Karpf Sebastian, Eibl Matthias, Sauer Benjamin, Reinholz Fred, Hüttmann Gereon, Huber Robert
Lehrstuhl für BioMolekulare Optik, Fakultät für Physik, Ludwig-Maximilians-Universität München, Oettingenstr. 67, 80538 Munich, Germany; Department of Electrical Engineering, University of California, Los Angeles, California 90095, USA.
Institut für Biomedizinische Optik, Universität zu Lübeck, Peter-Monnik-Weg 4, 23562 Lübeck, Germany.
Biomed Opt Express. 2016 Jun 1;7(7):2432-40. doi: 10.1364/BOE.7.002432. eCollection 2016 Jul 1.
Two-photon excitation fluorescence (TPEF) microscopy is a powerful technique for sensitive tissue imaging at depths of up to 1000 micrometers. However, due to the shallow penetration, for in vivo imaging of internal organs in patients beam delivery by an endoscope is crucial. Until today, this is hindered by linear and non-linear pulse broadening of the femtosecond pulses in the optical fibers of the endoscopes. Here we present an endoscope-ready, fiber-based TPEF microscope, using nanosecond pulses at low repetition rates instead of femtosecond pulses. These nanosecond pulses lack most of the problems connected with femtosecond pulses but are equally suited for TPEF imaging. We derive and demonstrate that at given cw-power the TPEF signal only depends on the duty cycle of the laser source. Due to the higher pulse energy at the same peak power we can also demonstrate single shot two-photon fluorescence lifetime measurements.
双光子激发荧光(TPEF)显微镜是一种强大的技术,可用于对深度达1000微米的组织进行灵敏成像。然而,由于穿透深度较浅,对于患者体内器官的成像而言,通过内窥镜进行光束传输至关重要。直到如今,这一过程受到内窥镜光纤中飞秒脉冲的线性和非线性脉冲展宽的阻碍。在此,我们展示了一种基于光纤的、可用于内窥镜的TPEF显微镜,它使用低重复率的纳秒脉冲而非飞秒脉冲。这些纳秒脉冲不存在与飞秒脉冲相关的大多数问题,但同样适用于TPEF成像。我们推导并证明,在给定的连续波功率下,TPEF信号仅取决于激光源的占空比。由于在相同峰值功率下具有更高的脉冲能量,我们还能够展示单次双光子荧光寿命测量。