Measuring two-photon microscopy ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting

被引:0
|
作者
Kim, Youngchan [1 ]
Vogel, Steven S. [1 ]
机构
[1] NIAAA, US Natl Inst Hlth, Sect Cellular Biophoton, Lab Mol Physiol, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
multiphoton microscopy; time-correlated single-photon counting; second-harmonic generation; pulse duration; interferometric autocorrelation; EXCITATION CROSS-SECTIONS; MOLECULAR FLUOROPHORES; DISPERSION;
D O I
10.1117/1.JBO.25.1.014516
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Two-photon microscopy (2PM) has revolutionized biomedical imaging by allowing thin optical sectioning in relatively thick biological specimens. Because dispersive microscope components in 2PM, such as objective lens, can alter temporal laser pulse width (typically being broader at the sample plane), for accurate measurements of two-photon absorption properties, it is important to characterize pulse duration at the sample plane. We present a simple modification to a two-photon microscope light path that allows for second-harmonic-generation-based interferometric autocorrelation measurements to characterize ultrafast laser pulse duration at the sample plane using time-correlated single-photon counting (TCSPC). We show that TCSPC can be used as a simple and versatile method to estimate the zero time delay step value between two adjacent ultrafast laser pulses for these measurements. To demonstrate the utility of this modification, we measured the Coherent Chameleon-Ultra II Ti:sapphire laser pulse width at the sample plane using a 10x air, 40x air, or 63x water-immersion objective lens. At 950-nm two-photon excitation, the measured pulse width was 154 +/- 32, 165 +/- 13, and 218 +/- 27 fs (n = 6, mean +/- standard deviation), respectively. (C) The Authors. Published by SPIE under a Creative Commons Attribution 4.0 Unported License.
引用
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页数:9
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