Lowering the UV absorbance detection limit and increasing the sensitivity of capillary electrophoresis using a dual linear photodiode array detector and signal averaging
Ct. Culbertson et Jw. Jorgenson, Lowering the UV absorbance detection limit and increasing the sensitivity of capillary electrophoresis using a dual linear photodiode array detector and signal averaging, J MICROCOL, 11(9), 1999, pp. 652-662
We have recently described a new spatial signal-averaging approach to impro
ve the UV absorbance detection limits for capillary electrophoresis (CE) us
ing a single photodiode array (PDA) detector. (Culbertson, C. T.; Jorgenson
, J. W. Anal Chem 1998 70, 2629: Culbertson, C. T. PhD Dissertation, Univer
sity of North Carolina, Chapel Kill, 1996). At low analyte concentrations,
however, source flicker noise interfered with the signal-averaging process.
This noise was due to inadequate compensation of the spatial and temporal
lamp fluctuations that occurred over the course of a run in this single-bea
m instrument. To better compensate for the source lamp fluctuations and dri
ft, a double-beam detector has been constructed using a dual PDA to continu
ously monitor the output of the source. The addition of the reference chann
el significantly reduces the source flicker noise. To demonstrate the capab
ilities of this new detector, separations of four nucleic acids at six diff
erent concentrations were performed. The signal-averaged electropherograms
generated using the double-beam instrument are compared with electropherogr
ams obtained from individual diodes in the array, a single-beam detector, a
nd a commercial single-point detector. The detection limits for the double-
beam instrument were 35(+/- 3) times better than that obtained using an ind
ividual diode in the array, ca. 4 times better than that obtained using a s
ingle-beam detector, and 6.3(+/- 0.4) times better than that obtained using
a commercial single-point detector. The linearity of the new detector is f
ound to be equal to or better than that of the commercial single-point dete
ctor, and a separation of analytes at mixed concentrations corresponding to
a two order of magnitude dynamic range is shown. (C) 1999 John Wiley & Son
s, Inc.