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The ion-channel sensor technique was used to determine heparin concentrations in artifcial and horse serum with cyclic voltammetry. The sensor is based on self-assembled monolayers (SAMs) of thioctic acid on which rotamine is attached as a receptor to control the rate of [Mo(CN)8]4− oxidation or [Fe(CN)6]3− reduction in the presence of heparin. The analyte, heparin, with its negative charges, neutralizes the ositive charges on the rotamine receptor and at high heparin concentrations provides the electrode surface with an excess of negative charge, thereby repulsing the marker ions from the electrode surface. This decreases the redox currents and makes them a function of the analyte concentration. In artificial serum, a linear concentration range of 0.05–1.5 mg/ml was obtained for the heparin response at a scan rate of 10.24 V/s when [Mo(CN)8]4−was used as marker. Repeated measurements of heparin in artifcial and horse serum gave average heparin concentrations of 1.30 and 1.56 mg/ml, respectively, compared to 1.25 mg/ml heparin that was introduced into the serum. Measurements of heparin in horse serum using a fresh electrode for each sample, however, gave an average heparin concentration of 1.21mg/ml with a standard deviation of 0.026 mg/ml. © 2000 Elsevier Science B.V. All rights reserved |
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