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Macrocyclic Antibiotics as Chiral Selectors in the Design of Enantioselective, Potentiometric Membrane Electrodes
Two enantioselective, potentiometric membrane electrodes, based on macrocyclic glycopeptide antibiotics-vancomycin and teicoplanin-were designed. Acetyl-L-carnitine was selected as model analyte. The linear concentration ranges for the proposed electrodes were 10 −5 -10 −2 mol L −1 for the vancomyc...
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Published in: | Instrumentation science & technology 2004-12, Vol.32 (6), p.601-610 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Two enantioselective, potentiometric membrane electrodes, based on macrocyclic glycopeptide antibiotics-vancomycin and teicoplanin-were designed. Acetyl-L-carnitine was selected as model analyte. The linear concentration ranges for the proposed electrodes were 10
−5
-10
−2
mol L
−1
for the vancomycin-based electrode and 10
−4
-10
−2
mol L
−1
for the teicoplanin-based electrode, with slopes of 58.1 and 55.0 mV/p (acetyl-L-carnitine), respectively. The enantioselectivity was determined over D-carnitine. The surfaces of the electrodes are easily renewable by polishing on alumina paper. |
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ISSN: | 1073-9149 1525-6030 |
DOI: | 10.1081/CI-200037017 |