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Detection of irradiated quail meat by using DNA comet assay and evaluation of comets by image analysis

机译:利用DNA彗星试验检测辐照鹌鹑肉并通过图像分析评价彗星。

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A simple technique of microgel electrophoresis of single cells (DNA comet assay) was used to detect DNA comets in irradiated quail meat samples. Obtained DNA comets were evaluated by both photomicrographic and image analysis. Quail meat samples were exposed to radiation doses of 0.52, 1.05,1.45, 2.00, 2.92 and 4.00 kGy in gamma cell (gammacell ~(60)Co, dose rate 1.31 kGy/h) covering the permissible limits for enzymatic decay and stored at 2 °C. The cells isolated from muscle (chest, thorax) in cold PBS were analyzed using the DNA comet assay on 1, 2, 3, 4, 7, 8 and 11 day post irradiation. The cells were lysed between 2,5 and 9 min in 2.5% SDS and electrophoresis was carried out at a voltage of 2V/cm for 2 min. After propidium iodide staining, the slides were evaluated through a fluorescent microscope. In all irradiated samples, fragmented DNA stretched towards the anode and damaged cells appeared as a comet. All measurement data were analyzed using BS 200 ProP with software image analysis (BS 200 ProP, BAB Imaging System, Ankara, Turkey). The density of DNA in the tails increased with increasing radiation dose. However, in non-irradiated samples, the large molecules of DNA remained relatively intact and there was only minor or no migration of DNA; the cells were round or had very short tails only. The values of tail DNA%, tail length and tail moment were significantly different and identical between 0.9 and 4.0 kGy dose exposure, and also among storage times on day 1,4 and 8. In conclusion, the DNA Comet Assay EN 13784 standard method may be used not only for screening method for detection of irradiated quail meat depending on storage time and condition but also for the quantification of applied dose if it is combined with image analysis. Image analysis may provide a powerful tool for the evaluation of head and tail of comet intensity related with applied doses.
机译:一种简单的单细胞微凝胶电泳技术(DNA彗星试验)被用于检测辐照鹌鹑肉样品中的DNA彗星。通过显微照相和图像分析来评估获得的DNA彗星。鹌鹑肉样品在γ细胞中(伽马细胞〜(60)Co,剂量率1.31 kGy / h)暴露于0.52、1.05、1.45、2.00、2.92和4.00 kGy的辐射剂量下,其酶促降解极限,并保存在2 ℃。在照射后1、2、3、4、7、8和11天,使用DNA彗星分析法分析冷PBS中从肌肉(胸部,胸部)分离出的细胞。在2.5%SDS中在2.5至9分钟之间裂解细胞,并以2V / cm 2的电压进行电泳2分钟。碘化丙啶染色后,通过荧光显微镜评估载玻片。在所有辐照的样品中,碎片化的DNA向阳极延伸,受损的细胞像彗星一样出现。使用带有软件图像分析的BS 200 ProP(BS 200 ProP,BAB Imaging System,土耳其安卡拉)分析所有测量数据。尾巴中的DNA密度随着辐射剂量的增加而增加。但是,在未经辐照的样品中,大分子DNA保持相对完整,并且只有少量或没有DNA迁移。细胞圆形或只有短尾巴。在0.9和4.0 kGy剂量暴露之间以及在第1,4和8天的储存时间之间,尾巴DNA%,尾巴长度和尾矩的值显着不同且相同。总而言之,DNA彗星试验EN 13784标准方法可能不仅可以用于根据存储时间和条件检测辐照鹌鹑肉的筛选方法,而且还可以与图像分析相结合来量化所施加的剂量。图像分析可以为评估与剂量相关的彗星强度的头和尾提供强大的工具。

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