University of Exeter, School of Physics and Astronomy, Exeter, United Kingdom.
M Squared Lasers Ltd., Glasgow, United Kingdom.
J Biomed Opt. 2020 Jun;25(6):1-7. doi: 10.1117/1.JBO.25.6.066502.
Stimulated Raman scattering (SRS) and pump-probe microscopy are implementations of multiphoton microscopy that acquire high-resolution, label-free images of live samples encoded with molecular contrast. Most commercial multiphoton microscopes cannot access these techniques since they require sample illumination by two temporally synchronized ultrafast pulse trains. We present a compact and robust way of synchronizing an additional Ti:sapphire laser with a conventional single-beam multiphoton microscope to realize an instrument that can acquire images with enhanced molecular specificity.
A passive optical synchronization scheme for a pair of commercially available, unmodified modelocked Ti:sapphire lasers was developed. The suitability of this synchronization scheme for advanced biomedical microscopy was investigated.
A pair of modelocked Ti:sapphire lasers were aligned in master-slave configuration. Five percent of the master laser output was used to seed the modelocking in the slave laser cavity. The timing jitter of the master and slave pulse trains was characterized using an optical autocorrelator. The synchronized output of both lasers was coupled into a laser scanning microscope and used to acquire spectral focusing SRS and pump-probe microscopy images from biological and nonbiological samples.
A timing jitter between the modelocked pulse trains of 0.74 fs was recorded. Spectral focusing SRS allowed spectral discrimination of polystyrene and polymethyl methacrylate beads. Pump-probe microscopy was used to record excited state lifetime curves from hemoglobin in intact red blood cells.
Our work demonstrates a simple and robust method of upgrading single-beam multiphoton microscopes with an additional ultrafast laser. The resulting dual-beam instrument can be used to acquire label-free images of sample structure and composition with high biochemical specificity.
受激拉曼散射 (SRS) 和泵浦探测显微镜是多光子显微镜的实现方式,可对具有分子对比度的活样本进行高分辨率、无标记的成像。大多数商业多光子显微镜无法使用这些技术,因为它们需要两个时间同步的超快脉冲串对样品进行照明。我们提出了一种紧凑而强大的方法,可以将额外的钛宝石激光器与传统的单光束多光子显微镜同步,从而实现可以获取具有增强分子特异性的图像的仪器。
开发了一种商用、未经修改的锁模钛宝石激光器对的被动光学同步方案。研究了这种同步方案对先进生物医学显微镜的适用性。
将一对锁模钛宝石激光器以主从配置对齐。使用主激光器输出的 5%来种子从激光器腔中的锁模。使用光学自相关器对主脉冲串和从脉冲串的定时抖动进行了表征。将同步后的两个激光器的输出耦合到激光扫描显微镜中,并用于从生物和非生物样本中获取光谱聚焦受激拉曼散射和泵浦探测显微镜图像。
记录到锁模脉冲串之间的定时抖动为 0.74 fs。光谱聚焦受激拉曼散射允许对聚苯乙烯和聚甲基丙烯酸甲酯珠进行光谱分辨。泵浦探测显微镜用于记录完整红细胞中血红蛋白的激发态寿命曲线。
我们的工作展示了一种简单而强大的方法,可通过额外的超快激光器对单光束多光子显微镜进行升级。由此产生的双光束仪器可用于获取具有高生化特异性的样本结构和组成的无标记图像。