The analysis of donepezil, a centrally acting acetylcholine esterase inhibi
tor, is described by a CZE method suitable for applications in pharmaceutic
al held. A rapid migration of the analyte was obtained under acidic conditi
ons (pH 3.0); with detection wavelength of 320 nm a LOD of 0.8 x 10(-3) mg/
ml was provided. Applications on real sample (pharmaceuticals) were carried
out using two different instruments with comparable results in terms of re
producibility and accuracy, The use of chiral selectors in the running buff
er allowed the enantioseparation of donepezil; charged cyclodextrins (carbo
xymethyl-beta -cyclodextrin and sulfated-beta -cyclodextrin) were suitable
for the chiral resolution of the analyte, Interesting results were also obt
ained using human serum albumin. The protein-based CE enantioseparation was
carried out at pH 7.4 avoiding the partial filling technique due to the go
od absorptivity of donepezil at 320 nm. Interestingly, the use of bicine as
BGE provided a significative improvement in the enantioresolution compared
to that obtained by phosphate buffer. (C) 2001 Elsevier Science B.V. All r
ights reserved.