University of Alberta, Department of Electrical and Computer Engineering, Edmonton, Alberta, T6G 2V4, Canada.
J Biomed Opt. 2012 Jul;17(7):076024. doi: 10.1117/1.JBO.17.7.076024.
We present a new integrated micro-endoscopy system combining label-free, fiber-based, real-time C-scan optical-resolution photoacoustic microscopy (F-OR-PAM) and a high-resolution fluorescence micro-endoscopy system for visualizing fluorescently labeled cellular components and optically absorbing microvasculature simultaneously. With a diode-pumped 532-nm fiber laser, the F-OR-PAM sub-system is able to reach a resolution of ∼7 μm. The fluorescence subsystem, which does not require any mechanical scanning, consists of a 447.5-nm-centered diode laser as the light source, an objective lens, and a CCD camera. Proflavine is used as the fluorescent contrast agent by topical application. The scanning laser and the diode laser light source share the same light path within an optical fiber bundle containing 30,000 individual single-mode fibers. The absorption of proflavine at 532 nm is low, which mitigates absorption bleaching of the contrast agent by the photoacoustic excitation source. We demonstrate imaging in live murine models. The system is able to provide cellular morphology with cellular resolution co-registered with the structural information given by F-OR-PAM. Therefore, the system has the potential to serve as a virtual biopsy technique, helping visualize angiogenesis and the effects of anti-cancer drugs on both cells and the microcirculation, as well as aid in the study of other diseases.
我们提出了一种新的集成微内窥镜系统,结合了无标记、基于光纤的实时 C 扫描光分辨率光声显微镜(F-OR-PAM)和高分辨率荧光微内窥镜系统,用于同时可视化荧光标记的细胞成分和光吸收的微血管。使用二极管泵浦 532nm 光纤激光,F-OR-PAM 子系统能够达到 ∼7μm 的分辨率。荧光子系统不需要任何机械扫描,由中心波长为 447.5nm 的二极管激光器、物镜和 CCD 相机组成。吖啶黄被用作局部应用的荧光对比剂。扫描激光和二极管激光光源共享包含 30000 根单模光纤的光纤束内的同一路径。吖啶黄在 532nm 处的吸收较低,减轻了光声激发源对对比剂的吸收漂白。我们在活体小鼠模型中进行了成像演示。该系统能够以细胞分辨率提供细胞形态学成像,并与 F-OR-PAM 提供的结构信息进行配准。因此,该系统有可能作为一种虚拟活检技术,帮助可视化血管生成以及抗癌药物对细胞和微循环的影响,并有助于研究其他疾病。