研究目的
Investigating the use of an ultrashort pulse laser for two-photon phase-resolved fluorescence-lifetime measurement to facilitate high-speed measurement of fluorescence lifetimes of biological samples.
研究成果
The proposed two-photon phase-resolved fluorescence-lifetime measurement method is feasible for accurate measurement of fluorescence lifetimes, as validated by measurements on rhodamine B and a cellular thermoprobe. The method offers potential for high-speed measurement of biological samples with minimal equipment requirements.
研究不足
The study assumes monoexponential fluorescence decay in all cases, which may not hold for all samples. The method's applicability to samples with complex decay kinetics is not explored.
1:Experimental Design and Method Selection:
The study employs a two-photon phase-resolved fluorescence-lifetime measurement method using an ultrashort pulse laser and a lock-in amplifier.
2:Sample Selection and Data Sources:
Rhodamine B and a cellular thermoprobe were used as samples.
3:List of Experimental Equipment and Materials:
A titanium–sapphire laser, photomultipliers (PMT 1 and PMT 2), a lock-in amplifier, and a short-pass filter were used.
4:Experimental Procedures and Operational Workflow:
The laser irradiates the sample, and fluorescence signals are detected by PMT 2, with PMT 1 detecting the excitation signal. The lock-in amplifier combines these signals to measure the phase difference.
5:Data Analysis Methods:
The fluorescence lifetime is calculated based on the phase difference between the reference and fluorescence signals.
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