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Formulation of novel lipid-coated magnetic nanoparticles as the probe for in vivo imaging

BACKGROUND: Application of superparamagnetic iron oxide nanoparticles (SPIOs) as the contrast agent has improved the quality of magnetic resonance (MR) imaging. Low efficiency of loading the commercially available iron oxide nanoparticles into cells and the cytotoxicity of previously formulated comp...

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Autores principales: Huang, Huey-Chung, Chang, Po-Yuan, Chang, Karen, Chen, Chao-Yu, Lin, Chung-Wu, Chen, Jyh-Horng, Mou, Chung-Yuan, Chang, Zee-Fen, Chang, Fu-Hsiung
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758848/
https://www.ncbi.nlm.nih.gov/pubmed/19772552
http://dx.doi.org/10.1186/1423-0127-16-86
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author Huang, Huey-Chung
Chang, Po-Yuan
Chang, Karen
Chen, Chao-Yu
Lin, Chung-Wu
Chen, Jyh-Horng
Mou, Chung-Yuan
Chang, Zee-Fen
Chang, Fu-Hsiung
author_facet Huang, Huey-Chung
Chang, Po-Yuan
Chang, Karen
Chen, Chao-Yu
Lin, Chung-Wu
Chen, Jyh-Horng
Mou, Chung-Yuan
Chang, Zee-Fen
Chang, Fu-Hsiung
author_sort Huang, Huey-Chung
collection PubMed
description BACKGROUND: Application of superparamagnetic iron oxide nanoparticles (SPIOs) as the contrast agent has improved the quality of magnetic resonance (MR) imaging. Low efficiency of loading the commercially available iron oxide nanoparticles into cells and the cytotoxicity of previously formulated complexes limit their usage as the image probe. Here, we formulated new cationic lipid nanoparticles containing SPIOs feasible for in vivo imaging. METHODS: Hydrophobic SPIOs were incorporated into cationic lipid 1,2-dioleoyl-3-(trimethylammonium) propane (DOTAP) and polyethylene-glycol-2000-1,2-distearyl-3-sn-phosphatidylethanolamine (PEG-DSPE) based micelles by self-assembly procedure to form lipid-coated SPIOs (L-SPIOs). Trace amount of Rhodamine-dioleoyl-phosphatidylethanolamine (Rhodamine-DOPE) was added as a fluorescent indicator. Particle size and zeta potential of L-SPIOs were determined by Dynamic Light Scattering (DLS) and Laser Doppler Velocimetry (LDV), respectively. HeLa, PC-3 and Neuro-2a cells were tested for loading efficiency and cytotoxicity of L-SPIOs using fluorescent microscopy, Prussian blue staining and flow cytometry. L-SPIO-loaded CT-26 cells were tested for in vivo MR imaging. RESULTS: The novel formulation generates L-SPIOs particle with the average size of 46 nm. We showed efficient cellular uptake of these L-SPIOs with cationic surface charge into HeLa, PC-3 and Neuro-2a cells. The L-SPIO-loaded cells exhibited similar growth potential as compared to unloaded cells, and could be sorted by a magnet stand over ten-day duration. Furthermore, when SPIO-loaded CT-26 tumor cells were injected into Balb/c mice, the growth status of these tumor cells could be monitored using optical and MR images. CONCLUSION: We have developed a novel cationic lipid-based nanoparticle of SPIOs with high loading efficiency, low cytotoxicity and long-term imaging signals. The results suggested these newly formulated non-toxic lipid-coated magnetic nanoparticles as a versatile image probe for cell tracking.
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spelling pubmed-27588482009-10-08 Formulation of novel lipid-coated magnetic nanoparticles as the probe for in vivo imaging Huang, Huey-Chung Chang, Po-Yuan Chang, Karen Chen, Chao-Yu Lin, Chung-Wu Chen, Jyh-Horng Mou, Chung-Yuan Chang, Zee-Fen Chang, Fu-Hsiung J Biomed Sci Research BACKGROUND: Application of superparamagnetic iron oxide nanoparticles (SPIOs) as the contrast agent has improved the quality of magnetic resonance (MR) imaging. Low efficiency of loading the commercially available iron oxide nanoparticles into cells and the cytotoxicity of previously formulated complexes limit their usage as the image probe. Here, we formulated new cationic lipid nanoparticles containing SPIOs feasible for in vivo imaging. METHODS: Hydrophobic SPIOs were incorporated into cationic lipid 1,2-dioleoyl-3-(trimethylammonium) propane (DOTAP) and polyethylene-glycol-2000-1,2-distearyl-3-sn-phosphatidylethanolamine (PEG-DSPE) based micelles by self-assembly procedure to form lipid-coated SPIOs (L-SPIOs). Trace amount of Rhodamine-dioleoyl-phosphatidylethanolamine (Rhodamine-DOPE) was added as a fluorescent indicator. Particle size and zeta potential of L-SPIOs were determined by Dynamic Light Scattering (DLS) and Laser Doppler Velocimetry (LDV), respectively. HeLa, PC-3 and Neuro-2a cells were tested for loading efficiency and cytotoxicity of L-SPIOs using fluorescent microscopy, Prussian blue staining and flow cytometry. L-SPIO-loaded CT-26 cells were tested for in vivo MR imaging. RESULTS: The novel formulation generates L-SPIOs particle with the average size of 46 nm. We showed efficient cellular uptake of these L-SPIOs with cationic surface charge into HeLa, PC-3 and Neuro-2a cells. The L-SPIO-loaded cells exhibited similar growth potential as compared to unloaded cells, and could be sorted by a magnet stand over ten-day duration. Furthermore, when SPIO-loaded CT-26 tumor cells were injected into Balb/c mice, the growth status of these tumor cells could be monitored using optical and MR images. CONCLUSION: We have developed a novel cationic lipid-based nanoparticle of SPIOs with high loading efficiency, low cytotoxicity and long-term imaging signals. The results suggested these newly formulated non-toxic lipid-coated magnetic nanoparticles as a versatile image probe for cell tracking. BioMed Central 2009-09-21 /pmc/articles/PMC2758848/ /pubmed/19772552 http://dx.doi.org/10.1186/1423-0127-16-86 Text en Copyright ©2009 Huang et al; licensee BioMed Central Ltd. 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 Research
Huang, Huey-Chung
Chang, Po-Yuan
Chang, Karen
Chen, Chao-Yu
Lin, Chung-Wu
Chen, Jyh-Horng
Mou, Chung-Yuan
Chang, Zee-Fen
Chang, Fu-Hsiung
Formulation of novel lipid-coated magnetic nanoparticles as the probe for in vivo imaging
title Formulation of novel lipid-coated magnetic nanoparticles as the probe for in vivo imaging
title_full Formulation of novel lipid-coated magnetic nanoparticles as the probe for in vivo imaging
title_fullStr Formulation of novel lipid-coated magnetic nanoparticles as the probe for in vivo imaging
title_full_unstemmed Formulation of novel lipid-coated magnetic nanoparticles as the probe for in vivo imaging
title_short Formulation of novel lipid-coated magnetic nanoparticles as the probe for in vivo imaging
title_sort formulation of novel lipid-coated magnetic nanoparticles as the probe for in vivo imaging
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758848/
https://www.ncbi.nlm.nih.gov/pubmed/19772552
http://dx.doi.org/10.1186/1423-0127-16-86
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