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Uncovering New Challenges In Bio-analysis With Tof-sims

机译:用Tof-sims发现生物分析中的新挑战

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The introduction of cluster ion beams for routine SIMS analysis has greatly improved the prospects for characterising biological samples. The ultimate quality of the secondary ion image remains limited by the efficiency of the primary beam. Without overcoming the low ionisation probabilities associated with SIMS, the highest lateral resolution available for molecular imaging becomes limited by the statistical probability of any ions being generated from the area of the pixel. C_(60)~+ primary ions are currently the most efficient available for routine analysis but although commercial systems have been demonstrated to produce spot sizes under 200 nm, focusing the beam produced in such electron impact sources results in rather low ion currents. The time scale for such high lateral resolution analysis can become impractical on conventional time-of-flight instruments. Molecular depth profiling capability has been revealed using SF_5~+ and C_(60)~+ ion beams and recent work has advanced the technique by combining the profiling and imaging abilities of these high efficiency projectiles to generate 3D molecular maps of biological systems. In this paper we discuss the challenges associated with 2D and 3D bio-analysis with emphasis on how instrumental advances aid such investigations yet demonstrating the obstacles that need to be overcome using a range of model and real world biological samples. We discuss complications with the biological matrix, challenges in manipulating and visualising the data and look at how instrumental advantages might aid the routine generation of these 3D molecular maps.
机译:用于常规SIMS分析的簇离子束的引入极大地改善了表征生物样品的前景。次级离子图像的最终质量仍然受到初级束效率的限制。在不克服与SIMS相关的低电离概率的情况下,可用于分子成像的最高横向分辨率受到从像素区域生成任何离子的统计概率的限制。 C_(60)〜+初级离子是目前用于常规分析的最有效的离子,但是尽管已证明商用系统可产生200 nm以下的光斑,但聚焦在此类电子撞击源中产生的电子束会产生相当低的离子电流。这种高横向分辨率分析的时间标度在常规飞行时间仪器上变得不切实际。利用SF_5〜+和C_(60)〜+离子束已经揭示了分子深度轮廓分析功能,并且最近的工作通过结合这些高效弹丸的轮廓分析和成像功能来生成生物系统的3D分子图谱,从而提高了该技术。在本文中,我们将讨论与2D和3D生物分析相关的挑战,重点是仪器的改进如何帮助此类研究,同时说明使用一系列模型和现实世界的生物样本需要克服的障碍。我们讨论了生物基质的并发症,在处理和可视化数据方面的挑战,并探讨了仪器的优势如何有助于常规生成这些3D分子图。

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