Ri. Stefan et al., Maltodextrins as new chiral selectors in the design of potentiometric, enantioselective membrane electrodes, FRESEN J AN, 370(1), 2001, pp. 33-37
Maltodextrins (dextrose equivalent (DE) 4.0-7.0, 13.0-17.0, and 16.5-19.5)
are proposed as novel chiral selectors for the construction of potentiometr
ic, enantioselective membrane electrodes. The potentiometric, enantioselect
ive membrane electrodes can be used reliably for the assay of S-captopril a
s raw material and in pharmaceutical formulations such as Novocaptopril tab
lets, by use of direct potentiometry. The best response was obtained when m
altodextrin with higher DE was used for construction of the electrode. The
best enantioselectivity and time-stability was achieved for the lower DE ma
ltodextrin. L-proline was found to be the main interferent for all the prop
osed electrodes. The surface of the electrodes can be regenerated by simply
polishing; this furnishes a fresh surface ready for use in a new assay.