Hadamard transform microchip electrophoresis combined with laser-induced fluorescence detection using a compact neodymium-doped yttrium aluminum garnet laser emitting at 532 nm

被引:5
作者
Hata, Kazuki [1 ]
Kaneta, Takashi [2 ,3 ]
Imasaka, Totaro [2 ,3 ]
机构
[1] Kyushu Univ, Grad Sch Engn, Dept Appl Chem, Fukuoka 8190395, Japan
[2] Kyushu Univ, Ctr Future Chem, Grad Sch Engn, Dept Appl Chem, Fukuoka 8190395, Japan
[3] Kyushu Univ, Ctr Future Chem, Div Translat Res, Fukuoka 8190395, Japan
关键词
biochemistry; bioMEMS; chemical variables measurement; dyes; electrophoresis; fluorescence; Hadamard transforms; lab-on-a-chip; light sources; measurement by laser beam; microfluidics; molecular biophysics; S-matrix theory; CAPILLARY-ZONE-ELECTROPHORESIS; ELECTROCHEMICAL DETECTION; INJECTION; SHAH; FLUOROMETRY; SEPARATION; PROTEINS; DEVICES;
D O I
10.1063/1.3116121
中图分类号
O59 [应用物理学];
学科分类号
摘要
Hadamard transform electrophoresis combined with laser-induced fluorescence (LIF) detection on a microchip was demonstrated. A compact, diode-pumped neodymium-doped yttrium aluminum garnet laser was employed as the light source for LIF detection. The analytical conditions were optimized using rhodamine B as the analyte. Under optimal conditions, the signal-to-noise ratio (S/N) of the analyte was improved by a factor of 7.5 by means of Hadamard transformation based on a 255-order cyclic S matrix. Additionally, the relationship between fluorescence intensity and analyte concentration was linear with a correlation coefficient of 0.993 in the inverse Hadamard transformed data at the concentration range from 25 to 100 pM. The results indicate that the present method is applicable to quantitative analysis at the concentration lower than the concentration limit of detection in a conventional method. The concentration limit of detection was similar to 25 pM (the relative standard deviation of the peak height was 5.2%). The present technique was successfully applied to the separation of a mixture containing 1.9 nM phenylalanine and 1.9 nM glutamic acid labeled with rhodamine B isothiocyanate. The S/Ns of the analyte peaks were improved up to similar to 10 in the inverse Hadamard transformed data derived from a 127-order cyclic S matrix, while neither peak was lower than the limit of detection (S/N < 3) in conventional microchip electrophoresis by a single injection.
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页数:6
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