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Synthesis of ginsenoside Re-based carbon dots applied for bioimaging and effective inhibition of cancer cells

BACKGROUND: Fluorescent carbon-based nanomaterials have promising properties such as biosensing, cell imaging, tracing and drug delivery. However, carbon dots (CDs) with specific inherent biological functions have not been investigated. Ginsenosides are the components with multiple bioactivities fou...

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Autores principales: Yao, Hua, Li, Jing, Song, Yubin, Zhao, Hong, Wei, Zhenhong, Li, Xiuying, Jin, Yongri, Yang, Bai, Jiang, Jinlan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6188153/
https://www.ncbi.nlm.nih.gov/pubmed/30349248
http://dx.doi.org/10.2147/IJN.S176176
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author Yao, Hua
Li, Jing
Song, Yubin
Zhao, Hong
Wei, Zhenhong
Li, Xiuying
Jin, Yongri
Yang, Bai
Jiang, Jinlan
author_facet Yao, Hua
Li, Jing
Song, Yubin
Zhao, Hong
Wei, Zhenhong
Li, Xiuying
Jin, Yongri
Yang, Bai
Jiang, Jinlan
author_sort Yao, Hua
collection PubMed
description BACKGROUND: Fluorescent carbon-based nanomaterials have promising properties such as biosensing, cell imaging, tracing and drug delivery. However, carbon dots (CDs) with specific inherent biological functions have not been investigated. Ginsenosides are the components with multiple bioactivities found in plants of the genus Panax, which have attracted a lot of attention for their anticancer effect. MATERIALS AND METHODS: In this study, we prepared a kind of novel photoluminescent CDs from ginsenoside Re by one-step hydrothermal synthesis method. The conventional methods including transmission electron microscopy, Fourier transform infrared spectroscopy, HPLC and fluorescence spectrum were used for characterization of CDs. In vitro anticancer effect was investigated by cytotoxicity assay, flow cytometry and Western blot analysis. RESULTS: The as-prepared Re-CDs had an average diameter of 4.6±0.6 nm and excellent luminescent properties. Cellular uptake of Re-CDs was facilitated by their tiny nanosize, with evidence of their bright excitation-dependent fluorescent images. Compared with ginsenoside Re, the Re-CDs showed greater inhibition efficiency of cancer cell proliferation, with lower toxicity to the normal cells. The anticancer activity of Re-CDs was suggested to be associated with the generation of large amount of ROS and the caspase-3 related cell apoptosis. CONCLUSION: Hopefully, the dual functional Re-CDs, which could both exhibit bioimaging and anticancer effect, are expected to have great potential in future clinical applications.
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spelling pubmed-61881532018-10-22 Synthesis of ginsenoside Re-based carbon dots applied for bioimaging and effective inhibition of cancer cells Yao, Hua Li, Jing Song, Yubin Zhao, Hong Wei, Zhenhong Li, Xiuying Jin, Yongri Yang, Bai Jiang, Jinlan Int J Nanomedicine Original Research BACKGROUND: Fluorescent carbon-based nanomaterials have promising properties such as biosensing, cell imaging, tracing and drug delivery. However, carbon dots (CDs) with specific inherent biological functions have not been investigated. Ginsenosides are the components with multiple bioactivities found in plants of the genus Panax, which have attracted a lot of attention for their anticancer effect. MATERIALS AND METHODS: In this study, we prepared a kind of novel photoluminescent CDs from ginsenoside Re by one-step hydrothermal synthesis method. The conventional methods including transmission electron microscopy, Fourier transform infrared spectroscopy, HPLC and fluorescence spectrum were used for characterization of CDs. In vitro anticancer effect was investigated by cytotoxicity assay, flow cytometry and Western blot analysis. RESULTS: The as-prepared Re-CDs had an average diameter of 4.6±0.6 nm and excellent luminescent properties. Cellular uptake of Re-CDs was facilitated by their tiny nanosize, with evidence of their bright excitation-dependent fluorescent images. Compared with ginsenoside Re, the Re-CDs showed greater inhibition efficiency of cancer cell proliferation, with lower toxicity to the normal cells. The anticancer activity of Re-CDs was suggested to be associated with the generation of large amount of ROS and the caspase-3 related cell apoptosis. CONCLUSION: Hopefully, the dual functional Re-CDs, which could both exhibit bioimaging and anticancer effect, are expected to have great potential in future clinical applications. Dove Medical Press 2018-10-09 /pmc/articles/PMC6188153/ /pubmed/30349248 http://dx.doi.org/10.2147/IJN.S176176 Text en © 2018 Yao et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Yao, Hua
Li, Jing
Song, Yubin
Zhao, Hong
Wei, Zhenhong
Li, Xiuying
Jin, Yongri
Yang, Bai
Jiang, Jinlan
Synthesis of ginsenoside Re-based carbon dots applied for bioimaging and effective inhibition of cancer cells
title Synthesis of ginsenoside Re-based carbon dots applied for bioimaging and effective inhibition of cancer cells
title_full Synthesis of ginsenoside Re-based carbon dots applied for bioimaging and effective inhibition of cancer cells
title_fullStr Synthesis of ginsenoside Re-based carbon dots applied for bioimaging and effective inhibition of cancer cells
title_full_unstemmed Synthesis of ginsenoside Re-based carbon dots applied for bioimaging and effective inhibition of cancer cells
title_short Synthesis of ginsenoside Re-based carbon dots applied for bioimaging and effective inhibition of cancer cells
title_sort synthesis of ginsenoside re-based carbon dots applied for bioimaging and effective inhibition of cancer cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6188153/
https://www.ncbi.nlm.nih.gov/pubmed/30349248
http://dx.doi.org/10.2147/IJN.S176176
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