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采用液滴涂层沉积法对血浆和血清进行振动光谱研究及其在临床中的应用。

Vibrational Spectroscopic Investigation of Blood Plasma and Serum by Drop Coating Deposition for Clinical Application.

机构信息

Institute of Physical Chemistry and Abbe Center of Photonics, Friedrich-Schiller-University, Helmholtzweg 4, D-07743 Jena, Germany.

Leibniz Institute of Photonic Technology, Member of Leibniz Health Technologies, Albert-Einstein-Straße 9, D-07745 Jena, Germany.

出版信息

Int J Mol Sci. 2021 Feb 22;22(4):2191. doi: 10.3390/ijms22042191.

DOI:10.3390/ijms22042191
PMID:33671841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7926873/
Abstract

In recent decades, vibrational spectroscopic methods such as Raman and FT-IR spectroscopy are widely applied to investigate plasma and serum samples. These methods are combined with drop coating deposition techniques to pre-concentrate the biomolecules in the dried droplet to improve the detected vibrational signal. However, most often encountered challenge is the inhomogeneous redistribution of biomolecules due to the coffee-ring effect. In this study, the variation in biomolecule distribution within the dried-sample droplet has been investigated using Raman and FT-IR spectroscopy and fluorescence lifetime imaging method. The plasma-sample from healthy donors were investigated to show the spectral differences between the inner and outer-ring region of the dried-sample droplet. Further, the preferred location of deposition of the most abundant protein albumin in the blood during the drying process of the plasma has been illustrated by using deuterated albumin. Subsequently, two patients with different cardiac-related diseases were investigated exemplarily to illustrate the variation in the pattern of plasma and serum biomolecule distribution during the drying process and its impact on patient-stratification. The study shows that a uniform sampling position of the droplet, both at the inner and the outer ring, is necessary for thorough clinical characterization of the patient's plasma and serum sample using vibrational spectroscopy.

摘要

在最近几十年中,振动光谱方法(如拉曼和傅里叶变换红外光谱)被广泛应用于研究等离子体和血清样本。这些方法与滴涂沉积技术相结合,可预先浓缩干燥液滴中的生物分子,以提高检测到的振动信号。然而,最常遇到的挑战是由于咖啡环效应导致生物分子的不均匀再分布。在这项研究中,使用拉曼和傅里叶变换红外光谱以及荧光寿命成像方法研究了干燥样品液滴内生物分子的分布变化。研究了来自健康供体的血浆样本,以显示干燥样品液滴的内圈和外圈区域之间的光谱差异。此外,通过使用氘化白蛋白说明了在等离子体干燥过程中血液中最丰富的蛋白质白蛋白的优先沉积位置。随后,对两名患有不同心脏相关疾病的患者进行了示例研究,以说明在干燥过程中血浆和血清生物分子分布的变化及其对患者分层的影响。该研究表明,对于使用振动光谱对患者的血浆和血清样本进行彻底的临床特征描述,有必要对液滴的内外圈进行均匀的采样位置。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74d/7926873/0e9ec0e82df2/ijms-22-02191-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74d/7926873/0524f78d3ed7/ijms-22-02191-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74d/7926873/f1abfc1edc7a/ijms-22-02191-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74d/7926873/72033ed88e23/ijms-22-02191-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74d/7926873/ef97dded8d5e/ijms-22-02191-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74d/7926873/0e9ec0e82df2/ijms-22-02191-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74d/7926873/0524f78d3ed7/ijms-22-02191-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74d/7926873/f1abfc1edc7a/ijms-22-02191-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74d/7926873/72033ed88e23/ijms-22-02191-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74d/7926873/ef97dded8d5e/ijms-22-02191-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a74d/7926873/0e9ec0e82df2/ijms-22-02191-g005.jpg

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