啁啾激发产生的空间编码纯漂移扩散有序核磁共振光谱学

IF 2 3区 化学 Q3 BIOCHEMICAL RESEARCH METHODS
Rituraj Mishra , Jonathan R.J. Yong , Corentin Jacquemmoz , Benjamin Lorandel , Mohammadali Foroozandeh , Jean-Nicolas Dumez
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引用次数: 0

摘要

空间编码扩散有序核磁共振波谱(SPEN-DOSY)是分析溶液中小分子混合物的一种新的省时工具。时间效率是通过有效梯度区域的空间并行化概念来实现的,而不是传统扩散实验中使用的顺序递增。使用这种序列获取的数据通常经过处理后可提取扩散系数,但 1H 光谱中出现峰值重叠的情况很难处理。传统扩散实验中的这种限制可通过使用啁啾激发产生的纯移位(PSYCHE)-iDOSY 序列来解决。在这里,我们利用回波平面光谱成像(EPSI)对 PSYCHE-iDOSY 序列进行了调整,以获取 SPEN-DOSY 数据。PSYCHE 的纯移位模式可分离重叠成分,并利用修改后的 Stejskal-Tanner 方程提取相应的扩散系数。利用上述混合物获得的主要结果似乎为在比 PSYCHE-iDOSY 更短的时间内分离复杂混合物提供了可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spatially encoded pure-shift diffusion-ordered NMR spectroscopy yielded by chirp excitation

Spatially encoded pure-shift diffusion-ordered NMR spectroscopy yielded by chirp excitation

Spatially-encoded diffusion-ordered NMR spectroscopy (SPEN-DOSY) has emerged as a new time-efficient tool for the analysis of mixtures of small molecules in solution. Time efficiency is achieved using the concept of spatial parallelization of the effective gradient area, instead of the sequential incrementation used in conventional diffusion experiments. The data acquired with such sequences are then usually processed to extract diffusion coefficients, but cases when peak overlap in the 1H spectrum are difficult to address. Such limitation in conventional diffusion experiments is addressed via using the Pure Shift Yielded by CHirp Excitation (PSYCHE)-iDOSY sequence. Here we have adapted the PSYCHE-iDOSY sequence by using echo planar spectroscopic imaging (EPSI) to acquire SPEN-DOSY data. The pure shift mode of PSYCHE separates the overlapped components and a modified Stejskal-Tanner equation is used to extract the corresponding diffusion coefficient. The primary results obtained with the above-mentioned mixtures seem to open the possibility of separating complex mixtures in less time than PSYCHE-iDOSY.

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来源期刊
CiteScore
3.80
自引率
13.60%
发文量
150
审稿时长
69 days
期刊介绍: The Journal of Magnetic Resonance presents original technical and scientific papers in all aspects of magnetic resonance, including nuclear magnetic resonance spectroscopy (NMR) of solids and liquids, electron spin/paramagnetic resonance (EPR), in vivo magnetic resonance imaging (MRI) and spectroscopy (MRS), nuclear quadrupole resonance (NQR) and magnetic resonance phenomena at nearly zero fields or in combination with optics. The Journal''s main aims include deepening the physical principles underlying all these spectroscopies, publishing significant theoretical and experimental results leading to spectral and spatial progress in these areas, and opening new MR-based applications in chemistry, biology and medicine. The Journal also seeks descriptions of novel apparatuses, new experimental protocols, and new procedures of data analysis and interpretation - including computational and quantum-mechanical methods - capable of advancing MR spectroscopy and imaging.
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