The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Meta-analysis of cellular toxicity for cadmium-containing quantum dots
Abstract
Understanding the relationships between the physicochemical properties of engineered nanomaterials and their toxicity is critical for environmental and health risk analysis. However, this task is confounded by material diversity, heterogeneity of published data and limited sampling within individual studies. Here, we present an approach for analysing and extracting pertinent knowledge from published studies focusing on the cellular toxicity of cadmium-containing semiconductor quantum dots. From 307 publications, we obtain 1,741 cell viability-related data samples, each with 24 qualitative and quantitative attributes describing the material properties and experimental conditions. Using random forest regression models to analyse the data, we show that toxicity is closely correlated with quantum dot surface properties (including shell, ligand and surface modifications), diameter, assay type and exposure time. Our approach of integrating quantitative and categorical data provides a roadmap for interrogating the wide-ranging toxicity data in the literature and suggests that meta-analysis can help develop methods for predicting the toxicity of engineered nanomaterials.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Several literature studies have identified causal relationships between the biological outcomes and important ENMs properties.239”
From QSAR without borders (2020) · cites this paper as [239]
In the citing paper
“Toxicity prediction models trained on these attribute combinations can sometimes identify causal relationships,239 which can be effectively achieved with the Bayesian Network (BN, also called a Bayesian Belief network, BBN) approach.249”
From QSAR without borders (2020) · cites this paper as [239]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Breiman, L. (2001) · Machine Learning · doi:10.1023/a:1010933404324 · Cited by 133,538
Quantifying heterogeneity in a meta‐analysis
Higgins, J. P. T., & Thompson, S. G. (2002) · Statistics in Medicine · doi:10.1002/sim.1186 · Cited by 36,763
Sharifi, S., Behzadi, S., Laurent, S., Laird Forrest, M., Stroeve, P., & Mahmoudi, M. (2012) · Chem. Soc. Rev. · doi:10.1039/c1cs15188f · Cited by 1,460
Brunner, T. J., Wick, P., Manser, P., Spohn, P., Grass, R. N., Limbach, L. K., Bruinink, A., & Stark, W. J. (2006) · Environmental Science & Technology · doi:10.1021/es052069i · Cited by 1,385
On the Cyto‐Toxicity Caused by Quantum Dots
Shiohara, A., Hoshino, A., Hanaki, K., Suzuki, K., & Yamamoto, K. (2004) · Microbiology and Immunology · doi:10.1111/j.1348-0421.2004.tb03478.x · Cited by 385
Ryman-Rasmussen, J. P., Riviere, J. E., & Monteiro-Riviere, N. A. (2007) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700508 · Cited by 357
Biological interactions of quantum dot nanoparticles in skin and in human epidermal keratinocytes
ZHANG, L., YU, W., COLVIN, V, & MONTEIRORIVIERE, N. (2008) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2007.12.022 · Cited by 247
Flagged first, then by citations
Research works printed but not linked: 342
- Colvin, V. L. The potential environmental impact of engineered nanomaterials. Nature Biotechnol. 21, 1166–1170 (2003). · DOI
- Nel, A., Xia, T., Madler, L. & Li, N. Toxic potential of materials at the nanolevel. Science 311, 622–627 (2006). · DOI · Paper page
- Ray, P. C., Yu, H. T. & Fu, P. P. Toxicity and environmental risks of nanomaterials: challenges and future needs. J. Environ. Sci. Health C 27, 1–35 (2009). · DOI
- Kahru, A. & Dubourguier, H. C. From ecotoxicology to nanoecotoxicology. Toxicology 269, 105–119 (2010). · DOI
- Jiang, W., Kim, B. Y. S., Rutka, J. T. & Chan, W. C. W. Nanoparticle-mediated cellular response is size-dependent. Nature Nanotech. 3, 145–150 (2008). · DOI
- Cattaneo, A. G. et al. Nanotechnology and human health: risks and benefits. J. Appl. Toxicol. 30, 730–744 (2010). · DOI
- Brouwer, D. H. Control banding approaches for nanomaterials. Ann. Occup. Hyg. 56, 506–514 (2012).
- Puzyn, T. et al. Using nano-QSAR to predict the cytotoxicity of metal oxide nanoparticles. Nature Nanotech. 6, 175–178 (2011). · DOI
- Liu, R. et al. Development of structure–activity relationship for metal oxide nanoparticles. Nanoscale 5, 5644–5653 (2013). · DOI
- Zhang, H. et al. Use of metal oxide nanoparticle band gap to develop a predictive paradigm for oxidative stress and acute pulmonary inflammation. ACS Nano 6, 4349–4368 (2012). · DOI
- Walkey, C. D. et al. Protein corona fingerprinting predicts the cellular interaction of gold and silver nanoparticles. ACS Nano 8, 2439–2455 (2014). · DOI
- Linkov, I., Bates, M. E., Canis, L. J., Seager, T. P. & Keisler, J. A decision-directed approach for prioritizing research into the impact of nanomaterials on the environment and human health. Nature Nanotech. 6, 784–787 (2011). · DOI
- Gurevitch, J. & Hedges, L. V. in Design and Analysis of Ecological Experiments (eds Scheiner, S. M. & Gurevitch, J.) 347–371 (Oxford Univ. Press, 2001). · DOI
- Zhu, X. & Kruhlak, N. L. Construction and analysis of a human hepatotoxicity database suitable for QSAR modeling using post-market safety data. Toxicology 321, 62–72 (2014). · DOI
- Genaidy, A., Tolaymat, T., Sequeira, R., Rinder, M. & Dionysiou, D. Health effects of exposure to carbon nanofibers: systematic review, critical appraisal, meta analysis and research to practice perspectives. Sci. Total Environ. 407, 3686–3701 (2009). · DOI
- Laskowski, R. et al. Interactions between toxic chemicals and natural environmental factors—a meta-analysis and case studies. Sci. Total Environ. 408, 3763–3774 (2010). · DOI
- Gernand, J. M. & Casman, E. A. A meta-analysis of carbon nanotube pulmonary toxicity studies—how physical dimensions and impurities affect the toxicity of carbon nanotubes. Risk Anal. 34, 583–597 (2014). · DOI
- Michalet, X. et al. Quantum dots for live cells, in vivo imaging, and diagnostics. Science 307, 538–544 (2005). · DOI
- Petryayeva, E., Algar, W. R. & Medintz, I. L. Quantum dots in bioanalysis: a review of applications across various platforms for fluorescence spectroscopy and imaging. Appl. Spectr. 67, 215–252 (2013). · DOI
- Rosenthal, S. J., Chang, J. C., Kovtun, O., McBride, J. R. & Tomlinson, I. D. Biocompatible quantum dots for biological applications. Chem. Biol. 18, 10–24 (2011). · DOI
- Tsoi, K. M., Dai, Q., Alman, B. A. & Chan, W. C. W. Are quantum dots toxic? Exploring the discrepancy between cell culture and animal studies. Acc. Chem. Res. 46, 662–671 (2013). · DOI
- Winnik, F. M. & Maysinger, D. Quantum dot cytotoxicity and ways to reduce it. Acc. Chem. Res. 46, 672–680 (2013). · DOI
- Fitzpatrick, J. A. J. et al. Long-term persistence and spectral blue shifting of quantum dots in vivo. Nano Lett. 9, 2736–2741 (2009). · DOI
- Ye, L. et al. A pilot study in non-human primates shows no adverse response to intravenous injection of quantum dots. Nature Nanotech. 7, 453–458 (2012). · DOI
- Nel, A. E. et al. Understanding biophysicochemical interactions at the nano–bio interface. Nature Mater. 8, 543–557 (2009). · DOI · Paper page
- Kim, S. T., Saha, K., Kim, C. & Rotello, V. M. The role of surface functionality in determining nanoparticle cytotoxicity. Acc. Chem. Res. 46, 681–691 (2013). · DOI
- Svetnik, V. et al. Random forest: a classification and regression tool for compound classification and QSAR modeling. J. Chem. Inf. Comp. Sci. 43, 1947–1958 (2003). · DOI
- Liaw, A. & Wiener, M. Classification and regression by randomForest. R. News 2/3, 18–22 (2002).
- Braga-Neto, U. M. & Dougherty, E. R. Is cross-validation valid for small-sample microarray classification? Bioinformatics 20, 374–380 (2004). · DOI
- Efron, B. Estimating the error rate of a prediction rule—improvement on cross-validation. J. Am. Stat. Assoc. 78, 316–331 (1983). · DOI · Paper page
- Hardman, R. A toxicologic review of quantum dots: toxicity depends on physicochemical and environmental factors. Environ. Health Perspect. 114, 165–172 (2006). · DOI
- Bottrill, M. & Green, M. Some aspects of quantum dot toxicity. Chem. Commun. 47, 7039–7050 (2011). · DOI
- Yong, K. T. et al. Nanotoxicity assessment of quantum dots: from cellular to primate studies. Chem. Soc. Rev. 42, 1236–1250 (2013). · DOI
- Rzigalinski, B. A. & Strobl, J. S. Cadmium-containing nanoparticles. Perspectives on pharmacology and toxicology of quantum dots. Toxicol. Appl. Pharmacol. 238, 280–288 (2009). · DOI
- Verma, A. & Stellacci, F. Effect of surface properties on nanoparticle–cell interactions. Small 6, 12–21 (2010). · DOI
- Kroll, A. et al. Cytotoxicity screening of 23 engineered nanomaterials using a test matrix of ten cell lines and three different assays. Part. Fibre Toxicol. 8, 9 (2011). · DOI
- Bishop, C. M. Pattern Recognition and Machine Learning 2nd edn (Springer, 2007).
- Han, J. & Kamber, M. Data Mining: Concepts and Techniques 3rd edn (Elsevier, 2011).
- Nagy, A. et al. Comprehensive analysis of the effects of CdSe quantum dot size, surface charge, and functionalization on primary human lung cells. ACS Nano 6, 4748–4762 (2012). · DOI
- Chen, L. D. et al. The biocompatibility of quantum dot probes used for the targeted imaging of hepatocellular carcinoma metastasis. Biomaterials 29, 4170–4176 (2008). · DOI
- Monteiro-Riviere, N. A., Inman, A. O. & Zhang, L. W. Limitations and relative utility of screening assays to assess engineered nanoparticle toxicity in a human cell line. Toxicol. Appl. Pharmacol. 234, 222–235 (2009). · DOI · Paper page
- Kim, T. H., El-Said, W. A. & Choi, J. W. Highly sensitive electrochemical detection of potential cytotoxicity of CdSe/ZnS quantum dots using neural cell chip. Biosens. Bioelectron. 32, 266–272 (2012). · DOI
- Kumar, R., Kulkarni, A., Nagesha, D. K. & Sridhar, S. In vitro evaluation of theranostic polymeric micelles for imaging and drug delivery in cancer. Theranostics 2, 714–722 (2012). · DOI
- Chan, W. H., Shiao, N. H. & Lu, P. Z. CdSe quantum dots induce apoptosis in human neuroblastoma cells via mitochondrial-dependent pathways and inhibition of survival signals. Toxicol. Lett. 167, 191–200 (2006). · DOI
- Tang, M. et al. Unmodified CdSe quantum dots induce elevation of cytoplasmic calcium levels and impairment of functional properties of sodium channels in rat primary cultured hippocampal neurons. Environ. Health Perspect. 116, 915–922 (2008). · DOI
- Susumu, K. et al. Multifunctional compact zwitterionic ligands for preparing robust biocompatible semiconductor quantum dots and gold nanoparticles. J. Am. Chem. Soc. 133, 9480–9496 (2011). · DOI
- Kuo, T. R. et al. Studies of intracorneal distribution and cytotoxicity of quantum dots: risk assessment of eye exposure. Chem. Res. Toxicol. 24, 253–261 (2011). · DOI
- Delehanty, J. B. et al. Delivering quantum dot–peptide bioconjugates to the cellular cytosol: escaping from the endolysosomal system. Integr. Biol. 2, 265–277 (2010). · DOI
- Edmund, A. R., Kambalapally, S., Wilson, T. A. & Nicolosi, R. J. Encapsulation of cadmium selenide quantum dots using a self-assembling nanoemulsion (SANE) reduces their in vitro toxicity. Toxicol. In Vitro 25, 185–190 (2011). · DOI
- Wang, L., Nagesha, D. K., Selvarasah, S., Dokmeci, M. R. & Carrier, R. L. Toxicity of CdSe nanoparticles in Caco-2 cell cultures. J. Nanobiotechnol. 6, 11 (2008). · DOI
- Hoshino, A., Hanada, S. & Yamamoto, K. Toxicity of nanocrystal quantum dots: the relevance of surface modifications. Arch. Toxicol. 85, 707–720 (2011). · DOI
- Hoshino, A. et al. Physicochemical properties and cellular toxicity of nanocrystal quantum dots depend on their surface modification. Nano Lett. 4, 2163–2169 (2004). · DOI
- Derfus, A. M., Chan, W. C. W. & Bhatia, S. N. Probing the cytotoxicity of semiconductor quantum dots. Nano Lett. 4, 11–18 (2004). · DOI
- Smith, W. E. et al. In vitro toxicity assessment of amphiphillic polymer-coated CdSe/ZnS quantum dots in two human liver cell models. ACS Nano 6, 9475–9484 (2012). · DOI
- Zhang, H. L. et al. Special method to prepare quantum dot probes with reduced cytotoxicity and increased optical property. J. Biomed. Opt. 15, 015001 (2010). · DOI
- Chen, F. Q. & Gerion, D. Fluorescent CdSe/ZnS nanocrystal–peptide conjugates for long-term, nontoxic imaging and nuclear targeting in living cells. Nano Lett. 4, 1827–1832 (2004). · DOI
- Hoshino, A., Hanaki, K., Suzuki, K. & Yamamoto, K. Applications of T-lymphoma labeled with fluorescent quantum dots to cell tracing markers in mouse body. Biochem. Biophys. Res. Commun. 314, 46–53 (2004). · DOI
- Chang, E., Thekkek, N., Yu, W. W., Colvin, V. L. & Drezek, R. Evaluation of quantum dot cytotoxicity based on intracellular uptake. Small 2, 1412–1417 (2006). · DOI
- Zhang, T. T. et al. Cellular effect of high doses of silica-coated quantum dot profiled with high throughput gene expression analysis and high content cellomics measurements. Nano Lett. 6, 800–808 (2006). · DOI
- Liu, B. R. et al. Cellular internalization of quantum dots noncovalently conjugated with arginine-rich cell-penetrating peptides. J. Nanosci. Nanotechnol. 10, 6534–6543 (2010). · DOI
- Lee, C. M. et al. Surface engineering of quantum dots for in vivo imaging. Nanotechnology 21, 285102 (2010). · DOI
- Mahto, S. K., Park, C., Yoon, T. H. & Rhee, S. W. Assessment of cytocompatibility of surface-modified CdSe/ZnSe quantum dots for BALB/3T3 fibroblast cells. Toxicol. In Vitro 24, 1070–1077 (2010). · DOI
- Bakalova, R. et al. Chemical nature and structure of organic coating of quantum dots is crucial for their application in imaging diagnostics. Int. J. Nanomed. 6, 1719–1732 (2011). · DOI
- Zhelev, Z., Ohba, H. & Bakalova, R. Single quantum dot-micelles coated with silica shell as potentially non-cytotoxic fluorescent cell tracers. J. Am. Chem. Soc. 128, 6324–6325 (2006). · DOI
- Romoser, A. et al. Mitigation of quantum dot cytotoxicity by microencapsulation. PLoS ONE 6, e22079 (2011). · DOI
- Boeneman, K. et al. Selecting improved peptidyl motifs for cytosolic delivery of disparate protein and nanoparticle materials. ACS Nano 7, 3778–3796 (2013). · DOI
- Pathakoti, K., Hwang, H. M., Xu, H., Aguilar, Z. P. & Wang, A. In vitro cytotoxicity of CdSe/ZnS quantum dots with different surface coatings to human keratinocytes HaCaT cells. J. Environ. Sci. China 25, 163–171 (2013). · DOI
- Zhang, L. S. W., Baumer, W. & Monteiro-Riviere, N. A. Cellular uptake mechanisms and toxicity of quantum dots in dendritic cells. Nanomedicine 6, 777–791 (2011). · DOI
- Yan, M. et al. An in vitro study of vascular endothelial toxicity of CdTe quantum dots. Toxicology 282, 94–103 (2011). · DOI
- Choi, A., Cho, S. J., Desbarats, J., Lovric, J. & Maysinger, D. Quantum dot-induced cell death involves Fas upregulation and lipid peroxidation in human neuroblastoma cells. J. Nanobiotechnol. 5, 1 (2007). · DOI
- Zhou, L., Gao, C., Xu, W., Wang, X. & Xu, Y. Enhanced biocompatibility and biostability of CdTe quantum dots by facile surface-initiated dendritic polymerization. Biomacromolecules 10, 1865–1874 (2009). · DOI
- Prasad, B. R. et al. Effects of long-term exposure of gelatinated and non-gelatinated cadmium telluride quantum dots on differentiated PC12 cells. J. Nanobiotechnol. 10, 4 (2012). · DOI
- Prasad, B. R. et al. Long-term exposure of CdTe quantum dots on PC12 cellular activity and the determination of optimum non-toxic concentrations for biological use. J. Nanobiotechnol. 8, 7 (2010). · DOI
- Przybytkowski, E., Behrendt, M., Dubois, D. & Maysinger, D. Nanoparticles can induce changes in the intracellular metabolism of lipids without compromising cellular viability. FEBS J. 276, 6204–6214 (2009). · DOI
- Cho, S. J. et al. Long-term exposure to CdTe quantum dots causes functional impairments in live cells. Langmuir 23, 1974–1980 (2007). · DOI
- Li, S. et al. MicroRNAs as participants in cytotoxicity of CdTe quantum dots in NIH/3T3 cells. Biomaterials 32, 3807–3814 (2011). · DOI
- Park, S., Chibli, H., Wong, J. & Nadeau, J. L. Antimicrobial activity and cellular toxicity of nanoparticle–polymyxin B conjugates. Nanotechnology 22, 185101 (2011). · DOI
- Li, Y. et al. Chirality of glutathione surface coating affects the cytotoxicity of quantum dots. Angew. Chem. Int. Ed. 50, 5860–5864 (2011). · DOI
- Choi, A., Brown, S., Szyf, M. & Maysinger, D. Quantum dot-induced epigenetic and genotoxic changes in human breast cancer cells. J. Mol. Med. 86, 291–302 (2008). · DOI
- Lovric, J., Cho, S. J., Winnik, F. O. M. & Maysinger, D. Unmodified cadmium telluride quantum dots induce reactive oxygen species formation leading to multiple organelle damage and cell death. Chem. Biol. 12, 1227–1234 (2009). · DOI
- Su, Y. et al. The cytotoxicity of cadmium based, aqueous phase synthesized, quantum dots and its modulation by surface coating. Biomaterials 30, 19–25 (2009). · DOI
- Jan, E. et al. High-content screening as a universal tool for fingerprinting of cytotoxicity of nanoparticles. ACS Nano 2, 928–938 (2008). · DOI
- Jiang, X., Ahmed, M., Deng, Z. & Narain, R. Biotinylated glyco-functionalized quantum dots: synthesis, characterization, and cytotoxicity studies. Bioconjug. Chem. 20, 994–1001 (2009). · DOI
- Chang, S. Q. et al. UV-enhanced cytotoxicity of thiol-capped CdTe quantum dots in human pancreatic carcinoma cells. Toxicol. Lett. 188, 104–111 (2009). · DOI
- Su, Y. et al. The cytotoxicity of CdTe quantum dots and the relative contributions from released cadmium ions and nanoparticle properties. Biomaterials 31, 4829–4834 (2010). · DOI
- Steponkiene, S., Kavaliauskiene, S., Purviniene, R., Rotomskis, R. & Juzenas, P. Quantum dots affect expression of CD133 surface antigen in melanoma cells. Int. J. Nanomed. 6, 2437–2444 (2011).
- Liu, L. et al. Bioconjugated pluronic triblock-copolymer micelle-encapsulated quantum dots for targeted imaging of cancer: in vitro and in vivo studies. Theranostics 2, 705–713 (2012). · DOI
- Li, S. et al. Assessment of nanomaterial cytotoxicity with SOLiD sequencing-based microRNA expression profiling. Biomaterials 32, 9021–9230 (2011). · DOI
- Law, W. C. et al. Aqueous-phase synthesis of highly luminescent CdTe/ZnTe core/shell quantum dots optimized for targeted bioimaging. Small 5, 1302–1310 (2009). · DOI
- Liu, X. R. et al. Intracellular delivery of nanoparticles and DNAs by IR9 cell-penetrating peptides. PLoS ONE 8, e64205 (2013). · DOI
- Liu, Y. et al. The influence on cell cycle and cell division by various cadmium-containing quantum dots. Small 9, 2440–2451 (2013). · DOI
- Chang, S., Kang, B., Liu, X., Dai, Y. & Chen, D. The combined influence of surface modification, size distribution, and interaction time on the cytotoxicity of CdTe quantum dots in PANC-1 cells. Acta Biochim. Biophys. Sin. 44, 241–248 (2012). · DOI
- Corazzari, I., Gilardino, A., Dalmazzo, S., Fubini, B. & Lovisolo, D. Localization of CdSe/ZnS quantum dots in the lysosomal acidic compartment of cultured neurons and its impact on viability: potential role of ion release. Toxicol. In Vitro 27, 752–759 (2013). · DOI
- Nguyen, K. C., Willmore, W. G. & Tayabali, A. F. Cadmium telluride quantum dots cause oxidative stress leading to extrinsic and intrinsic apoptosis in hepatocellular carcinoma HepG2 cells. Toxicology 306, 114–123 (2013). · DOI
- Qu, G. B., Wang, X. Y., Wang, Z., Liu, S. J. & Jiang, G. B. Cytotoxicity of quantum dots and graphene oxide to erythroid cells and macrophages. Nanoscale Res. Lett. 8, 198 (2013). · DOI
- Wang, T. & Jiang, X. Size-dependent stability of water-solubilized CdTe quantum dots and their uptake mechanism by live HeLa cells. ACS Appl. Mater. Interfaces 5, 1190–1196 (2013). · DOI
- Xu, B., Cai, B., Liu, M. & Fan, H. Ultraviolet radiation synthesis of water dispersed CdTe/CdS/ZnS core–shell–shell quantum dots with high fluorescence strength and biocompatibility. Nanotechnology 24, 205601 (2013). · DOI
- Zheng, X. N. et al. Cytotoxicity of cadmium-containing quantum dots based on a study using a microfluidic chip. Nanotechnology 23, 055102 (2012). · DOI
- Bruneau, A. et al. In vitro immunotoxicology of quantum dots and comparison with dissolved cadmium and tellurium. Environ. Toxicol. 30, 9–25 (2013). · DOI
- Gagne, F., Maysinger, D., Andre, C. & Blaise, C. Cytotoxicity of aged cadmium-telluride quantum dots to rainbow trout hepatocytes. Nanotoxicology 2, 113–120 (2008). · DOI
- Nguyen, K. C., Seligy, V. L., & Tayabali, A. F. Cadmium telluride quantum dot nanoparticle cytotoxicity and effects on model immune responses to Pseudomonas aeruginosa. Nanotoxicology 7, 202–211 (2013). · DOI
- Tang, S., Allagadda, V., Chibli, H., Nadeau, J. L. & Mayer, G. D. Comparison of cytotoxicity and expression of metal regulatory genes in zebrafish (Danio rerio) liver cells exposed to cadmium sulfate, zinc sulfate and quantum dots. Metallomics 5, 1411–1422 (2013). · DOI
- Delehanty, J. B. et al. Self-assembled quantum dot–peptide bioconjugates for selective intracellular delivery. Bioconjug. Chem. 17, 920–927 (2006). · DOI
- Guo, G. N. et al. Probing the cytotoxicity of CdSe quantum dots with surface modification. Mater. Lett. 61, 1641–1644 (2007). · DOI
- Selvan, S. T., Tan, T. T. & Ying, J. Y. Robust, non-cytotoxic, silica-coated CdSe quantum dots with efficient photoluminescence. Adv. Mater. 17, 1620–1625 (2005). · DOI
- Tang, Y. et al. The role of surface chemistry in determining in vivo biodistribution and toxicity of CdSe/ZnS core–shell quantum dots. Biomaterials 34, 8741–8755 (2013). · DOI · Paper page
- Bae, P. K. et al. Preparation and characterization of surface-modified semiconductor quantum dot. Proc. SPIE 7270, 72701A (2013). · DOI
- Brunetti, V. et al. InP/ZnS as a safer alternative to CdSe/ZnS core/shell quantum dots: in vitro and in vivo toxicity assessment. Nanoscale 5, 307–317 (2013). · DOI
- Deka, S. et al. CdSe/CdS/ZnS double shell nanorods with high photoluminescence efficiency and their exploitation as biolabeling probes. J. Am. Chem. Soc. 131, 2948–2958 (2009). · DOI
- He, Y. et al. Microwave synthesis of water-dispersed CdTe/CdS/ZnS core–shell–shell quantum dots with excellent photostability and biocompatibility. Adv. Mater. 20, 3416–3421 (2008). · DOI
- Hu, R. et al. Functionalized near-infrared quantum dots for in vivo tumor vasculature imaging. Nanotechnology 21, 45105 (2010).
- Kim, J. S. et al. Real-time imaging of astrocyte response to quantum dots: in vivo screening model system for biocompatibility of nanoparticles. J. Colloid Interface Sci. 353, 363–371 (2011). · DOI
- Maysinger, D., Behrendt, M., Lalancette-Herbert, M. & Kriz, J. Real-time imaging of astrocyte response to quantum dots: in vivo screening model system for biocompatibility of nanoparticles. Nano Lett. 7, 2513–2520 (2007). · DOI
- Poselt, E. et al. Tailor-made quantum dot and iron oxide based contrast agents for in vitro and in vivo tumor imaging. ACS Nano 6, 3346–3355 (2012). · DOI
- Qi, L. F. & Gao, X. H. Quantum dot–amphipol nanocomplex for intracellular delivery and real-time imaging of siRNA. ACS Nano 2, 1403–1410 (2008). · DOI
- Rizvi, S. B. et al. A novel POSS-coated quantum dot for biological application. Int. J. Nanomed. 7, 3915–3927 (2012).
- Rutten, M., Janes, M. A., Laraway, B., Gregory, C. & Gregory, K. Comparison of quantum dots and CM-DiI for labeling porcine autologous bone marrow mononuclear progenitor cells. Open Stem Cell J. 2, 25–36 (2010).
- Shah, B. S., Clark, P. A., Moioli, E. K., Stroscio, M. A. & Mao, J. J. Labeling of mesenchymal stem cells by bioconjugated quantum dots. Nano Lett. 7, 3071–3079 (2007). · DOI
- Soenen, S. J., Demeester, J., De Smedt, S. C. & Braeckmans, K. The cytotoxic effects of polymer-coated quantum dots and restrictions for live cell applications. Biomaterials 33, 4882–4888 (2012). · DOI
- Tarantola, M. et al. Cytotoxicity of metal and semiconductor nanoparticles indicated by cellular micromotility. ACS Nano 3, 213–222 (2009). · DOI
- Yong, K. T., Roy, I., Law, W. C. & Hu, R. Synthesis of cRGD-peptide conjugated near-infrared CdTe/ZnSe core–shell quantum dots for in vivo cancer targeting and imaging. Chem. Commun. 46, 7136–7138 (2010). · DOI
- Yong, K. T. Mn-doped near-infrared quantum dots as multimodal targeted probes for pancreatic cancer imaging. Nanotechnology 20, 015102 (2009). · DOI
- Nagy, A. et al. Contrast of the biological activity of negatively and positively charged microwave synthesized CdSe/ZnS quantum dots. Chem. Res. Toxicol. 24, 2176–2188 (2011). · DOI
- Nagy, A. et al. Functionalization-dependent induction of cellular survival pathways by CdSe quantum dots in primary normal human bronchial epithelial cells. ACS Nano 7, 8397–8411 (2013). · DOI
- Peng, L. et al. Cellular uptake, elimination and toxicity of CdSe/ZnS quantum dots in HepG2 cells. Biomaterials 34, 9545–9558 (2013). · DOI
- Tan, S. J., Jana, N. R., Gao, S. J., Patra, P. K. & Ying, J. Y. Surface-ligand-dependent cellular interaction, subcellular localization, and vytotoxicity of polymer-coated quantum dots. Chem. Mater. 22, 2239–2247 (2010). · DOI
- Li, S. et al. Delivery of quantum dot–siRNA nanoplexes in SK-N-SH cells for BACE1 gene silencing and intracellular imaging. Mol. Ther. Nucl. Acids 1, e20 (2012). · DOI
- Adamczak, M. et al. Linseed oil based nanocapsules as delivery system for hydrophobic quantum dots. Colloids Surf. B 110, 1–7 (2013). · DOI
- Bach, L. G., Islama, M. R., Leeb, D. C. & Lim, K. T. Poly(glycidyl methacrylate) grafted CdSe quantum dots by surface-initiated atom transfer radical polymerization. Novel synthesis, characterization, properties, and cytotoxicity studies. Appl. Surf. Sci. 283, 546–553 (2013). · DOI
- Bavireddi, H. & Kikkeri, R. Glyco-beta-cyclodextrin capped quantum dots synthesis, cytotoxicity and optical detection of carbohydrate–protein interactions. Analyst 137, 5123–5127 (2012). · DOI
- Bradburne, C. E. et al. Cytotoxicity of quantum dots used for in vitro cellular labeling: role of QD surface ligand, delivery modality, cell type, and direct comparison to organic fluorophores. Bioconjug. Chem. 18, 1570–1583 (2013). · DOI
- Cao, M. Y. et al. Soft-binding ligand-capped fluorescent CdSe/ZnS quantum dots for the facile labeling of polysaccharide-based self-assemblies. Colloids Surf. B 109, 154–160 (2013). · DOI
- Ju, L. et al. Quantum dot-related genotoxicity perturbation can be attenuated by PEG encapsulation. Mut. Res. Genet. Toxicol. Environ. Mutagen. 753, 54–64 (2013). · DOI
- Liu, B. R., Liou, J. S., Huang, Y. W., Aronstam, R. S. & Lee, H. J. Determination of a threshold dose to reduce or eliminate CdTe-induced toxicity in L929 cells by controlling the exposure dose. PLoS ONE 8, e59359 (2013). · DOI
- Lv, Y., Li, K. & Li, Y. P. Surface modification of quantum dots and magnetic nanoparticles with PEG-conjugated chitosan derivatives for biological applications. Chem. Papers 67, 1404–1413 (2013). · DOI
- Qi, L. F., Shao, W. J. & Shi, D. L. JAM-2 siRNA intracellular delivery and real-time imaging by proton-sponge coated quantum dots. J. Mater. Chem. B 1, 654–660 (2013). · DOI
- Zhan, H. J. et al. One-pot aqueous-phase synthesis of ultra-small CdSe/CdS/CdZnS core–shell–shell quantum dots with high-luminescent efficiency and good stability. J. Nanopart. Res. 15, 1680 (2013). · DOI
- Zhu, Y. et al. One-pot preparation of highly fluorescent cadmium telluride/cadmium sulfide quantum dots under neutral-pH condition for biological applications. J. Colloid Interface Sci. 390, 3–10 (2013). · DOI
- Chen, N. et al. The cytotoxicity of cadmium-based quantum dots. Biomaterials 33, 1238–1244 (2012). · DOI
- Luo, Y. H. et al. Cadmium-based quantum dot induced autophagy formation for cell survival via oxidative stress. Chem. Res. Toxicol. 26, 662–673 (2013). · DOI
- Clift, M. J. D. et al. Quantum dot cytotoxicity in vitro: an investigation into the cytotoxic effects of a series of different surface chemistries and their core/shell materials. Nanotoxicology 5, 664–674 (2011). · DOI
- Clift, M. J. D. et al. The impact of different nanoparticle surface chemistry and size on uptake and toxicity in a murine macrophage cell line. Toxicol. Appl. Pharmacol. 232, 418–427 (2008). · DOI
- Cooper, D. R., Dimitrijevic, N. M. & Nadeau, J. L. Photosensitization of CdSe/ZnS QDs and reliability of assays for reactive oxygen species production. Nanoscale 2, 114–121 (2010). · DOI
- Boeneman-Gemmill, K. et al. Evaluation of diverse peptidyl motifs for cellular delivery of semiconductor quantum dots. Anal. Bioanal. Chem. 405, 6145–6154 (2013). · DOI
- Chen, L., Willoughby, A. & Zhang, J. Luminescent gelatin nanospheres by encapsulating CdSe quantum dots. Luminescence 29, 74–78 (2013). · DOI
- Zhang, Y. et al. PEOlated micelle/silica as dual-layer protection of quantum dots for stable and targeted bioimaging. Chem. Mater. 25, 2976–2985 (2013). · DOI
- Anas, A. et al. Clathrin-mediated endocytosis of quantum dot–peptide conjugates in living vells. ACS Nano 3, 2419–2429 (2009). · DOI
- Dua, P. et al. Evaluation of toxicity and gene expression changes triggered by quantum dots. Bull. Kor. Chem. Soc. 31, 1555–1560 (2010). · DOI
- Duan, H. W. & Nie, S. M. Cell-penetrating quantum dots based on multivalent and endosome-disrupting surface coatings. J. Am. Chem. Soc. 129, 3333–3338 (2007). · DOI
- Li, K. G. et al. Intracellular oxidative stress and cadmium ions release induce cytotoxicity of unmodified cadmium sulfide quantum dots. Toxicol. In Vitro 23, 1007–1013 (2009). · DOI
- Shen, L., Cui, J., Liu, J., Xu, X. & Zhu, M. The cytotoxicity of quantum dots CdSe/CdS functionalized with –COOH and –NH2 . Mater. Res. Soc. Proc. 1220, 1220–BB06–04 (2010).
- Song, E. Q. et al. Tumor cell targeting using folate-conjugated fluorescent quantum dots and receptor-mediated endocytosis. Clin. Chem. 55, 955–963 (2009). · DOI
- Stern, S. T. et al. Induction of autophagy in porcine kidney cells by quantum dots: a common cellular response to nanomaterials? Toxicol. Sci. 106, 140–152 (2008). · DOI
- Wu, C. H. et al. Probing the dynamic effect of Cys-CdTe quantum dots toward cancer cells in vitro. Chem. Res. Toxicol. 23, 82–88 (2010). · DOI
- Zhao, M. X. et al. Synthesis, biocompatibility and cell labeling of L-arginine-functional β-cyclodextrin-modified quantum dot probes. Biomaterials 31, 4401–4408 (2010). · DOI
- Seleverstov, O. et al. Quantum dots for human mesenchymal stem cells labeling. A size-dependent autophagy activation. Nano Lett. 6, 2826–2832 (2006). · DOI
- Adamczak, M. et al. Polyelectrolyte multilayer capsules with quantum dots for biomedical applications. Colloids Surf. B 90, 211–216 (2012). · DOI
- Jia, J. et al. One-step synthesis of peptide-programmed QDs as ready-to-use nanoprobes. Chem. Commun. 49, 4492–4494 (2013). · DOI
- Danner, S. et al. Quantum dots do not alter the differentiation potential of pancreatic stem cells and are distributed randomly among daughter cells. Int. J. Cell Biol. 2013, 918242 (2013). · DOI
- Song, Y., Feng, D., Shi, W., Li, X. & Ma, H. Parallel comparative studies on the toxic effects of unmodified CdTe quantum dots, gold nanoparticles, and carbon nanodots on live cells as well as green gram sprouts. Talanta 116, 237–244 (2013). · DOI
- Zhang, C. L. et al. One-pot synthesized aptamer-functionalized CdTe:Zn2+ quantum dots for tumor-targeted fluorescence imaging in vitro and in vivo. Anal. Chem. 85, 5843–5849 (2013). · DOI
- Schmidtke, C. et al. Amphiphilic, cross-linkable diblock copolymers for multifunctionalized nanoparticles as biological probes. Nanoscale 5, 7433–7444 (2013). · DOI
- Schmidtke, C. et al. Glycoconjugated amphiphilic polymers via click-chemistry for the encapsulation of quantum dots. Langmuir 29, 12593–12600 (2013). · DOI
- Bhang, S. H. et al. Hyaluronic acid–quantum dot conjugates for in vivo lymphatic vessel imaging. ACS Nano 3, 1389–1398 (2009). · DOI
- Jain, M. P., Choi, A. O., Nebibert, K. D. & Maysinger, D. Probing and preventing quantum dot-induced cytotoxicity with multimodal alpha-lipoic acid in multiple dimensions of the peripheral nervous system. Nanomedicine 4, 277–290 (2009). · DOI
- Jennings, T. L. et al. Reactive semiconductor nanocrystals for chemoselective biolabeling and multiplexed analysis. ACS Nano 5, 5579–5593 (2011). · DOI
- Kim, J. H., Park, J., Won, N., Chung, H. & Kim, S. A highly effective and facile way to prepare cellular labelling quantum dots with cetyltrimethylammonium bromide. J. Exp. Nanosci. 4, 105–112 (2009). · DOI
- Li, L. et al. Quantum dot–aluminum phthalocyanine conjugates perform photodynamic reactions to kill cancer cells via fluorescence resonance energy transfer. Nanoscale Res. Lett. 7, 386 (2012). · DOI
- Park, J. et al. Compact and stable quantum dots with positive, negative, or zwitterionic surface: specific cell interactions and non-specific adsorptions by the surface charges. Adv. Funct. Mater. 21, 1558–1566 (2011). · DOI
- Rak-Raszewska, A. et al. Quantum dots do not affect the behaviour of mouse embryonic stem cells and kidney stem cells and are suitable for short-term tracking. PLoS ONE 7, e32650 (2012). · DOI
- Rejinold, N. S., Baby, T., Nair, S. V. & Jayakumar, R. Paclitaxel loaded fibrinogen coated CdTe/ZnTe core shell nanoparticles for targeted imaging and drug delivery to breast cancer cells. J. Biomed. Nanotech. 9, 1657–1671 (2013). · DOI
- Walther, C., Meyer, K., Rennert, R. & Neundorf, I. Quantum dot–carrier peptide conjugates suitable for imaging and delivery applications. Bioconjug. Chem. 19, 2346–2356 (2008). · DOI
- Wen, C. J., Sung, C. T., Aljuffali, I. A., Huang, Y. J. & Fang, J. Y. Nanocomposite liposomes containing quantum dots and anticancer drugs for bioimaging and therapeutic delivery: a comparison of cationic, PEGylated and deformable liposomes. Nanotechnology 24, 325101 (2013). · DOI
- Wu, C. H. et al. New strategy of efficient inhibition of cancer cells by carborane carboxylic acid–CdTe nanocomposites. Nanomed. Nanotech. Biol. Med. 8, 860–869 (2012). · DOI
- Xiao, Q., Huang, S., Su, W., Chan, W. H. & Liu, Y. Facile synthesis and characterization of highly fluorescent and biocompatible N-acetyl-L-cysteine capped CdTe/CdS/ZnS core/shell/shell quantum dots in aqueous phase. Nanotechnology 23, 495717 (2012). · DOI
- Xue, B. et al. Synthesis of NAC capped near infrared-emitting CdTeS alloyed quantum dots and application for in vivo early tumor imaging. Dalton Trans. 41, 4935–4494 (2012). · DOI
- Yong, K. T., Xu, G. X. & Roy, I. Mn-doped near-infrared quantum dots as multimodal targeted probes for pancreatic cancer imaging. Chem. Commun. 47, 2901–2903 (2011). · DOI
- Zdobnova, T. A., Stremovskiy, O. A., Lebedenko, E. N. & Deyev, S. M. Self-assembling complexes of quantum dots and scFv antibodies for cancer cell targeting and imaging. PLoS ONE 7, e48248 (2012). · DOI
- Zhang, M. Z., Yu, R. N., Chen, J., Ma, Z. Y. & Zhao, Y. D. Targeted quantum dots fluorescence probes functionalized with aptamer and peptide for transferrin receptor on tumor cells. Nanotechnology 23, 485104 (2012). · DOI
- Zhao, M. X., Su, H., Mao, Z. W. & Ji, L. N. Synthesis, biocompatibility and luminescence properties of quantum dots conjugated with amino acid-functionalized beta-cyclodextrin. J. Lumin. 132, 16–22 (2012). · DOI
- Ge, C. et al. Cathodic stripping synthesis and cytotoxity studies of glutathione-capped CdTe quantum dots. J. Nanosci. Nanotech. 11, 6710–6717 (2011). · DOI
- Hsieh, M. F. et al. Tracking of cellular uptake of hydrophilic CdSe/ZnS quantum dots/hydroxyapatite composites nanoparticles in MC3T3-E1 osteoblast cells. J. Nanosci. Nanotechnol. 9, 2758–2762 (2009). · DOI
- Liu, L., Zhang, J., Su, X. & Mason, R. P. In vitro and in vivo assessment of CdTe and CdHgTe toxicity and clearance. J. Biomed. Nanotechnol. 4, 524–528 (2008). · DOI
- Wang, J. et al. Photostable water-dispersible NIR-emitting CdTe/CdS/ZnS core–shell–shell quantum dots for high-resolution tumor targeting. Biomaterials 34, 9509–9518 (2013). · DOI
- Wang, L. et al. Bioeffects of CdTe quantum dots on human umbilical vein endothelial cells. J. Nanosci. Nanotechnol. 10, 8591–8596 (2010). · DOI
- Zhang, P. et al. Click-functionalized compact quantum dots protected by multidentate-imidazole ligands: conjugation-ready nanotags for living-virus labeling and imaging. J. Am. Chem. Soc. 134, 8388–8391 (2012). · DOI
- Zheng, H., Chen, G., Song, F., DeLousie, L. A. & Lou, Z. The cytotoxicity of OPA-modified CdSe/ZnS core/shell quantum dots and its modulation by silibinin in human skin cells. J. Biomed. Nanotechnol. 7, 1–11 (2011). · DOI
- Bardi, G. et al. The biocompatibility of amino functionalized CdSe/ZnS quantum-dot-doped SiO2 nanoparticles with primary neural cells and their gene carrying performance. Biomaterials 31, 6555–6566 (2010). · DOI
- Cai, W. J. et al. High quality CdHgTe nanocrystals with strong near-infrared emission: relationship between composition and cytotoxic effects. Langmuir 29, 4119–4127 (2013). · DOI
- Chahal, D. S., Chahal, H. S., Bayles, A. R., Rudie, E. M. & Helms, B. A. Synthetic development of cell-permeable polymer colloids decorated with nanocrystal imaging probes optimized for cell tracking. Chem. Sci. 3, 2246–2251 (2012). · DOI
- Chakraborty, S., Gogoi, M., Kalita, E. & Deb, P. Multifunctional, high luminescent, biocompatible CdTe quantum dot fluorophores for bioimaging applications. Int. J. Nanosci. 10, 1191–1195 (2011). · DOI
- Generalov, R., Lukoseviciute, S., Juzeniene, A. & Juzenas, P. Cytotoxicity and phototoxicity of red fluorescent nontargeted quantum dots. IEEE J. Sel. Top. Quantum Electron. 16, 997–1003 (2010). · DOI
- GhoshMitra, S., Diercks, D. R., Mills, N. C., Hynds, D. L. & Ghosh, S. Excellent biocompatibility of semiconductor quantum dots encased in multifunctional poly(N-isopropylacrylamide) nanoreservoirs and nuclear specific labeling of growing neurons. Appl. Phys. Lett. 98, 103702 (2011). · DOI
- Goo, S., Choi, Y. J., Lee, Y., Lee, S. & Chung, H. W. Selective effects of curcumin on CdSe/ZnS quantum-dot-induced phototoxicity using UVA irradiation in normal human lymphocytes and leukemia cells. Toxicol. Res. 29, 35–42 (2013). · DOI
- Han, S. & Li, Q. Cytotoxicity effects of CdTe quantum dots on human lung cancer A549 cells. Key Eng. Mater. 531, 504–507 (2013).
- Hu, D. H. et al. A fast synthesis of near-infrared emitting CdTe/CdSe quantum dots with small hydrodynamic diameter for in vivo imaging probes. Nanoscale 3, 4724–4732 (2011). · DOI
- Kim, B. Y. S. et al. Biodegradable quantum dot nanocomposites enable live cell labeling and imaging of cytoplasmic targets. Nano Lett. 8, 3887–3892 (2008). · DOI
- Lee, S. J. et al. Sonication treatment of CdTe/CdS semiconductor nanocrystals and their bio-application. Chem. Commun. 2008, 5574–5576 (2008). · DOI
- Li, J. M. et al. Multifunctional quantum-dot-based siRNA delivery for HPV18 E6 gene silence and intracellular imaging. Biomaterials 32, 7978–7987 (2011). · DOI
- Li, X. et al. Autophagy-sensitized cytotoxicity of quantum dots in PC12 cells. Adv. Healthcare Mater. 3, 354–359 (2013). · DOI
200 of 342 shown
Cited by
Sorted by citations
Machine learning in materials science
Wei, J., Chu, X., Sun, X., Xu, K., Deng, H., Chen, J., Wei, Z., & Lei, M. (2019) · InfoMat · doi:10.1002/inf2.12028 · Cited by 1,069
Muratov, E. N., Bajorath, J., Sheridan, R. P., Tetko, I. V., Filimonov, D., Poroikov, V., Oprea, T. I., Baskin, I. I., Varnek, A., Roitberg, A., et al. (2020) · Chemical Society Reviews · doi:10.1039/d0cs00098a · Cited by 913
Self-citationDependence of Nanoparticle Toxicity on Their Physical and Chemical Properties
Sukhanova, A. V., Bozrova, S. V., Sokolov, P. M., Berestovoy, M. A., Karaulov, A. V., & Nabiev, I. R. (2018) · Nanoscale Research Letters · doi:10.1186/s11671-018-2457-x · Cited by 1,170
“It has been shown that the QD nanotoxicity is closely correlated with their surface properties (including shell, ligand, and surface modifications), diameter, toxicity assay type used, and the exposure time [58].”
BackgroundHildebrandt, N., Spillmann, C. M., Algar, W. R., Pons, T., Stewart, M. H., Oh, E., Susumu, K., Díaz, S. A., Delehanty, J. B., & Medintz, I. L. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00030 · Cited by 748
Self-citationManickam, P., Mariappan, S. A., Murugesan, S. M., Hansda, S., Kaushik, A. K., Shinde, R. B., & Thipperudraswamy, S. P. (2022) · Biosensors · doi:10.3390/bios12080562 · Cited by 717
“AI aided immunohistochemical method to detect the multi-tumor, which overcomes the sensitivity limitation of the manual immunohistochemical method.”
Method
Metadata
- Authors
- Oh, E., Liu, R., Nel, A., Gemill, K. B., Bilal, M., Cohen, Y., & Medintz, I. L.
- Affiliations
- United States Naval Research Laboratory (US)
- University of California, Los Angeles (US)
- Corresponding author
- Liu, Rong
- Cohen, Yoram
- Medintz, Igor L.
- Venue
- Nature Nanotechnology
- Published
- 2016-02-29
- Volume
- 11
- Issue
- 5
- Pages
- 479-486
- ISSN
- 1748-3387 (ISSN-L)
- 1748-3395
- OpenAlex
- W2292437912
- Cited by
- 502
- References
- 0
- Citations by year
- 2026: 24 · 2025: 36 · 2024: 39 · 2023: 40 · 2022: 62 · 2021: 53 · 2020: 78 · 2019: 44 · 2018: 56 · 2017: 48 · 2016: 22
- FWCI
- 2.26
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Nanotechnology (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Science Foundation
- Defense Threat Reduction Agency
- U.S. Naval Research Laboratory
- Topics
- Physical Sciences › Materials Science › Materials Chemistry › Quantum Dots Synthesis And Properties
- Physical Sciences › Materials Science › Materials Chemistry › Nanoparticles: synthesis and applications
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Heavy Metal Exposure and Toxicity
- Keywords
- cadmium quantum dots, semiconductor quantum dots, cytotoxicity, engineered nanomaterials, nanoparticle toxicity, cell viability, surface modification, ligands, shells, particle diameter, toxicity prediction, physicochemical properties, random forest regression
- MeSH terms
- Animals, Cadmium, Cell Survival, Humans, Models, Theoretical, Inhibitory Concentration 50, Quantum Dots, Workflow
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review