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首页> 外文期刊>Journal of Biophotonics >Highly versatile confocal microscopy system based on a tunable femtosecond Er: fiber source
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Highly versatile confocal microscopy system based on a tunable femtosecond Er: fiber source

机译:基于可调飞秒Er:光纤源的多功能共聚焦显微镜系统

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摘要

The performance of a confocal microscopy setup based on a single femtosecond fiber system is explored over a broad range of pump wavelengths for both linear and nonlinear imaging techniques. First, the benefits of a laser source in linear fluorescence excitation that is continuously tunable over most of the visible spectrum are demonstrated. The influences of subpicosecond pulse durations on the bleaching behavior of typical fluorophores are discussed. We then utilize the tunable near-infrared output of the femtosecond system in connection with a specially designed prism compressor for dispersion control. Pulses as short as 33 fs are measured in the confocal region. As a consequence, 2 mW of average power are sufficient for two-photon microscopy in an organotypic sample from the mouse brain. This result shows great prospect for deep-tissue imaging in the optimum transparency window around 1100 nm. In a third experiment, we prove that our compact setup is powerful enough to exploit even higher-order non-linearities such as three-photon absorption that we use to induce spatially localized photodamage in DNA.
机译:在线性和非线性成像技术的广泛泵浦波长范围内,探索了基于单飞秒光纤系统的共聚焦显微镜设置的性能。首先,证明了激光光源在线性荧光激发中的好处,该线性荧光激发在大多数可见光谱上都可以连续调节。讨论了亚皮秒脉冲持续时间对典型荧光团漂白行为的影响。然后,我们将飞秒系统的可调近红外输出与专门设计的棱镜压缩机配合使用,以进行色散控制。在共聚焦区域测得的脉冲短至33 fs。结果,对于来自小鼠大脑的器官型样本中的双光子显微镜,平均功率为2 mW就足够了。该结果显示了在约1100 nm的最佳透明度窗口中进行深组织成像的广阔前景。在第三个实验中,我们证明了紧凑的设置足够强大,可以利用甚至更高阶的非线性(例如三光子吸收)来诱导DNA中的空间局部光损伤。

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