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通过高效液相色谱分析对器官组织样本中的荧光染料进行定量。

Quantification of fluorescent dyes in organ tissue samples via HPLC analysis.

作者信息

Morsbach S, García-Bardon A, Kamuf J, Müller B, Beghersa N, Mohr K, Landfester K

机构信息

Max Planck Institute for Polymer Research, Ackermannweg 10, Mainz, 55128 Germany.

Department of Anesthesiology, Medical Center of the Johannes Gutenberg University, Langenbeckstraße 1, Mainz, 55131 Germany.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Jan 1;1072:34-39. doi: 10.1016/j.jchromb.2017.11.012. Epub 2017 Nov 10.

Abstract

The determination of regional blood flow via the accumulation of fluorescent microspheres is a concept regularly used in medical research. Typically, the microbeads get extracted from the tissue of interest and are then quantified by measuring the absorption or fluorescence of the incorporated dyes without further separation from the medium. However, in that case the absorption spectra of different dyes can overlap when used simultaneously, leading to an overestimation of the concentration. Additionally, background absorption from the medium can be problematic. Therefore, a high performance liquid chromatography method for the simultaneous detection of four dyes (orange, crimson, yellow-green and red) incorporated in different microbeads in samples from biological media such as organ tissue (brain, heart and kidneys) was developed. Since for biological samples often a large sample size is required for sufficient statistics, the method was optimized to yield very short run times. With this method it was possible to detect very low concentrations of only one microsphere per gram of organ tissue. By applying this sensitive quantification technique, it was demonstrated that the application of microbeads for perfusion measurements might not be reliable due to different organ distributions in each animal.

摘要

通过荧光微球积累来测定局部血流是医学研究中经常使用的一个概念。通常,微珠从感兴趣的组织中提取出来,然后通过测量掺入染料的吸收或荧光进行定量,无需与介质进一步分离。然而,在这种情况下,不同染料的吸收光谱在同时使用时可能会重叠,导致浓度高估。此外,介质的背景吸收可能会产生问题。因此,开发了一种高效液相色谱法,用于同时检测生物介质(如器官组织(脑、心脏和肾脏))样本中不同微珠中掺入的四种染料(橙色、深红色、黄绿色和红色)。由于对于生物样本,通常需要较大的样本量才能获得足够的统计数据,因此对该方法进行了优化,以实现非常短的运行时间。使用这种方法,可以检测到每克器官组织中极低浓度的仅一种微球。通过应用这种灵敏的定量技术,结果表明,由于每只动物中微珠的器官分布不同,使用微珠进行灌注测量可能不可靠。

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