Jr. Veraart et al., Non-aqueous capillary electrophoresis of biological samples after at-line solid-phase extraction, CHROMATOGR, 52(7-8), 2000, pp. 408-412
Solid-phase extraction (SPE) wets coupled at-line to capillary electrophore
sis (CE) for the determination of a series of basic lest compounds (i.e. tr
icyclic antidepressants). The analysis was performed using a non-aqueous CE
buffer, which resulted in baseline separation of all test compounds. This
is in marked contrast with CE using aqueous buffers where hardly any separa
tion was obtained either with or without micelles. The SPE procedure was us
ed to remove simultaneously most of the water from the sample, because no d
irect analysis of aqueous samples is possible when a non-aqueous CE buffer
is used. With the present method the antidepressants can be determined in b
oth urine and serum. Analyte detectability is increased up to to-fold due t
o trace enrichment during the extraction process the limits of detection (L
ODs; UV 214 nm) are 30 - 300 ng mL(-1) in urine and 300 - 1000 ng mL(-1) in
serum. The RSD values (n = 5) of the within-day and between-day precision
are below 9% and 11%, respectively. Therefore, the present procedure can be
used for drug monitoring.