2012
DOI: 10.1007/s11051-012-1137-5
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Cytotoxicity evaluation of nanoclays in human epithelial cell line A549 using high content screening and real-time impedance analysis

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Cited by 70 publications
(49 citation statements)
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“…Some (Byrne and Baugh 2008, Nel et al 2006) have expressed concern that nanoparticles can be dangerous and that platelet and tubular Al nanoclays are cytotoxic (e.g., Lordan and Higginbotham 2012, Lordan et al 2011, Verma et al 2012, Wallace et al 1985). However there is little correlation between Al nanoparticle toxicity in vitro and that observed in vivo, partly because the physical properties of the primary Al nanoparticles differ from the larger aggregates (Al nanoclusters) (Murdock et al 2008) to which people are exposed.…”
Section: Synthesis and Conclusionmentioning
confidence: 99%
“…Some (Byrne and Baugh 2008, Nel et al 2006) have expressed concern that nanoparticles can be dangerous and that platelet and tubular Al nanoclays are cytotoxic (e.g., Lordan and Higginbotham 2012, Lordan et al 2011, Verma et al 2012, Wallace et al 1985). However there is little correlation between Al nanoparticle toxicity in vitro and that observed in vivo, partly because the physical properties of the primary Al nanoparticles differ from the larger aggregates (Al nanoclusters) (Murdock et al 2008) to which people are exposed.…”
Section: Synthesis and Conclusionmentioning
confidence: 99%
“…Verma et al (2012) compared the toxicity of both structures in the lung epithelial cells A549 and showed that the platelet-structured nanoclays were more cytotoxic than the tubular types. It is important to note that the structure was not the only difference among them because the nature of the clay mineral also differed.…”
Section: Basal Cytotoxicity Assays and Morphological Studiesmentioning
confidence: 99%
“…Previous studies have shown that mammalian cell cytotoxicity of PEIs depend upon the polymer molecular weight and exposure time [35]. To obtain a better insight into possible LPEI/BPEI-induced mammalian toxicity, we used High Content Analysis (HCA), a high throughput quantitative data acquisition method for determining changes in cellular behaviour and morphotypes [60][61][62]. For this study, human dermal fibroblasts (hDFs) cells were exposed to various concentrations of the polymers for 24 h, fluorescently stained with nuclear and cytoplasmic markers and analysed by using an automated INCell Analyzer 2200.…”
Section: In Vitro Evaluation Of Membrane Selectivity Of Lpei and Bpeimentioning
confidence: 99%