HIGH TEMPORAL RESOLUTION MONITORING OF GLUTAMATE AND ASPARTATE IN-VIVO USING MICRODIALYSIS ONLINE WITH CAPILLARY ELECTROPHORESIS WITH LASER-INDUCED FLUORESCENCE DETECTION
Mw. Lada et al., HIGH TEMPORAL RESOLUTION MONITORING OF GLUTAMATE AND ASPARTATE IN-VIVO USING MICRODIALYSIS ONLINE WITH CAPILLARY ELECTROPHORESIS WITH LASER-INDUCED FLUORESCENCE DETECTION, Analytical chemistry, 69(22), 1997, pp. 4560-4565
An automated method for high temporal resolution monitoring of the neu
rotransmitters glutamate and aspartate in vivo using capillary electro
phoresis (CE) with laser-induced fluorescence (LIF) detection was deve
loped. Microdialysis probes placed in the striatum of anesthetized rat
s were coupled on-line with the CE system by an automated flow-gated i
nterface. Analytes were derivatized on-line with o-phthaldialdehyde/be
ta-mercaptoethanol and detected by LIF using the 354 nm line (7 mW) of
a He-Cd laser for excitation. With dialysis now rates of 1.2 mu L/min
, the detection limit at the dialysis probe was 200 nM for glutamate a
nd aspartate. Glutamate and aspartate could be resolved in less than 5
s with over 200 000 theoretical plates. The sampling time was limited
by the separation time while the temporal resolution was limited to s
imilar to 12 s because of band broadening that occurs within the probe
and its associated tubing. The high temporal resolution allowed the f
irst simultaneous monitoring of glutamate and aspartate overflow durin
g acute electrical stimulation in the rat brain.