Techna Institute for the Advancement of Technology for Health, University Health Network, Toronto, ON, M5G-1P5, Canada.
Department of Medical Biophysics, University of Toronto, 101 College Street Suite 15-701, Toronto, ON, M5G 1L7, Canada.
Sci Rep. 2017 Mar 28;7(1):468. doi: 10.1038/s41598-017-00272-y.
Spatially Targeted Mass Spectrometry (MS) analysis using survey scans with an imaging modality often requires consecutive tissue slices, because of the tissue damage during survey scan or due to incompatible sample preparation requirements between the survey modality and MS. We report two spatially targeted MS analysis workflows based on polarized light imaging guidance that use the same tissue sample for survey and targeted analysis. The first workflow is applicable for thin-slice analysis, and uses transmission-polarimetry-guided Desorption ElectroSpray Ionization Mass Spectrometry (DESI-MS), and confirmatory H&E histopathology analysis on the same slice; this is validated using quantitative digital pathology methods. The second workflow explores a polarimetry-guided MS platform for thick tissue assessment by developing reflection-mode polarimetric imaging coupled with a hand-held Picosecond InfraRed Laser (PIRL) MS ablation probe that requires minimal tissue removal to produce detectable signal. Tissue differentiation within 5-10 s of sampling with the hand-held probe is shown using multivariate statistical methods of the MS profiles. Both workflows were tasked with differentiating necrotic cancer sites from viable cancers using a breast tumour model, and their performance was evaluated. The use of the same tissue surface addresses mismatches in guidance due to intrinsic changes in tissue morphology over consecutive sections.
基于偏光成像引导的两种空间靶向 MS 分析工作流程,均使用相同的组织样本进行调查和靶向分析。第一个工作流程适用于薄片分析,采用透射偏光引导解吸电喷雾电离质谱(DESI-MS),并在同一切片上进行 H&E 组织病理学分析的验证;该方法通过定量数字病理学方法进行验证。第二个工作流程通过开发反射模式偏光成像,结合手持皮秒红外激光(PIRL)MS 消融探头,探索了一种用于厚组织评估的偏光引导 MS 平台,该平台仅需最小程度的组织去除即可产生可检测信号。使用 MS 谱的多元统计方法显示,手持探头在 5-10 秒内对组织进行采样,可实现组织分化。使用乳腺癌模型对这两种工作流程进行了区分坏死性癌灶与存活性癌灶的任务,并对其性能进行了评估。使用相同的组织表面可以解决由于连续切片中组织形态的固有变化而导致的引导不匹配问题。