica Nanoparticles for Bioimaging of Cancer Cells

Functionalized fluorescent silica nanoparticles were designed and synthesized to selectively target cancer cells for bioimaging analysis. The synthesis method and characterization of functionalized fluorescent silica nanoparticles (50–60 nm), as well as internalization and subcellular localization i...

Descripción completa

Detalles Bibliográficos
Autores principales: Prieto-Montero, Ruth, Katsumiti, Alberto, Cajaraville, Miren Pilare, López-Arbeloa, Iñigo, Martínez-Martínez, Virginia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582890/
https://www.ncbi.nlm.nih.gov/pubmed/33003513
http://dx.doi.org/10.3390/s20195590
_version_ 1783599295020138496
author Prieto-Montero, Ruth
Katsumiti, Alberto
Cajaraville, Miren Pilare
López-Arbeloa, Iñigo
Martínez-Martínez, Virginia
author_facet Prieto-Montero, Ruth
Katsumiti, Alberto
Cajaraville, Miren Pilare
López-Arbeloa, Iñigo
Martínez-Martínez, Virginia
author_sort Prieto-Montero, Ruth
collection PubMed
description Functionalized fluorescent silica nanoparticles were designed and synthesized to selectively target cancer cells for bioimaging analysis. The synthesis method and characterization of functionalized fluorescent silica nanoparticles (50–60 nm), as well as internalization and subcellular localization in HeLa cells is reported here. The dye, rhodamine 101 (R101) was physically embedded during the sol–gel synthesis. The dye loading was optimized by varying the synthesis conditions (temperature and dye concentration added to the gel) and by the use of different organotriethoxysilanes as a second silica precursor. Additionally, R101, was also covalently bound to the functionalized external surface of the silica nanoparticles. The quantum yields of the dye-doped silica nanoparticles range from 0.25 to 0.50 and demonstrated an enhanced brightness of 230–260 fold respect to the free dye in solution. The shell of the nanoparticles was further decorated with PEG of 2000 Da and folic acid (FA) to ensure good stability in water and to enhance selectivity to cancer cells, respectively. In vitro assays with HeLa cells showed that fluorescent nanoparticles were internalized by cells accumulating exclusively into lysosomes. Quantitative analysis showed a significantly higher accumulation of FA functionalized fluorescent silica nanoparticles compared to nanoparticles without FA, proving that the former may represent good candidates for targeting cancer cells.
format Online
Article
Text
id pubmed-7582890
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-75828902020-10-28 Functionalized Fluorescent Silica Nanoparticles for Bioimaging of Cancer Cells Prieto-Montero, Ruth Katsumiti, Alberto Cajaraville, Miren Pilare López-Arbeloa, Iñigo Martínez-Martínez, Virginia Sensors (Basel) Article Functionalized fluorescent silica nanoparticles were designed and synthesized to selectively target cancer cells for bioimaging analysis. The synthesis method and characterization of functionalized fluorescent silica nanoparticles (50–60 nm), as well as internalization and subcellular localization in HeLa cells is reported here. The dye, rhodamine 101 (R101) was physically embedded during the sol–gel synthesis. The dye loading was optimized by varying the synthesis conditions (temperature and dye concentration added to the gel) and by the use of different organotriethoxysilanes as a second silica precursor. Additionally, R101, was also covalently bound to the functionalized external surface of the silica nanoparticles. The quantum yields of the dye-doped silica nanoparticles range from 0.25 to 0.50 and demonstrated an enhanced brightness of 230–260 fold respect to the free dye in solution. The shell of the nanoparticles was further decorated with PEG of 2000 Da and folic acid (FA) to ensure good stability in water and to enhance selectivity to cancer cells, respectively. In vitro assays with HeLa cells showed that fluorescent nanoparticles were internalized by cells accumulating exclusively into lysosomes. Quantitative analysis showed a significantly higher accumulation of FA functionalized fluorescent silica nanoparticles compared to nanoparticles without FA, proving that the former may represent good candidates for targeting cancer cells. MDPI 2020-09-29 /pmc/articles/PMC7582890/ /pubmed/33003513 http://dx.doi.org/10.3390/s20195590 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
Prieto-Montero, Ruth
Katsumiti, Alberto
Cajaraville, Miren Pilare
López-Arbeloa, Iñigo
Martínez-Martínez, Virginia
Functionalized Fluorescent Silica Nanoparticles for Bioimaging of Cancer Cells
title Functionalized Fluorescent Silica Nanoparticles for Bioimaging of Cancer Cells
title_full Functionalized Fluorescent Silica Nanoparticles for Bioimaging of Cancer Cells
title_fullStr Functionalized Fluorescent Silica Nanoparticles for Bioimaging of Cancer Cells
title_full_unstemmed Functionalized Fluorescent Silica Nanoparticles for Bioimaging of Cancer Cells
title_short Functionalized Fluorescent Silica Nanoparticles for Bioimaging of Cancer Cells
title_sort functionalized fluorescent silica nanoparticles for bioimaging of cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582890/
https://www.ncbi.nlm.nih.gov/pubmed/33003513
http://dx.doi.org/10.3390/s20195590
work_keys_str_mv AT prietomonteroruth functionalizedfluorescentsilicananoparticlesforbioimagingofcancercells
AT katsumitialberto functionalizedfluorescentsilicananoparticlesforbioimagingofcancercells
AT cajaravillemirenpilare functionalizedfluorescentsilicananoparticlesforbioimagingofcancercells
AT lopezarbeloainigo functionalizedfluorescentsilicananoparticlesforbioimagingofcancercells
AT martinezmartinezvirginia functionalizedfluorescentsilicananoparticlesforbioimagingofcancercells