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Comparison of C_(60) and GCIB primary ion beams for the analysis of cancer cells and tumour sections (Conference Paper)

机译:C_(60)和GCIB一次离子束在分析癌细胞和肿瘤切片中的比较(会议论文)

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摘要

We have implemented a gas cluster ion beam (GCIB) system developed by Ionoptika Ltd (Southampton, UK) with sufficient control to allow us to exploit the unique capabilities of our J105 instrument for imaging and depth profiling. The J105 allows us to use the GCIB as continuous primary ion beam, thereby overcoming the issues associated with pulsing these slow moving, mixed species beams. We have performed a direct comparison with C_(60) ions on the same samples in the same instrument. The GCIB beams are more difficult to focus than the C_(60) ~+ ion beam, making single-cell imaging difficult, although spot sizes of 15-20 μm are readily obtainable for Ar _(1000) and Ar_(2000), providing good resolution for larger area imaging on tissue section/biopsy samples. In this paper, we present results from the assessment of these new beams as primary ions for the analysis of 'real', complex biological systems. Initial spectra and those following increased primary ion bombardment were compared for in vitro cultured cells deposited on silicon and cryo-sectioned tumour samples originating in vivo. Ar_(1000) ~+ and Ar_(2000) ~+ showed increased persistence of the signals from intact molecular ions of phospholipids and a reduction in the accumulation of chemical background noise compared with C _(60) ~+ analysis.
机译:我们已经实施了由Ionoptika Ltd(英国南安普敦)开发的气体团簇离子束(GCIB)系统,该系统具有足够的控制能力,使我们能够利用J105仪器的独特功能进行成像和深度剖析。 J105允许我们将GCIB用作连续的主离子束,从而克服了与脉冲这些缓慢移动的混合物种束相关的问题。我们对同一仪器中相同样品上的C_(60)离子进行了直接比较。 GCIB束比C_(60)〜+离子束更难聚焦,从而使单细胞成像变得困难,尽管Ar_(1000)和Ar_(2000)的光斑尺寸很容易获得15-20μm。对组织切片/活检样本进行大面积成像的高分辨率。在本文中,我们将这些新束的评估结果作为主要离子,用于分析“真实”的复杂生物系统。对沉积在硅上的体外培养细胞和体内起源的冰冻切片肿瘤样品的初始光谱和增加的一次离子轰击后的光谱进行了比较。与C _(60)〜+分析相比,Ar_(1000)〜+和Ar_(2000)〜+显示了来自完整分子磷脂的信号的持久性增加,化学背景噪声的累积减少。

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