Sun Yun-xu, Zhu Feng, Ma Wan-yun
Key Laboratory for Atomic and Molecular Nanosciences of Education Ministry, Department of Physics, Tsinghua University, Beijing 100084, China.
Guang Pu Xue Yu Guang Pu Fen Xi. 2005 Apr;25(4):502-5.
This paper describes a new method, multiphoton excitation fluorescence detection combined with capillary electrophoresis separation. The excitation source was a self mode-locked femtosecond titanium-sapphire laser (Spectra-physics Inc.), producing a stream of pulses with a pulse duration of about 100 fs at 82 MHz repetition rate. Its average power was about 200 mW at 750 nm. The laser beam was focused into a thin wall flow cell of capillary electrophoresis. A high numerical aperture objective (100 x NA 1.25) was chosen to focus the laser beam and to collect the fluorescence emitted by detecting molecules. Then the fluorescence was detected by a fast response PMT. All data were acquired and processed by a microcomputer. For three biological molecules, 5HT, FAD and NADH, it was demonstrated that they can be separated and detected efficiently by this method with three-photon and two-photon excitation respectively using only one 750 nm laser beam. The detection limits were 1.0 x 10(-6) mol x L(-1) for 5HT, 7.4 x 10(-7) mol x L(-1) for FAD and 9.8 x 10(-7) mol x L(-1) for NADH using the criterion of three standard deviations above background. The results are much better than those with UV absorption detection by one or two magnitudes.
本文描述了一种新方法,即多光子激发荧光检测与毛细管电泳分离相结合。激发源是一台自锁模飞秒钛宝石激光器(光谱物理公司),以82MHz的重复频率产生脉宽约为100fs的脉冲串。其在750nm处的平均功率约为200mW。激光束聚焦到毛细管电泳的薄壁流通池中。选用高数值孔径物镜(100×NA 1.25)来聚焦激光束并收集检测分子发出的荧光。然后通过快速响应光电倍增管检测荧光。所有数据由微型计算机采集和处理。对于三种生物分子5-羟色胺(5HT)、黄素腺嘌呤二核苷酸(FAD)和烟酰胺腺嘌呤二核苷酸(NADH),结果表明仅使用一束750nm激光束,分别通过三光子和双光子激发,该方法就能有效地对它们进行分离和检测。使用高于背景三倍标准差的标准,5HT的检测限为1.0×10⁻⁶mol·L⁻¹,FAD为7.4×10⁻⁷mol·L⁻¹,NADH为9.8×10⁻⁷mol·L⁻¹。结果比紫外吸收检测法好一到两个数量级。