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Sample-First Preparation: A Method for Surface-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry Analysis of Cyclic Oligosaccharides

机译:样品优先制备:环状寡糖的表面辅助激光解吸/电离飞行时间质谱分析方法

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摘要

A new sample preparation method for the analysis of cyclicoligosaccharides in surface-assisted laser desorption/ionization mass spectrometry (SALDI-MS) is presented. We call this new technique "sample first method", in which a sample is deposited first and then bare gold nanoparticles (AuNPs), which serve as the SALDI matrixes, are added to the top of the sample layer. The use of the sample first method offers significant advantages for improving shot-to-shot reproducibility, enhancing the ionization efficiency of the analyte, and reducing sample preparation time as compared to the dried-droplet method, wherein samples and bare AuNPs are mixed and dried together. The relative standard deviation (RSD) values of the signal intensity as calculated from 65 sample spots was 25percent when the sample first methods were applied to the analysis of beta-cyclodextrin. The results were more homogeneous as compared to the outcome using dried-droplet preparation of AuNPs (RSD velence 66percent) and 2,5-dihydroxybenzoic acid (RSD velence 209percent). We also found out that the optimal concentration of AuNP for ionization efficiency is 7.4 nM (4.52 X 10~(12) particles/mL) while the lowest detectable concentration of cyclic oligosaccharides through this approach is 0.25 (mu)M. Except for the cyclic oligosaccharide, the proposed method was also applied to the analyses of other biological samples, including neutral carbohydrate and steroid, aminothiols, and peptides as well as proteins.
机译:提出了一种在表面辅助激光解吸/电离质谱(SALDI-MS)中分析环寡糖的新样品前处理方法。我们称这种新技术为“样品优先方法”,其中先沉积样品,然后将用作SALDI基质的裸金纳米颗粒(AuNPs)添加到样品层的顶部。与将样品和裸金纳米粒子混合并干燥的干滴法相比,使用样品优先方法具有显着的优势,可提高逐次重现性,增强分析物的电离效率并减少样品制备时间。一起。当采用样品优先方法对β-环糊精进行分析时,由65个样品斑点计算出的信号强度的相对标准偏差(RSD)值为25%。与使用干液滴制备AuNPs(RSD velence 66%)和2,5-二羟基苯甲酸(RSD velence 209%)的结果相比,结果更加均匀。我们还发现,用于电离效率的AuNP的最佳浓度为7.4 nM(4.52 X 10〜(12)颗粒/ mL),而通过这种方法可检测到的最低的环状寡糖浓度为0.25μM。除环状寡糖外,该方法还适用于其他生物样品的分析,包括中性碳水化合物和类固醇,氨基硫醇,肽以及蛋白质。

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