Maltodextrins as new chiral selectors in the design of potentiometric, enantioselective membrane electrodes

Citation
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
Citations number
24
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY
ISSN journal
09370633 → ACNP
Volume
370
Issue
1
Year of publication
2001
Pages
33 - 37
Database
ISI
SICI code
0937-0633(200105)370:1<33:MANCSI>2.0.ZU;2-7
Abstract
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.