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反射模式偏振光指导激光质谱法进入人乳腺癌组织的诊断重要区域。

Reflection mode polarimetry guides laser mass spectrometry to diagnostically important regions of human breast cancer tissue.

机构信息

Department of Medical Biophysics, University of Toronto, Toronto, ON, M5G 1L7, Canada.

Princess Margaret Cancer Centre, University Health Network, Toronto, ON, M5G 1L7, Canada.

出版信息

Sci Rep. 2024 Oct 31;14(1):26230. doi: 10.1038/s41598-024-77963-w.

DOI:10.1038/s41598-024-77963-w
PMID:39482347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11527875/
Abstract

To enhance the clinical utility of mass spectrometry (MS), lengthy dwell times on less informative regions of patient specimens (e.g., adipose tissue in breast) must be minimized. Additionally, a promising variant of MS known as picosecond infrared laser MS (PIRL-MS) faces further challenges, namely, lipid contamination when probing adipose tissue. Here we demonstrate on several thick non-sectioned resected human breast specimens (healthy and malignant) that reflection-mode polarimetric imaging can robustly guide PIRL-MS toward regions devoid of significant fat content to (1) avoid signal contamination and (2) shorten overall MS analysis times. Through polarimetric targeting of non-fat regions, PIRL-MS sampling revealed feature-rich spectral signatures including several known breast cancer markers. Polarimetric guidance mapping was enabled by circular degree-of-polarization (DOP) imaging via both Stokes and Mueller matrix polarimetry. These results suggest a potential synergistic hybrid approach employing polarimetry as a wide-field-imaging guidance tool to optimize efficient probing of tissue molecular content using MS.

摘要

为了增强质谱(MS)的临床实用性,必须尽量减少对患者标本(如乳房中的脂肪组织)无信息区域的长时间停留。此外,一种称为皮秒红外激光 MS(PIRL-MS)的很有前途的 MS 变体还面临着进一步的挑战,即在探测脂肪组织时存在脂质污染。在这里,我们在几个厚的非切片切除的人类乳房标本(健康和恶性)上证明,反射模式偏振成像可以稳健地引导 PIRL-MS 进入没有明显脂肪含量的区域,以(1)避免信号污染和(2)缩短整体 MS 分析时间。通过对非脂肪区域进行偏振靶向,PIRL-MS 采样揭示了富含特征的光谱特征,包括几个已知的乳腺癌标志物。偏振靶向映射是通过 Stokes 和 Mueller 矩阵偏振来实现的圆形偏振度(DOP)成像。这些结果表明,一种潜在的协同混合方法可以利用偏振作为宽场成像引导工具,使用 MS 优化组织分子含量的高效探测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe4/11527875/d29ffe17fbc3/41598_2024_77963_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe4/11527875/b2830bceb6b5/41598_2024_77963_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe4/11527875/8beef12fd98d/41598_2024_77963_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe4/11527875/5717565616ce/41598_2024_77963_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe4/11527875/e81da8091c2a/41598_2024_77963_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe4/11527875/d29ffe17fbc3/41598_2024_77963_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe4/11527875/b2830bceb6b5/41598_2024_77963_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe4/11527875/8beef12fd98d/41598_2024_77963_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe4/11527875/5717565616ce/41598_2024_77963_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe4/11527875/e81da8091c2a/41598_2024_77963_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/efe4/11527875/d29ffe17fbc3/41598_2024_77963_Fig5_HTML.jpg

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