多面镜阵列照明器,用于荧光激发-扫描光谱成像显微镜。
Multifaceted mirror array illuminator for fluorescence excitation-scanning spectral imaging microscopy.
机构信息
University of South Alabama, Department of Chemical and Biomolecular Engineering, Mobile, Alabama, United States.
University of South Alabama, Systems Engineering, Mobile, Alabama, United States.
出版信息
J Biomed Opt. 2023 Feb;28(2):026502. doi: 10.1117/1.JBO.28.2.026502. Epub 2023 Feb 7.
SIGNIFICANCE
Hyperspectral imaging (HSI) technologies offer great potential in fluorescence microscopy for multiplexed imaging, autofluorescence removal, and analysis of autofluorescent molecules. However, there are also associated trade-offs when implementing HSI in fluorescence microscopy systems, such as decreased acquisition speed, resolution, or field-of-view due to the need to acquire spectral information in addition to spatial information. The vast majority of HSI fluorescence microscopy systems provide spectral discrimination by filtering or dispersing the fluorescence emission, which may result in loss of emitted fluorescence signal due to optical filters, dispersive optics, or supporting optics, such as slits and collimators. Technologies that scan the fluorescence excitation spectrum may offer an approach to mitigate some of these trade-offs by decreasing the complexity of the emission light path.
AIM
We describe the development of an optical technique for hyperspectral imaging fluorescence excitation-scanning (HIFEX) on a microscope system.
APPROACH
The approach is based on the design of an array of wavelength-dependent light emitting diodes (LEDs) and a unique beam combining system that uses a multifurcated mirror. The system was modeled and optimized using optical ray trace simulations, and a prototype was built and coupled to an inverted microscope platform. The prototype system was calibrated, and initial feasibility testing was performed by imaging multilabel slide preparations.
RESULTS
We present results from optical ray trace simulations, prototyping, calibration, and feasibility testing of the system. Results indicate that the system can discriminate between at least six fluorescent labels and autofluorescence and that the approach can provide decreased wavelength switching times, in comparison with mechanically tuned filters.
CONCLUSIONS
We anticipate that LED-based HIFEX microscopy may provide improved performance for time-dependent and photosensitive assays.
意义
高光谱成像 (HSI) 技术在荧光显微镜中具有很大的应用潜力,可用于多路复用成像、去除自发荧光以及分析自发荧光分子。然而,在荧光显微镜系统中实施 HSI 也存在一些相关的权衡,例如由于需要获取空间信息之外的光谱信息,采集速度、分辨率或视场会降低。绝大多数 HSI 荧光显微镜系统通过滤波或分光来提供光谱分辨,这可能会由于光学滤波器、分光光学元件或支撑光学元件(例如狭缝和准直器)而导致发射荧光信号的损失。扫描荧光激发光谱的技术可能提供一种方法来减轻其中一些权衡,通过降低发射光路的复杂性。
目的
我们描述了一种在显微镜系统上进行高光谱成像荧光激发扫描 (HIFEX) 的光学技术的开发。
方法
该方法基于设计一组波长相关的发光二极管 (LED) 和一个独特的光束组合系统,该系统使用多分叉镜。该系统使用光学光线追踪模拟进行建模和优化,并构建了一个原型并将其耦合到倒置显微镜平台上。对原型系统进行了校准,并通过对多标记幻灯片进行成像来进行初始可行性测试。
结果
我们展示了系统的光学光线追踪模拟、原型、校准和可行性测试的结果。结果表明,该系统至少可以区分六种荧光标记和自发荧光,并且与机械调谐滤波器相比,该方法可以提供较短的波长切换时间。
结论
我们预计基于 LED 的 HIFEX 显微镜可能会为时间相关和光敏感的测定提供更好的性能。