Department of Biomedical Engineering Davis, University of California, Davis, California 95616, USA.
J Biophotonics. 2012 Jan;5(1):14-9. doi: 10.1002/jbio.201100070. Epub 2011 Nov 2.
This paper presents an endoscopic configuration for measurements of tissue autofluorescence using two-photon excitation and time-correlated single photon counting detection through a double-clad photonic crystal fiber (DC-PCF) without pre-chirping of laser pulses. The instrument performance was evaluated by measurements of fluorescent standard dyes, biological fluorophores (collagen and elastin), and tissue specimens (muscle, cartilage, tendon). Current results demonstrate the ability of this system to accurately retrieve the fluorescence decay profile and lifetime of these samples. This simple setup, which offers larger penetration depth than one-photon-based techniques, may be combined with morphology-yielding techniques such as photoacoustic and ultrasound imaging.
本文提出了一种内窥镜配置,用于使用双包层光子晶体光纤(DC-PCF)通过双光子激发和时间相关的单光子计数检测来测量组织自发荧光,而无需预先对激光脉冲进行啁啾。通过测量荧光标准染料、生物荧光团(胶原蛋白和弹性蛋白)和组织标本(肌肉、软骨、肌腱)来评估仪器性能。目前的结果表明,该系统能够准确地恢复这些样品的荧光衰减曲线和寿命。与基于单光子的技术相比,这种具有更大穿透深度的简单设置可以与产生形态的技术(如光声和超声成像)相结合。