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Cytotoxicity of InP/ZnS Quantum Dots With Different Surface Functional Groups Toward Two Lung-Derived Cell Lines

Although InP/ZnS quantum dots (QDs) have emerged as a presumably less hazardous alternative to cadmium-based QDs, their toxicity has not been fully understood. In this work, we report the cytotoxicity of InP/ZnS QDs with different surface groups (NH(2), COOH, OH) toward two lung-derived cell lines....

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Autores principales: Chen, Ting, Li, Li, Xu, Gaixia, Wang, Xiaomei, Wang, Jie, Chen, Yajing, Jiang, Wenxiao, Yang, Zhiwen, Lin, Guimiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053512/
https://www.ncbi.nlm.nih.gov/pubmed/30057549
http://dx.doi.org/10.3389/fphar.2018.00763
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author Chen, Ting
Li, Li
Xu, Gaixia
Wang, Xiaomei
Wang, Jie
Chen, Yajing
Jiang, Wenxiao
Yang, Zhiwen
Lin, Guimiao
author_facet Chen, Ting
Li, Li
Xu, Gaixia
Wang, Xiaomei
Wang, Jie
Chen, Yajing
Jiang, Wenxiao
Yang, Zhiwen
Lin, Guimiao
author_sort Chen, Ting
collection PubMed
description Although InP/ZnS quantum dots (QDs) have emerged as a presumably less hazardous alternative to cadmium-based QDs, their toxicity has not been fully understood. In this work, we report the cytotoxicity of InP/ZnS QDs with different surface groups (NH(2), COOH, OH) toward two lung-derived cell lines. The diameter and the spectra of InP/ZnS QDs were characterized and the hydrodynamic size of QDs in aqueous solution was compared. The confocal laser scanning microscopy was applied to visualize the labeling of QDs for human lung cancer cell HCC-15 and Alveolar type II epithelial cell RLE-6TN. The flow cytometry was used to confirm qualitatively the uptake efficiency of QDs, the cell apoptosis and ROS generation, respectively. The results showed that in deionized water, InP/ZnS-OH QDs were easier to aggregate, and the hydrodynamic size was much greater than the other InP/ZnS QDs. All these InP/ZnS QDs were able to enter the cells, with higher uptake efficiency for InP/ZnS-COOH and InP/ZnS-NH(2) at low concentration. High doses of InP/ZnS QDs caused the cell viability to decrease, and InP/ZnS-COOH QDs and InP/ZnS-NH(2) QDs appeared to be more toxic than InP/ZnS-OH QDs. In addition, all these InP/ZnS QDs promoted cell apoptosis and intracellular ROS generation after co-cultured with cells. These results suggested that appropriate concentration and surface functional groups should be optimized when InP/ZnS QDs are utilized for biological imaging and therapeutic purpose in the future.
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spelling pubmed-60535122018-07-27 Cytotoxicity of InP/ZnS Quantum Dots With Different Surface Functional Groups Toward Two Lung-Derived Cell Lines Chen, Ting Li, Li Xu, Gaixia Wang, Xiaomei Wang, Jie Chen, Yajing Jiang, Wenxiao Yang, Zhiwen Lin, Guimiao Front Pharmacol Pharmacology Although InP/ZnS quantum dots (QDs) have emerged as a presumably less hazardous alternative to cadmium-based QDs, their toxicity has not been fully understood. In this work, we report the cytotoxicity of InP/ZnS QDs with different surface groups (NH(2), COOH, OH) toward two lung-derived cell lines. The diameter and the spectra of InP/ZnS QDs were characterized and the hydrodynamic size of QDs in aqueous solution was compared. The confocal laser scanning microscopy was applied to visualize the labeling of QDs for human lung cancer cell HCC-15 and Alveolar type II epithelial cell RLE-6TN. The flow cytometry was used to confirm qualitatively the uptake efficiency of QDs, the cell apoptosis and ROS generation, respectively. The results showed that in deionized water, InP/ZnS-OH QDs were easier to aggregate, and the hydrodynamic size was much greater than the other InP/ZnS QDs. All these InP/ZnS QDs were able to enter the cells, with higher uptake efficiency for InP/ZnS-COOH and InP/ZnS-NH(2) at low concentration. High doses of InP/ZnS QDs caused the cell viability to decrease, and InP/ZnS-COOH QDs and InP/ZnS-NH(2) QDs appeared to be more toxic than InP/ZnS-OH QDs. In addition, all these InP/ZnS QDs promoted cell apoptosis and intracellular ROS generation after co-cultured with cells. These results suggested that appropriate concentration and surface functional groups should be optimized when InP/ZnS QDs are utilized for biological imaging and therapeutic purpose in the future. Frontiers Media S.A. 2018-07-13 /pmc/articles/PMC6053512/ /pubmed/30057549 http://dx.doi.org/10.3389/fphar.2018.00763 Text en Copyright © 2018 Chen, Li, Xu, Wang, Wang, Chen, Jiang, Yang and Lin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Chen, Ting
Li, Li
Xu, Gaixia
Wang, Xiaomei
Wang, Jie
Chen, Yajing
Jiang, Wenxiao
Yang, Zhiwen
Lin, Guimiao
Cytotoxicity of InP/ZnS Quantum Dots With Different Surface Functional Groups Toward Two Lung-Derived Cell Lines
title Cytotoxicity of InP/ZnS Quantum Dots With Different Surface Functional Groups Toward Two Lung-Derived Cell Lines
title_full Cytotoxicity of InP/ZnS Quantum Dots With Different Surface Functional Groups Toward Two Lung-Derived Cell Lines
title_fullStr Cytotoxicity of InP/ZnS Quantum Dots With Different Surface Functional Groups Toward Two Lung-Derived Cell Lines
title_full_unstemmed Cytotoxicity of InP/ZnS Quantum Dots With Different Surface Functional Groups Toward Two Lung-Derived Cell Lines
title_short Cytotoxicity of InP/ZnS Quantum Dots With Different Surface Functional Groups Toward Two Lung-Derived Cell Lines
title_sort cytotoxicity of inp/zns quantum dots with different surface functional groups toward two lung-derived cell lines
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053512/
https://www.ncbi.nlm.nih.gov/pubmed/30057549
http://dx.doi.org/10.3389/fphar.2018.00763
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