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The performance of enzymatic biosensors based on the immobilization of different enzymes within a carbon nanotubes paste electrode (CNTPE) prepared by dispersion of multi-wall carbon nanotubes (MWNT) and mineral oil is reported in this work. The strong electrocatalytic activity of carbon nanotubes towards the reduction of hydrogen peroxide and quinones and the oxidation of NADH have allowed an effective low-potential amperometric determination of lactate, phenols, catechols and ethanol, in connection with the incorporation of lactate oxidase, polyphenol oxidase and alcohol dehydrogenase/NAD þ , respectively, within the composite matrix. Compared to the analogous enzymatic CPEs, a great enhancement in the response is observed at the enzymatic CNTPEs. Therefore, highly sensitive lactate, phenols, catechols and alcohols biosensors without using any metal or redox mediator can be obtained with this new composite material.

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In this work we summarize the recent activities of our group regarding the analytical performance of a new composite material, the so-called carbon nanotubes paste electrode (CNTPE) obtained by dispersion of multiwall carbon nanotubes in mineral oil. The electrocatalytic properties towards different redox systems, especially those involved in important enzymatic reactions are discussed. Significant shifting in the overpotentials for the oxidation and/or reduction of hydrogen peroxide, NADH, phenol, catechol, dopamine, ascorbic acid, uric acid and hydroquinone are obtained at CNTPE in comparison with the analogous graphite paste electrode (CPE). The usefulness of the electrode as a matrix for immobilizing enzymes is also demonstrated. Highly sensitive and selective glucose quantification is accomplished even without using permselective films or redox mediators. Enzymatic biosensors obtained by incorporation of lactate oxidase, polyphenol oxidase and alcohol dehydrogenase/NAD þ within the composite material have allowed the successful quantification of lactate, phenol, dopamine, catechin and ethanol. The sensitive quantification of traces of oligonucleotides and double stranded calf thymus DNA by adsorptive stripping is reported. The confined DNA layer demonstrated to be stable either in air, acetate or phosphate buffer. The advantages of incorporating copper particles for the quantification of amino acids and albumin is also discussed.