Sun Yinghua, Phipps Jennifer, Elson Daniel S, Stoy Heather, Tinling Steven, Meier Jeremy, Poirier Brian, Chuang Frank S, Farwell D Gregory, Marcu Laura
Department of Biomedical Engineering, University of California-Davis, NSF Center for Biophotonics Science and Technology, Davis, CA 95616, USA.
Opt Lett. 2009 Jul 1;34(13):2081-3. doi: 10.1364/ol.34.002081.
A compact clinically compatible fluorescence lifetime imaging microscopy (FLIM) system was designed and built for intraoperative disease diagnosis and validated in vivo in a hamster oral carcinogenesis model. This apparatus allows for the remote image collection via a flexible imaging probe consisting of a gradient index objective lens and a fiber bundle. Tissue autofluorescence (337 nm excitation) was imaged using an intensified CCD with a gate width down to 0.2 ns. We demonstrate a significant contrast in fluorescence lifetime between tumor (1.77+/-0.26 ns) and normal (2.50+/-0.36 ns) tissues at 450 nm and an over 80% intensity decrease at 390 nm emission in tumor versus normal areas. The time-resolved images were minimally affected by tissue morphology, endogenous absorbers, and illumination. These results demonstrate the potential of FLIM as an intraoperative diagnostic technique.
设计并构建了一种紧凑的临床兼容型荧光寿命成像显微镜(FLIM)系统,用于术中疾病诊断,并在仓鼠口腔癌发生模型中进行了体内验证。该仪器允许通过由梯度折射率物镜和光纤束组成的柔性成像探头进行远程图像采集。使用门宽低至0.2 ns的增强型电荷耦合器件对组织自发荧光(337 nm激发)进行成像。我们证明,在450 nm处,肿瘤组织(1.77±0.26 ns)和正常组织(2.50±0.36 ns)之间的荧光寿命存在显著差异,且肿瘤区域与正常区域相比,在390 nm发射处强度降低超过80%。时间分辨图像受组织形态、内源性吸收剂和照明的影响最小。这些结果证明了FLIM作为一种术中诊断技术的潜力。