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Biocompatibility of hydrophilic silica-coated CdTe quantum dots and magnetic nanoparticles

Fluorescent magnetic nanoparticles exhibit great application prospects in biomedical engineering. Herein, we reported the effects of hydrophilic silica-coated CdTe quantum dots and magnetic nanoparticles (FMNPs) on human embryonic kidney 293 (HEK293) cells and mice with the aim of investigating thei...

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Autores principales: Ruan, Jing, Wang, Kan, Song, Hua, Xu, Xin, Ji, Jiajia, Cui, Daxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3211365/
https://www.ncbi.nlm.nih.gov/pubmed/21711857
http://dx.doi.org/10.1186/1556-276X-6-299
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author Ruan, Jing
Wang, Kan
Song, Hua
Xu, Xin
Ji, Jiajia
Cui, Daxiang
author_facet Ruan, Jing
Wang, Kan
Song, Hua
Xu, Xin
Ji, Jiajia
Cui, Daxiang
author_sort Ruan, Jing
collection PubMed
description Fluorescent magnetic nanoparticles exhibit great application prospects in biomedical engineering. Herein, we reported the effects of hydrophilic silica-coated CdTe quantum dots and magnetic nanoparticles (FMNPs) on human embryonic kidney 293 (HEK293) cells and mice with the aim of investigating their biocompatibility. FMNPs with 150 nm in diameter were prepared, and characterized by high-resolution transmission electron microscopy and photoluminescence (PL) spectra and magnetometer. HEK293 cells were cultured with different doses of FMNPs (20, 50, and 100μ g/ml) for 1-4 days. Cell viability and adhesion ability were analyzed by CCK8 method and Western blotting. 30 mice were randomly divided into three groups, and were, respectively, injected via tail vein with 20, 60, and 100 μg FMNPs, and then were, respectively, raised for 1, 7, and 30 days, then their lifespan, important organs, and blood biochemical parameters were analyzed. Results show that the prepared water-soluble FMNPs had high fluorescent and magnetic properties, less than 50 μg/ml of FMNPs exhibited good biocompatibility to HEK293 cells, the cell viability, and adhesion ability were similar to the control HEK293 cells. FMNPs primarily accumulated in those organs such as lung, liver, and spleen. Lung exposed to FMNPs displayed a dose-dependent inflammatory response, blood biochemical parameters such as white blood cell count (WBC), alanine aminotransferase (ALT), and aspartate aminotransferase (AST), displayed significant increase when the FMNPs were injected into mice at dose of 100μg. In conclusion, FMNPs exhibit good biocompatibility to cells under the dose of less than 50 μg/ml, and to mice under the dose of less than 2mg/kg body weight. The FMNPs' biocompatibility must be considered when FMNPs are used for in vivo diagnosis and therapy.
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spelling pubmed-32113652011-11-09 Biocompatibility of hydrophilic silica-coated CdTe quantum dots and magnetic nanoparticles Ruan, Jing Wang, Kan Song, Hua Xu, Xin Ji, Jiajia Cui, Daxiang Nanoscale Res Lett Nano Express Fluorescent magnetic nanoparticles exhibit great application prospects in biomedical engineering. Herein, we reported the effects of hydrophilic silica-coated CdTe quantum dots and magnetic nanoparticles (FMNPs) on human embryonic kidney 293 (HEK293) cells and mice with the aim of investigating their biocompatibility. FMNPs with 150 nm in diameter were prepared, and characterized by high-resolution transmission electron microscopy and photoluminescence (PL) spectra and magnetometer. HEK293 cells were cultured with different doses of FMNPs (20, 50, and 100μ g/ml) for 1-4 days. Cell viability and adhesion ability were analyzed by CCK8 method and Western blotting. 30 mice were randomly divided into three groups, and were, respectively, injected via tail vein with 20, 60, and 100 μg FMNPs, and then were, respectively, raised for 1, 7, and 30 days, then their lifespan, important organs, and blood biochemical parameters were analyzed. Results show that the prepared water-soluble FMNPs had high fluorescent and magnetic properties, less than 50 μg/ml of FMNPs exhibited good biocompatibility to HEK293 cells, the cell viability, and adhesion ability were similar to the control HEK293 cells. FMNPs primarily accumulated in those organs such as lung, liver, and spleen. Lung exposed to FMNPs displayed a dose-dependent inflammatory response, blood biochemical parameters such as white blood cell count (WBC), alanine aminotransferase (ALT), and aspartate aminotransferase (AST), displayed significant increase when the FMNPs were injected into mice at dose of 100μg. In conclusion, FMNPs exhibit good biocompatibility to cells under the dose of less than 50 μg/ml, and to mice under the dose of less than 2mg/kg body weight. The FMNPs' biocompatibility must be considered when FMNPs are used for in vivo diagnosis and therapy. Springer 2011-04-06 /pmc/articles/PMC3211365/ /pubmed/21711857 http://dx.doi.org/10.1186/1556-276X-6-299 Text en Copyright ©2011 Ruan et al; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Nano Express
Ruan, Jing
Wang, Kan
Song, Hua
Xu, Xin
Ji, Jiajia
Cui, Daxiang
Biocompatibility of hydrophilic silica-coated CdTe quantum dots and magnetic nanoparticles
title Biocompatibility of hydrophilic silica-coated CdTe quantum dots and magnetic nanoparticles
title_full Biocompatibility of hydrophilic silica-coated CdTe quantum dots and magnetic nanoparticles
title_fullStr Biocompatibility of hydrophilic silica-coated CdTe quantum dots and magnetic nanoparticles
title_full_unstemmed Biocompatibility of hydrophilic silica-coated CdTe quantum dots and magnetic nanoparticles
title_short Biocompatibility of hydrophilic silica-coated CdTe quantum dots and magnetic nanoparticles
title_sort biocompatibility of hydrophilic silica-coated cdte quantum dots and magnetic nanoparticles
topic Nano Express
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3211365/
https://www.ncbi.nlm.nih.gov/pubmed/21711857
http://dx.doi.org/10.1186/1556-276X-6-299
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