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On the Cyto‐Toxicity Caused by Quantum Dots
Abstract
Quantum dots (QDs) such as CdSe QDs have been introduced as new fluorophores. The QDs conjugated with antibody are starting to be widely used for immunostaining. However there is still not sufficient analysis of the toxicity of QDs in the literature. Therefore we evaluated the cell damage caused by the quantum dots for biological applications. We performed cell viability assay to determine the difference in cell damage depending on the sizes and colors of mercapto‐undecanoic acid (MUA) QDs and the cell types. The results showed that the cell viability decreased with increasing concentration of MUA‐QDs. But in the case of Vero cell (African green monkey's kidney cell) with red fluorescence QD (QD640), the cell damage was less than for the others. Furthermore through the flow cytometry assay we found that this cell damage caused by MUA‐QD turned out to be cell death after 4‐6‐hr incubation. From the two assays described above, we found that there is a range of concentration of MUA‐QDs where the cell viability decreased without cell death occurring and thus we conclude that attention should be given when MUA‐QDs are applied to living organisms even in low concentrations.
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“Although the potential of quantum dots to be harmful has been rather controversially discussed (12,13), the effect of”
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Applications of quantum dots in Food Science and biology
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Self-citationFerritin: A Promising Nanoreactor and Nanocarrier for Bionanotechnology
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“However, it has been shown that surface modifications can modulate the biocompatibility of QDs used in certain applications (Shiohara et al., 2004; Kirchner et al., 2005).”
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“39–41 A subsequent study demonstrated that quantum dot toxicity was reduced after surface modification with N-acetylcysteine, while the nonmodified quantum dots induced lipid peroxidation in the cells.”
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“tested the QDs sensitivity to different cell lines and demonstrated that cytotoxicity was dependent on the cell type exposed [19].”
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Metadata
- Authors
- Shiohara, A., Hoshino, A., Hanaki, K., Suzuki, K., & Yamamoto, K.
- Affiliations
- National Institute of Infectious Diseases (JP)
- Department of Medical Ecology and Informatics, Research Institute International Medical Center of Japan Shinjuku‐ku Tokyo 162‐8655 Japan
- Corresponding author
- Yamamoto, Kenji
- Venue
- Microbiology and Immunology
- Publisher
- Wiley
- Published
- 2004-09
- Volume
- 48
- Issue
- 9
- Pages
- 669-675
- ISSN
- 0385-5600 (ISSN-L)
- 1348-0421
- OpenAlex
- W2050289957
- Semantic Scholar
- ed1ee35465dc4e717235d9a635cb06e15cacd4ce
- Cited by
- 385
- References
- 31
- Citations by year
- 2026: 4 · 2025: 2 · 2024: 9 · 2023: 12 · 2022: 6 · 2021: 10 · 2020: 14 · 2019: 10 · 2018: 12 · 2017: 17 · 2016: 15 · 2015: 22 · 2014: 21 · 2013: 18 · 2012: 28
- FWCI
- 12.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Microbiology and Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Physical Sciences › Materials Science › Materials Chemistry › Quantum Dots Synthesis And Properties
- Physical Sciences › Materials Science › Materials Chemistry › Nanoparticles: synthesis and applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Photodynamic Therapy Research Studies
- Keywords
- quantum dots, cytotoxicity, CdSe quantum dots, cell viability, cell death, Vero cells, immunostaining, nanoparticle toxicity
- MeSH terms
- Animals, Cadmium, Cell Survival, Chlorocebus aethiops, Flow Cytometry, Fluorescent Dyes, HeLa Cells, Humans, Selenium, Sulfhydryl Compounds, Vero Cells, Cell Death, Hepatocytes, Quantum Dots
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