首页> 外文会议>Conference on Novel Optical Instrumentation for Biomedical Applications; Jun 24-25, 2003; Munich, Germany >A Cross-Correlated Experimental Set-Up For Probing Normal And Abnormal Vital Processes That Are Endogenous Or Induced By Xenobiotic Agents
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A Cross-Correlated Experimental Set-Up For Probing Normal And Abnormal Vital Processes That Are Endogenous Or Induced By Xenobiotic Agents

机译:一种相互关联的实验装置,用于探测由异源生物制剂引起的正常和异常的生命过程

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A wealth of data point to Delayed Luminescence (DL) as a good candidate for early and reliable detection technique in neoplastic cells and tissues sorting. Aiming at a DL experimental set up for such a kind of information, a testing technique for morphological analysis should be provided. This could certify the early identification of pathologies and abnormalities in, cells and tissues by DL. DL technique may be coupled with FIB (Focused Ion Beam) imaging analysis to give a correlated, both spectroscopic and morphological investigation, at the submicron scale. A strong link among others has been reported to exist between DL signal characteristics and cytoskeleton structure and dynamics: FIB (Focused Ion Beam) imaging is for the moment being the best non invasive check at all and it can detect morphological alterations as early as possible since its resolution can go down to 2-5 nm. The cells, that can be highlighted by the fast DL and slow and efficient FIB. can be in parallel analysed by a metabolic manometric technique that uses differential pressure sensors: the different cellular activity of normal and abnormal cells can be recorded and this allows fast and non-invasive investigations, although requiring a minimal number of cells. In addition it's possible to study, by the confocal microscopy spectroscopic analysis, DNA fragments, exploiting the optical characteristics of a dye, like ethidium bromide, to detect dynamic and conformational changes in DNA chains. These changes can be artificially induced in cells (e.g. by irradiation) or found in neoplastic cells. The acquired experience allows an independent check of spectroscopic, morphologic and metabolic testing by a control on nucleic acid defects. These four techniques may be used together creating a "protocol" in order to permit an early and reliable alterations diagnosis of cells and tissues, guaranteeing an high accuracy standard.
机译:大量数据表明,延迟发光(DL)是肿瘤细胞和组织分类中早期可靠的检测技术的良好选择。针对针对此类信息的DL实验设置,应提供一种用于形态分析的测试技术。这可以证明通过DL可以早期识别细胞和组织中的病理和异常。 DL技术可以与FIB(聚焦离子束)成像分析结合使用,以提供亚微米级的相关光谱学和形态学研究。据报道,DL信号特征与细胞骨架结构和动力学之间存在着很强的联系:FIB(聚焦离子束)成像目前是最好的非侵入性检查,它可以尽早发现形态改变。它的分辨率可以降至2-5 nm。可以通过快速DL和缓慢而有效的FIB突出显示这些单元。可以通过使用压差传感器的代谢测压技术进行并行分析:可以记录正常细胞和异常细胞的不同细胞活动,尽管需要的细胞数量最少,但可以进行快速且无创的研究。此外,还可以通过共聚焦显微镜分析法研究DNA片段,从而利用染料(如溴化乙锭)的光学特性来检测DNA链中的动态和构象变化。这些变化可以在细胞中人工诱导(例如通过辐射)或在赘生性细胞中发现。获得的经验可以通过控制核酸缺陷来独立检查光谱,形态和代谢测试。可以将这四种技术一起使用以创建“协议”,以便对细胞和组织进行早期而可靠的变更诊断,从而确保了高精度标准。

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