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Laser Ablated Albumin Functionalized Spherical Gold Nanoparticles Indicated for Stem Cell Tracking
Cell tracking in cell-based therapy applications helps distinguish cell participation among paracrine effect, neovascularization, and matrix deposition. This preliminary study examined the cellular uptake of gold nanoparticles (AuNPs), observing cytotoxicity and uptake of different sizes and AuNPs c...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9919444/ https://www.ncbi.nlm.nih.gov/pubmed/36770041 http://dx.doi.org/10.3390/ma16031034 |
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author | Dziedzic, Dilcele Silva Moreira Mogharbel, Bassam Felipe Irioda, Ana Carolina Stricker, Priscila Elias Ferreira Woiski, Thiago Demetrius Machado, Thiago Neves Bezerra Jr, Arandi Ginane Athayde Teixeira de Carvalho, Katherine |
author_facet | Dziedzic, Dilcele Silva Moreira Mogharbel, Bassam Felipe Irioda, Ana Carolina Stricker, Priscila Elias Ferreira Woiski, Thiago Demetrius Machado, Thiago Neves Bezerra Jr, Arandi Ginane Athayde Teixeira de Carvalho, Katherine |
author_sort | Dziedzic, Dilcele Silva Moreira |
collection | PubMed |
description | Cell tracking in cell-based therapy applications helps distinguish cell participation among paracrine effect, neovascularization, and matrix deposition. This preliminary study examined the cellular uptake of gold nanoparticles (AuNPs), observing cytotoxicity and uptake of different sizes and AuNPs concentrations in Adipose-derived stromal cells (ASCs). ASCs were incubated for 24 h with Laser ablated Albumin functionalized spherical AuNPs (LA-AuNPs), with average sizes of 2 nm and 53 nm in diameter, in four concentrations, 127 µM, 84 µM, 42 µM, and 23 µM. Cytotoxicity was examined by Live/Dead assay, and erythrocyte hemolysis, and the effect on the cytoskeleton was investigated by immunocytochemistry for β-actin. The LA-AuNPs were internalized by the ASCs in a size and concentration-dependent manner. Clusters were observed as dispersed small ones in the cytosol, and as a sizeable perinuclear cluster, without significant harmful effects on the cells for up to 2 weeks. The Live/Dead and hemolysis percentage results complemented the observations that the larger 53 nm LA-AuNPs in the highest concentrated solution significantly lowered cell viability. The demonstrated safety, cellular uptake, and labelling persistency with LA-AuNPs, synthesized without the combination of chemical solutions, support their use for cell tracking in tissue engineering applications. |
format | Online Article Text |
id | pubmed-9919444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99194442023-02-12 Laser Ablated Albumin Functionalized Spherical Gold Nanoparticles Indicated for Stem Cell Tracking Dziedzic, Dilcele Silva Moreira Mogharbel, Bassam Felipe Irioda, Ana Carolina Stricker, Priscila Elias Ferreira Woiski, Thiago Demetrius Machado, Thiago Neves Bezerra Jr, Arandi Ginane Athayde Teixeira de Carvalho, Katherine Materials (Basel) Article Cell tracking in cell-based therapy applications helps distinguish cell participation among paracrine effect, neovascularization, and matrix deposition. This preliminary study examined the cellular uptake of gold nanoparticles (AuNPs), observing cytotoxicity and uptake of different sizes and AuNPs concentrations in Adipose-derived stromal cells (ASCs). ASCs were incubated for 24 h with Laser ablated Albumin functionalized spherical AuNPs (LA-AuNPs), with average sizes of 2 nm and 53 nm in diameter, in four concentrations, 127 µM, 84 µM, 42 µM, and 23 µM. Cytotoxicity was examined by Live/Dead assay, and erythrocyte hemolysis, and the effect on the cytoskeleton was investigated by immunocytochemistry for β-actin. The LA-AuNPs were internalized by the ASCs in a size and concentration-dependent manner. Clusters were observed as dispersed small ones in the cytosol, and as a sizeable perinuclear cluster, without significant harmful effects on the cells for up to 2 weeks. The Live/Dead and hemolysis percentage results complemented the observations that the larger 53 nm LA-AuNPs in the highest concentrated solution significantly lowered cell viability. The demonstrated safety, cellular uptake, and labelling persistency with LA-AuNPs, synthesized without the combination of chemical solutions, support their use for cell tracking in tissue engineering applications. MDPI 2023-01-24 /pmc/articles/PMC9919444/ /pubmed/36770041 http://dx.doi.org/10.3390/ma16031034 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Dziedzic, Dilcele Silva Moreira Mogharbel, Bassam Felipe Irioda, Ana Carolina Stricker, Priscila Elias Ferreira Woiski, Thiago Demetrius Machado, Thiago Neves Bezerra Jr, Arandi Ginane Athayde Teixeira de Carvalho, Katherine Laser Ablated Albumin Functionalized Spherical Gold Nanoparticles Indicated for Stem Cell Tracking |
title | Laser Ablated Albumin Functionalized Spherical Gold Nanoparticles Indicated for Stem Cell Tracking |
title_full | Laser Ablated Albumin Functionalized Spherical Gold Nanoparticles Indicated for Stem Cell Tracking |
title_fullStr | Laser Ablated Albumin Functionalized Spherical Gold Nanoparticles Indicated for Stem Cell Tracking |
title_full_unstemmed | Laser Ablated Albumin Functionalized Spherical Gold Nanoparticles Indicated for Stem Cell Tracking |
title_short | Laser Ablated Albumin Functionalized Spherical Gold Nanoparticles Indicated for Stem Cell Tracking |
title_sort | laser ablated albumin functionalized spherical gold nanoparticles indicated for stem cell tracking |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9919444/ https://www.ncbi.nlm.nih.gov/pubmed/36770041 http://dx.doi.org/10.3390/ma16031034 |
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