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Accurate histopathology from low signal-to-noise ratio spectroscopic imaging data.从低信噪比波谱成像数据中获取准确的组织病理学信息。
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Resonant Mie scattering in infrared spectroscopy of biological materials--understanding the 'dispersion artefact'.生物材料红外光谱中的共振米氏散射——理解“色散伪像”。
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评估光谱细胞病理学的不同固定方案,第 1 部分。

Evaluating different fixation protocols for spectral cytopathology, part 1.

机构信息

Department of Chemistry & Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts, USA.

出版信息

Anal Chem. 2012 Feb 7;84(3):1259-66. doi: 10.1021/ac202046d. Epub 2012 Jan 24.

DOI:10.1021/ac202046d
PMID:22103764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3277680/
Abstract

Spectral cytopathology (SCP) is a novel approach for disease diagnosis that utilizes infrared spectroscopy to interrogate the biochemical components of cellular samples and multivariate statistical methods, such as principal component analysis, to analyze and diagnose spectra. SCP has taken vast strides in its application for disease diagnosis over the past decade; however, fixation-induced changes and sample handling methods are still not systematically understood. Conversely, fixation and staining methods in conventional cytopathology, typically involving protocols to maintain the morphology of cells, have been documented and widely accepted for nearly a century. For SCP, fixation procedures must preserve the biochemical composition of samples so that spectral changes significant to disease diagnosis are not masked. We report efforts to study the effects of fixation protocols commonly used in traditional cytopathology and SCP, including fixed and unfixed methods applied to exfoliated oral (buccal) mucosa cells. Data suggest that the length of time in fixative and duration of sample storage via desiccation contribute to minor spectral changes where spectra are nearly superimposable. These findings illustrate that changes influenced by fixation are negligible in comparison to changes induced by disease.

摘要

光谱细胞病理学(SCP)是一种新的疾病诊断方法,它利用红外光谱来检测细胞样本的生化成分,并使用主成分分析等多元统计方法来分析和诊断光谱。在过去的十年中,SCP 在疾病诊断中的应用取得了巨大的进展;然而,固定诱导的变化和样本处理方法仍未得到系统的理解。相反,传统细胞病理学中的固定和染色方法通常涉及保持细胞形态的方案,已经记录并被广泛接受了近一个世纪。对于 SCP,固定程序必须保留样本的生化组成,以免掩盖对疾病诊断有重要意义的光谱变化。我们报告了研究传统细胞病理学和 SCP 中常用固定方案的影响的努力,包括应用于脱落口腔(颊)黏膜细胞的固定和未固定方法。数据表明,固定剂中的时间长度和通过干燥储存样品的时间会导致光谱发生微小变化,几乎可以完全重叠。这些发现表明,与疾病引起的变化相比,固定引起的变化可以忽略不计。