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首页> 外文期刊>Journal of biomedical optics >Two-photon excited fluorescence enhancement with broadband versus tunable femtosecond laser pulse excitation
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Two-photon excited fluorescence enhancement with broadband versus tunable femtosecond laser pulse excitation

机译:宽带双光子激发荧光增强与可调谐飞秒激光脉冲激发

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The inverse relationship between two-photon excited fluorescence (TPEF) and laser pulse duration suggests that two-photon microscopy (TPM) performance may be improved by decreasing pulse duration. How ever, for ultrashort pulses of sub-10 femtosecond (fs) in duration, its spectrum contains the effective gain bandwidth of Ti:Sapphire and its central wavelength is no longer tunable. An experimental study was performed to explore this apparent tradeoff between untuned sub-10 fs transform-limited pulse (TLP) and tunable 140 fs pulse for TPEF. Enhancement factors of 1.6, 6.7, and 5.2 are measured for lndo-1, FITC, and TRITC excited by sub-10 fs TLP compared with 140 fs pulse tuned to the two-photon excitation (TPE) maxima at 730 nm, 800 nm, and 840 nm, respectively. Both degenerate (v_1 = v_2) and nondegenerate (v_1≠v_2) mixing of sub-10 fs TLP spectral components result in its broad second-harmonic (SH) power spectrum and high spectral density, which can effectively compensate for the lack of central wavelength tuning and lead to large overlap with dye TPE spectra for TPEF enhancements. These pulse properties were also exploited for demonstrating its potential applications in multicolor imaging with TPM.
机译:双光子激发荧光(TPEF)与激光脉冲持续时间之间的反比关系表明,可以通过减少脉冲持续时间来改善双光子显微镜(TPM)性能。但是,对于持续时间小于10飞秒(fs)的超短脉冲,其频谱包含有效的Ti:Sapphire增益带宽,并且其中心波长不再可调。进行了一项实验研究,以探索未调谐的低于10 fs的变换限制脉冲(TLP)与TPEF的可调140 fs脉冲之间的这种明显折衷。对于通过sub-10 fs TLP激发的lndo-1,FITC和TRITC,测量了1.6、6.7和5.2的增强因子,而将140 fs脉冲调谐到730 nm,800 nm的双光子激发(TPE)最大值,则增强因子为1.6、6.7和5.2。和840 nm。次10 fs TLP光谱分量的简并(v_1 = v_2)和非简并(v_1≠v_2)混合导致其宽泛的二次谐波(SH)功率谱和高光谱密度,可有效补偿中心波长的不足调整并导致与染料TPE光谱的大量重叠以增强TPEF。这些脉冲特性也被用于证明其在TPM多色成像中的潜在应用。

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