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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >Fast and facile preparation of nanostructured silicon surfaces for laser desorption/ionization mass spectrometry of small compounds
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Fast and facile preparation of nanostructured silicon surfaces for laser desorption/ionization mass spectrometry of small compounds

机译:用于小化合物的激光解吸/电离质谱的纳米结构硅表面的快速和容易制备

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Rationale Many important biological processes rely on specific biomarkers (such as metabolites, drugs, proteins or peptides, carbohydrates, lipids, ...) that need to be monitored in various fluids (blood, plasma, urine, cell cultures, tissue homogenates, horizontal ellipsis ). Although mass spectrometry (MS) hyphenated to liquid chromatography (LC) is widely accepted as a 'gold-standard' method for identifying such synthetic chemicals or biological products, their robust fast sensitive detection from complex matrices still constitutes a highly challenging matter. Methods In order to circumvent the constraints intrinsic to LC/MS technology in terms of prior sample treatment, analysis time and overall method development to optimize ionization efficiency affecting the detection threshold, we investigated laser desorption/ionization mass spectrometry (LDI-MS) by directly depositing the sample under study onto cheap inert nanostructures made of silicon to perform straightforward sensitive and rapid screening of targeted low mass biomarkers on a conventional MALDI platform. Results The investigated silicon nanostructures were found to act as very efficient ion-promoting surfaces exhibiting high performance for the detection of different classes of organic compounds, including glutathione, glucose, peptides and antibiotics. Achieving such broad detection was compulsory to develop a SALDI-MS-based pre-screening tool. Conclusions The key contribution of the described analytical strategy consists of designing inert surfaces that are fast (minute preparation) and cheap to produce, easy to handle and able to detect small organic compounds in matrix-free LDI-MS prerequisite for biomarkers pre-screening from body fluids without the recourse of any separation step.
机译:理由许多重要的生物过程依赖于特定的生物标志物(例如代谢物,药物,蛋白质或肽,碳水化合物,脂质,......),需要在各种流体(血液,血浆,尿液,细胞培养物,组织匀浆,水平省略号)。虽然将质谱(MS)连字体与液相色谱(LC)被广泛接受为鉴定这种合成化学品或生物产品的“金标准”方法,但它们从复杂基质的稳健敏感检测仍然构成了一个非常具有挑战性的物质。方法为了在先前的样品处理,分析时间和总体方法开发方面规避限制的限制,以优化影响检测阈值的电离效率,直接研究了激光解吸/电离质谱(LDI-MS)的电离效率将样品置于研究中,进入由硅制成的廉价惰性纳米结构,在传统的MALDI平台上对靶向低质量生物标志物进行直接敏感和快速筛选。结果发现研究的硅纳米结构作为非常有效的离子促进表面,其表现出对不同类别的有机化合物的高性能,包括谷胱甘肽,葡萄糖,肽和抗生素。实现这种广泛的检测是强制性的,以开发基于SALDI-MS的预筛选工具。结论所述分析策略的主要贡献包括设计惰性表面,这些惰性表面快速(分钟制备)和廉价生产,易于处理,并且能够检测到无基质LDI-MS中的小有机化合物,用于预筛选生物标志物的生物标志物体液没有追索任何分离步骤。

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    Univ Valenciennes IEMN UMR CNRS 8520 Univ Lille CNRS Cent Lille ISEN Ave Poincare BP 60069 F-59652 Villeneuve Dascq France;

    Univ Montpellier Inst Biomol Max Mousseron Pl Eugene Bataillon F-34095 Montpellier France;

    Inst Biol Lille UMR CNRS 8160 F-59000 Lille France;

    Univ Valenciennes IEMN UMR CNRS 8520 Univ Lille CNRS Cent Lille ISEN Ave Poincare BP 60069 F-59652 Villeneuve Dascq France;

    Inst Biol Lille UMR CNRS 8160 F-59000 Lille France;

    Res &

    Technol Ctr Energy Lab Semicond Nano Struct &

    Adv Technol Borj Cedria Sci &

    Technol Pk BP 95 Hammam Lif 2050 Tunisia;

    Univ Valenciennes IEMN UMR CNRS 8520 Univ Lille CNRS Cent Lille ISEN Ave Poincare BP 60069 F-59652 Villeneuve Dascq France;

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  • 正文语种 eng
  • 中图分类 分析化学;
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