2005
DOI: 10.1016/j.mrgentox.2004.10.003
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Using fluorescence for improvement of the quantitative analysis of micronucleus in cell culture

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Cited by 21 publications
(15 citation statements)
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“…Interphase cytogenetics is especially useful in genotoxicity studies as most mutagens decrease mitotic activity. Recently, the MN test with fluorescent stains proved to be more sensitive in detecting small micronuclei compared to the MN test using traditional methods, such as Feulgen’s reaction (Dias et al 2005). Therefore, the use of fluorescence has been proposed as an accurate method for the detection of micronuclei.…”
Section: Introductionmentioning
confidence: 99%
“…Interphase cytogenetics is especially useful in genotoxicity studies as most mutagens decrease mitotic activity. Recently, the MN test with fluorescent stains proved to be more sensitive in detecting small micronuclei compared to the MN test using traditional methods, such as Feulgen’s reaction (Dias et al 2005). Therefore, the use of fluorescence has been proposed as an accurate method for the detection of micronuclei.…”
Section: Introductionmentioning
confidence: 99%
“…Other studies also point to the role of nanoparticles in mediated DNA damages owing to the development of oxidative stress [15][16][17]. To estimate changes in the stability of cell genomes in systems in vivo and in vitro through the action of nano composites and nanoparticles, various methodological approaches are used, one of which is the MN test [5,10,11,18]. Modern researchers offer different ways of FM action, depending on their size and stabi lizer.…”
Section: Resultsmentioning
confidence: 99%
“…The number of micronuclei (MN) was evaluated on preparations col ored with acridine orange (3.0 mg/mL in a phosphate buffer with pH 6.4-6.5) for 1000 AEC cells with the help of a Micros MS 300 fluorescent microscope (40 × 10) [11].…”
Section: Methodsmentioning
confidence: 99%
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“…The mean frequency of MNIE in concurrent positive controls is higher in the first experiment (69.5 ± 11.7 MNIE/1000 IEs) compared to the second one (46.5 ± 7.7 MNIE/1000 IEs), evidencing the difference between the two different scoring methods applied in the main experiment and in the second one. The use of propidium iodide, counterstain for the DNA in the second experiment, presents advantages compared to acridine orange: the fluorescence is long lasting and longer than AO (Dias et al, 2005) • Individual data for MNIE/1000 cells (24.0, 33.5, 6.5, 8.0, 29.0) for buprofezin 2000 mg/kg in the first experiment, reveal a large interindividual variability.…”
mentioning
confidence: 99%