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Aminosilane Functionalization and Cytotoxicity Effects of Upconversion Nanoparticles Y(2)O(3) and Gd(2)O(3) Co-Doped with Yb(3+)and Er(3+)

In this study, luminescent upconversion nanoparticles (UCNPs) Y(2)O(3) and Gd(2)O(3) co-doped with Yb(3+) and Er(3+) were prepared by the sol-gel method (SG). These NPs are able to absorb near infrared photons and upconvert them into visible radiation with a direct application in bioimaging, as an i...

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Autores principales: Chavez, Dalia Holanda, Juarez-Moreno, Karla, Hirata, Gustavo Alonso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998266/
https://www.ncbi.nlm.nih.gov/pubmed/29942376
http://dx.doi.org/10.5772/62252
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author Chavez, Dalia Holanda
Juarez-Moreno, Karla
Hirata, Gustavo Alonso
author_facet Chavez, Dalia Holanda
Juarez-Moreno, Karla
Hirata, Gustavo Alonso
author_sort Chavez, Dalia Holanda
collection PubMed
description In this study, luminescent upconversion nanoparticles (UCNPs) Y(2)O(3) and Gd(2)O(3) co-doped with Yb(3+) and Er(3+) were prepared by the sol-gel method (SG). These NPs are able to absorb near infrared photons and upconvert them into visible radiation with a direct application in bioimaging, as an important tool to diagnose and visualize cancer cells. The UCNPs were coated with a thin silica shell and functionalized with amino groups for further folic acid conjugation to allow their interaction with folate ligands on the cell surface. Their physical properties were analysed by Transmission Electron Microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and photoluminescence (PL) measurements. The PL results revealed excellent luminescence properties on all core-shell UCNPs. Cytotoxicity experiments with concentrations of bare and aminosilane coated/functionalized UCNPs between 0.001 μg/mL to 1 μg/mL were tested on two different cell lines from human cervix carcinoma (HeLa) and human colorectal adenocarcinoma (DLD-1) with a colorimetric assay based on the reduction of MTT reagent (methy-134-thiazolyltetrazolium). The assays show that some concentrations of bare UCNPs were cytotoxic for cervical adenocarcinoma cells (HeLa); however, for human colorectal adenocarcinoma all UCNPs are non-cytotoxic. After UCNPs functionalization with silica-aminosilane (APTES/TEOS), all of the nanoparticles tested were found to be non-cytotoxic for both cell lines. The UCNPs functionalized in this work can be further conjugated with specific ligands and used as biolabels for detection of cancer cells.
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spelling pubmed-59982662018-06-25 Aminosilane Functionalization and Cytotoxicity Effects of Upconversion Nanoparticles Y(2)O(3) and Gd(2)O(3) Co-Doped with Yb(3+)and Er(3+) Chavez, Dalia Holanda Juarez-Moreno, Karla Hirata, Gustavo Alonso Nanobiomedicine (Rij) Nanobiomedicine In this study, luminescent upconversion nanoparticles (UCNPs) Y(2)O(3) and Gd(2)O(3) co-doped with Yb(3+) and Er(3+) were prepared by the sol-gel method (SG). These NPs are able to absorb near infrared photons and upconvert them into visible radiation with a direct application in bioimaging, as an important tool to diagnose and visualize cancer cells. The UCNPs were coated with a thin silica shell and functionalized with amino groups for further folic acid conjugation to allow their interaction with folate ligands on the cell surface. Their physical properties were analysed by Transmission Electron Microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and photoluminescence (PL) measurements. The PL results revealed excellent luminescence properties on all core-shell UCNPs. Cytotoxicity experiments with concentrations of bare and aminosilane coated/functionalized UCNPs between 0.001 μg/mL to 1 μg/mL were tested on two different cell lines from human cervix carcinoma (HeLa) and human colorectal adenocarcinoma (DLD-1) with a colorimetric assay based on the reduction of MTT reagent (methy-134-thiazolyltetrazolium). The assays show that some concentrations of bare UCNPs were cytotoxic for cervical adenocarcinoma cells (HeLa); however, for human colorectal adenocarcinoma all UCNPs are non-cytotoxic. After UCNPs functionalization with silica-aminosilane (APTES/TEOS), all of the nanoparticles tested were found to be non-cytotoxic for both cell lines. The UCNPs functionalized in this work can be further conjugated with specific ligands and used as biolabels for detection of cancer cells. SAGE Publications 2016-01-01 /pmc/articles/PMC5998266/ /pubmed/29942376 http://dx.doi.org/10.5772/62252 Text en © 2016 Author(s). Licensee InTech. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Nanobiomedicine
Chavez, Dalia Holanda
Juarez-Moreno, Karla
Hirata, Gustavo Alonso
Aminosilane Functionalization and Cytotoxicity Effects of Upconversion Nanoparticles Y(2)O(3) and Gd(2)O(3) Co-Doped with Yb(3+)and Er(3+)
title Aminosilane Functionalization and Cytotoxicity Effects of Upconversion Nanoparticles Y(2)O(3) and Gd(2)O(3) Co-Doped with Yb(3+)and Er(3+)
title_full Aminosilane Functionalization and Cytotoxicity Effects of Upconversion Nanoparticles Y(2)O(3) and Gd(2)O(3) Co-Doped with Yb(3+)and Er(3+)
title_fullStr Aminosilane Functionalization and Cytotoxicity Effects of Upconversion Nanoparticles Y(2)O(3) and Gd(2)O(3) Co-Doped with Yb(3+)and Er(3+)
title_full_unstemmed Aminosilane Functionalization and Cytotoxicity Effects of Upconversion Nanoparticles Y(2)O(3) and Gd(2)O(3) Co-Doped with Yb(3+)and Er(3+)
title_short Aminosilane Functionalization and Cytotoxicity Effects of Upconversion Nanoparticles Y(2)O(3) and Gd(2)O(3) Co-Doped with Yb(3+)and Er(3+)
title_sort aminosilane functionalization and cytotoxicity effects of upconversion nanoparticles y(2)o(3) and gd(2)o(3) co-doped with yb(3+)and er(3+)
topic Nanobiomedicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998266/
https://www.ncbi.nlm.nih.gov/pubmed/29942376
http://dx.doi.org/10.5772/62252
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