Abstract: Electrochemical sensors demonstrating enantioselectivity to tryptophan enantiomers, with high selectivity and sensitivity, were fabricated by the use of a monolithic fiber of molecularly imprinted polymer-carbon composite. The recognition mechanism and performance of these sensors were evaluated by differential pulse anodic stripping voltammetry. The sensor imprinted for l-tryptophan not only discriminated the target from its analogues and other amino acids but also responded specifically in racemic mixture in aqueous, biological, and pharmaceutical samples. The binding kinetics of l-tryptophan was also established with the help of anodic stripping cyclic voltammetry and chronocoulometry. The detection limit for l-tryptophan was as low as 0.24ángámL-1 (signal/noiseá=á3) which is appropriate for biomarking diseases, caused by an acute tryptophan-depletion, in clinical setting
Template and target information: l-tryptophan
Author keywords: enantioselectivity, Molecularly imprinted polymer-carbon composite, Fiber sensor, Differential pulse anodic stripping voltammetry, l- and d-Tryptophan