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Anti-cancer efficacy of biotinylated chitosan nanoparticles in liver cancer

The present study investigated the synthesis of biotinylated chitosan (Bio-CS) from chitosan using a nanomaterial skeleton with biotin and the successful targeting of the formulation in liver cancer cells. Bio-CS was validated by fourier transformed infrared spectroscopy and hydrogen(-1) nuclear mag...

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Autores principales: Cheng, Mingrong, Zhu, Weiping, Li, Qing, Dai, Dejian, Hou, Yiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601715/
https://www.ncbi.nlm.nih.gov/pubmed/28938619
http://dx.doi.org/10.18632/oncotarget.19146
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author Cheng, Mingrong
Zhu, Weiping
Li, Qing
Dai, Dejian
Hou, Yiming
author_facet Cheng, Mingrong
Zhu, Weiping
Li, Qing
Dai, Dejian
Hou, Yiming
author_sort Cheng, Mingrong
collection PubMed
description The present study investigated the synthesis of biotinylated chitosan (Bio-CS) from chitosan using a nanomaterial skeleton with biotin and the successful targeting of the formulation in liver cancer cells. Bio-CS was validated by fourier transformed infrared spectroscopy and hydrogen(-1) nuclear magnetic resonance spectroscopy. Bio-CS and plasmid DNA were used to construct Bio-CS/plasmid DNA nanoparticles according to the optimal molar ratio of 1:1 and the optimal pH-value of 5.5. Under these conditions, the parameters mean particle size, potential, encapsulation rate and drug loading, were 82.9 nm, +21.8 mV, 85.7% and 35.4%, respectively. Bio-CS exhibited an apparent liver cancer targeting effect in vitro and in vivo, as demonstrated by confocal laser scanning, green fluorescent protein transfection, and in vivo imaging assays. In addition, the Bio-CS/plasmid DNA nanoparticles significantly increased the survival period of the orthotropic liver cancer mouse model compared with the plasmid DNA, with no apparent side effects on the cells. Bio-CS nanomaterials stimulated an immune response in hepatoma cells via increased expression of GM-CSF, IL-21 and Rae-1 markers. The data suggest that Bio-CS increased the inhibition of liver cancer cell proliferation in vitro and the activation of the cellular immunity in vivo.
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spelling pubmed-56017152017-09-21 Anti-cancer efficacy of biotinylated chitosan nanoparticles in liver cancer Cheng, Mingrong Zhu, Weiping Li, Qing Dai, Dejian Hou, Yiming Oncotarget Research Paper The present study investigated the synthesis of biotinylated chitosan (Bio-CS) from chitosan using a nanomaterial skeleton with biotin and the successful targeting of the formulation in liver cancer cells. Bio-CS was validated by fourier transformed infrared spectroscopy and hydrogen(-1) nuclear magnetic resonance spectroscopy. Bio-CS and plasmid DNA were used to construct Bio-CS/plasmid DNA nanoparticles according to the optimal molar ratio of 1:1 and the optimal pH-value of 5.5. Under these conditions, the parameters mean particle size, potential, encapsulation rate and drug loading, were 82.9 nm, +21.8 mV, 85.7% and 35.4%, respectively. Bio-CS exhibited an apparent liver cancer targeting effect in vitro and in vivo, as demonstrated by confocal laser scanning, green fluorescent protein transfection, and in vivo imaging assays. In addition, the Bio-CS/plasmid DNA nanoparticles significantly increased the survival period of the orthotropic liver cancer mouse model compared with the plasmid DNA, with no apparent side effects on the cells. Bio-CS nanomaterials stimulated an immune response in hepatoma cells via increased expression of GM-CSF, IL-21 and Rae-1 markers. The data suggest that Bio-CS increased the inhibition of liver cancer cell proliferation in vitro and the activation of the cellular immunity in vivo. Impact Journals LLC 2017-07-10 /pmc/articles/PMC5601715/ /pubmed/28938619 http://dx.doi.org/10.18632/oncotarget.19146 Text en Copyright: © 2017 Cheng et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Cheng, Mingrong
Zhu, Weiping
Li, Qing
Dai, Dejian
Hou, Yiming
Anti-cancer efficacy of biotinylated chitosan nanoparticles in liver cancer
title Anti-cancer efficacy of biotinylated chitosan nanoparticles in liver cancer
title_full Anti-cancer efficacy of biotinylated chitosan nanoparticles in liver cancer
title_fullStr Anti-cancer efficacy of biotinylated chitosan nanoparticles in liver cancer
title_full_unstemmed Anti-cancer efficacy of biotinylated chitosan nanoparticles in liver cancer
title_short Anti-cancer efficacy of biotinylated chitosan nanoparticles in liver cancer
title_sort anti-cancer efficacy of biotinylated chitosan nanoparticles in liver cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601715/
https://www.ncbi.nlm.nih.gov/pubmed/28938619
http://dx.doi.org/10.18632/oncotarget.19146
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