State Key Laboratory of Transducer Technology, Aerospace Information Research Institute, Chinese Academy of Sciences, Beijing, 100190, China.
School of Electronic, Electrical, and Communication Engineering, University of Chinese Academy of Sciences, Beijing, 100049, China.
Anal Bioanal Chem. 2024 Nov;416(26):5815-5825. doi: 10.1007/s00216-024-05509-0. Epub 2024 Aug 30.
The preparation of histology slides is a critical step in histopathology, and poor-quality histology slides with weak adhesion of tissue sections to the substrate often affect diagnostic accuracy and sometimes lead to diagnostic failure due to tissue section detachment. This issue has been of concern and some methods have been proposed to enhance tissue-substrate adhesion. Unfortunately, quantitative analysis of the adhesion between tissue sections and glass slides is still challenging. In this work, the adhesion of mouse brain tissue sections on gold-coated glass slides was analyzed using a laboratory-fabricated hyperspectral surface plasmon resonance microscopy (HSPRM) system that enabled single-pixel spectral SPR sensing and provided two-dimensional (2D) distribution of resonance wavelengths (RWs). The existence of the nanoscale water gap between the tissue section and the substrate was verified by fitting the RW measured in each pixel using the five-layer Fresnel reflection model. In addition, a 2D image of the tissue-substrate adhesion distance (AD) was obtained from the measured 2D distribution of RWs. The results showed that tissue-substrate AD was 20-35 nm in deionized water and 4-24 nm in saline solution. The HSPRM system used in this work has a wide wavelength range of 400-1000 nm and can perform highly sensitive and label-free detection over a large dynamic detection range with high spectral and spatial resolutions, showing significant potential applications in stain-free tissue imaging, quantitative analysis of tissue-substrate adhesion, accurate identification of tumor cells, and rapid histopathological diagnosis.
组织学切片的制备是组织病理学中的一个关键步骤,而组织切片与载玻片之间附着力差、质量差的组织学切片往往会影响诊断的准确性,有时甚至会导致由于组织切片脱落而导致诊断失败。这个问题一直备受关注,已经提出了一些方法来增强组织与载玻片之间的附着力。不幸的是,定量分析组织切片与玻璃载玻片之间的附着力仍然具有挑战性。在这项工作中,使用实验室制作的超光谱表面等离子体共振显微镜(HSPRM)系统分析了小鼠脑组织切片在镀金玻璃载玻片上的附着力,该系统能够实现单像素光谱 SPR 传感,并提供共振波长(RW)的二维(2D)分布。通过使用五层菲涅尔反射模型拟合每个像素测量的 RW,验证了组织切片与基底之间存在纳米级水隙。此外,还可以从测量的 RW 的二维分布中获得组织-基底附着距离(AD)的二维图像。结果表明,在去离子水中组织-基底 AD 为 20-35nm,在盐溶液中为 4-24nm。本工作中使用的 HSPRM 系统具有 400-1000nm 的宽波长范围,能够在具有高光谱和空间分辨率的大动态检测范围内进行高灵敏度和无标记检测,在无染色组织成像、组织-基底附着力的定量分析、肿瘤细胞的准确识别和快速组织病理学诊断等方面具有显著的应用潜力。