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   <subfield code="a">Voltammetric detection of guanosine and adenosine using a carbon paste electrode modified with 1-ethyl-3-methylimidazolium ethylsulfate</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Hongwei Gao, Yuanyuan Duan, Mengying Xi, Wei Sun]</subfield>
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   <subfield code="a">A novel kind of carbon paste electrode (CPE) was prepared by mixing graphite powder, liquid paraffin and the ionic liquid 1-ethyl-3-methylimidazolium ethylsulfate. The resulting electrode was used for the simultaneous determination of guanosine and adenosine by differential pulse voltammetry. Compared to a conventional CPE, the oxidation peak currents are largely increased, and the oxidation peak potentials are negatively shifted. The electrochemical responses to guanosine and adenosine were investigated. Under optimized conditions, the calibration curves are linear in the concentration range from 1.0 × 10-6mol L-1 to 1.6 × 10-4mol L-1 for guanosine, and from 1.0 × 10-6mol L-1 to 2.7 × 10-4mol L-1 for adenosine at pH 3.5. Substances potentially interfering in the biological matrix do no interfere. The method was successfully applied to detect adenosine and guanosine in human urine without sample treatments. Figure Cyclic voltammograms on CPE (a) and CILE (b) for 1.0 × 10-4mol L-1 adenosine and 1.0 × 10-4mol L-1guanosine in a pH 3.5 B-R buffer solution at the scan rate of 100mV s-1. Inset was the typical differential pulse voltammograms of 1.0 × 10-4mol L-1 adenosine and 1.0 × 10-4mol L-1 L guanosine on CILE</subfield>
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   <subfield code="t">Microchimica Acta</subfield>
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