Department of Materials Science, University of Patras, 26504 Rio Patras, Greece, Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, 48 Vass. Constantinou Avenue, 116 35 Athens, Greece, Institut de Biologie Moleculaire et Cellulaire, UPR9021 CNRS, Immunologie et Chimie Therapeutiques, 67084 Strasbourg, France, and Dipartimento di Scienze Farmaceutiche, Universita di Trieste, Piazzale Europa 1, 34127 Trieste, Italy

Chemistry of Carbon Nanotubes

First-generation glucose biosensors relied on the use of the natural oxygen cosubstrate and the production and detection of hydrogen peroxide and were much simpler, especially when miniaturized sensors are concerned. More sophisticated bioelectronic systems for enhancing the electrical response, based on patterned monolayer or multilayer assemblies and organized enzyme networks on solid electrodes, have been developed for contacting GOx with the electrode support. Electrochemical biosensors are well suited for satisfying the needs of personal (home) glucose testing, and the majority of personal blood glucose meters are based on disposable (screen-printed) enzyme electrode test strips, which are mass produced by the thick film (screen-printing) microfabrication technology. In the counter and an additional “baseline” working electrode, various membranes (mesh) are incorporated into the test strips along with surfactants, to provide a uniform sample coverage. Such devices offer considerable promise for obtaining the desired clinical information in a simpler, user-friendly, faster, and cheaper manner compared to traditional assays. Continuous ex-vivo monitoring of blood glucose was proposed in 1974 and the majority of glucose sensors used for in-vivo applications are based on the GOx-catalyzed oxidation of glucose by oxygen. The major factors that play a role in the development of clinically accurate in-vivo glucose sensors include issues related to biocompatibility, miniaturization, long-term stability of the enzyme and transducer, oxygen deficit, short stabilization times, in-vivo calibration, baseline drift, safety, and convenience.

Electrochemical Glucose Biosensors

3.6.1. Polishing and Cleaning 2663 3.6.2. Vacuum and Heat Treatments 2664 3.6.3. Carbon Electrode Activation 2665 3.7. Summary and Generalizations 2666 4. Advanced Carbon Electrode Materials 2666 4.1. Microfabricated Carbon Thin Films 2666 4.2. Boron-Doped Diamond for Electrochemistry 2668 4.3. Fibers and Nanotubes 2669 4.4. Carbon Composite Electrodes 2674 5. Carbon Surface Modification 2675 5.1. Diazonium Ion Reduction 2675 5.2. Thermal and Photochemical Modifications 2679 5.3. Amine and Carboxylate Oxidation 2680 5.4. Modification by “Click” Chemistry 2681 6. Synopsis and Outlook 2681 7. Acknowledgments 2682 8. References 2682

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Advanced carbon electrode materials for molecular electrochemistry.

This review addresses recent advances in carbon-nanotubes (CNT) based electrochemical biosensors. The unique chemical and physical properties of CNT have paved the way to new and improved sensing devices, in general, and electrochemical biosensors, in particular. CNT-based electrochemical transducers offer substantial improvements in the performance of amperometric enzyme electrodes, immunosensors and nucleic-acid sensing devices. The greatly enhanced electrochemical reactivity of hydrogen peroxide and NADH at CNT-modified electrodes makes these nanomaterials extremely attractive for numerous oxidase- and dehydrogenase-based amperometric biosensors. Aligned CNT “forests” can act as molecular wires to allow efficient electron transfer between the underlying electrode and the redox centers of enzymes. Bioaffinity devices utilizing enzyme tags can greatly benefit from the enhanced response of the biocatalytic-reaction product at the CNT transducer and from CNT amplification platforms carrying multiple tags. Common designs of CNT-based biosensors are discussed, along with practical examples of such devices. The successful realization of CNT-based biosensors requires proper control of their chemical and physical properties, as well as their functionalization and surface immobilization.

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Carbon‐Nanotube Based Electrochemical Biosensors: A Review

Since their discovery, carbon nanotubes have attracted the attention of many a scientist around the world. This extraordinary interest stems from their outstanding structural, mechanical, and electronic properties. In fact, apart from being the best and most easily available one-dimensional (1D) model system, carbon nanotubes show strong application potential in electronics, scanning probe microscopy, chemical and biological sensing, reinforced composite materials, and in many more areas. While some of the proposed applications remain still a far-off dream, others are close to technical realization. Recent advances in the development of reliable methods for the chemical functionalization of the nanotubes provide an additional impetus towards extending the scope of their application spectrum. In particular, covalent modification schemes allow persistent alteration of the electronic properties of the tubes, as well as to chemically tailor their surface properties, whereby new functions can be implemented that cannot otherwise be acquired by pristine nanotubes.

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Chemically functionalized carbon nanotubes.

The remarkable electrocatalytic properties and small size of carbon nanotubes make them ideal for achieving direct electron transfer to proteins, important in understanding their redox properties and in the development of biosensors. Here, we report shortened SWNTs can be aligned normal to an electrode by self-assembly and act as molecular wires to allow electrical communication between the underlying electrode and redox proteins covalently attached to the ends of the SWNTs, in this case, microperoxidase MP-11. The efficiency of the electron transfer through the SWNTs is demonstrated by electrodes modified with tubes cut to different lengths having the same electron-transfer rate constant.

Protein electrochemistry using aligned carbon nanotube arrays.

The modification of an interface on a molecular level with more than one molecular ‘building block' is essentially an example of the ‘bottom–up' fabrication principle of nanotechnology. The fabrication of such integrated molecular systems in electrochemistry has seen rapid progress in recent years via the development of sensing interfaces fabricated using self-assembled monolayers (SAMs). This review outlines recent advances and applications of self-assembled monolayers for modifying electrodes with an emphasis on the development of integrated molecular systems. First, some basic issues regarding fabricating integrated molecular systems, such as the role of the surface topography of the electrode and patterning surfaces, are discussed. Subsequently an overview of recent developments in pH, inorganic and bio sensing involving the use of SAMs is given. Finally emerging trends in using molecular building blocks in the fabrication of integrated molecular systems, such as nanotubes, dendrimers and nanoparticles, are reviewed.

Self-Assembled Monolayers into the 21st Century: Recent Advances and Applications

Hybridization-induced physical changes of DNA are exploited in the development of DNA switchable surfaces for electrochemical biosensing purposes. Two types of biosensing concepts are explored, both based on the same basic switchable surface. The interface is designed so that the end-tethered DNA is able to switch from a flexible state to a rigid one upon hybridization. The first biosensing concept described is a label-free system that uses air oxidation of the interface, followed by the change in accessibility of the surface upon hybridization to detect complementary target DNA. The second is a ferrocene-labeled system exploiting the change in DNA flexibility alone. Atomic force microscopy studies of the DNA switching surface are described.

DNA Biosensor Concepts Based on a Change in the DNA Persistence Length upon Hybridization

The ion gating effect: using a change in flexibility to allow label free electrochemical detection of DNA hybridisation

An electrochemical DNA hybridization biosensor which exploits long-range electron transfer through double-stranded DNA (ds-DNA) to a redox intercalator is described. The DNA recognition interface consisted of a mixed self-assembled monolayer of synthetic thiolated single-stranded DNA (ss-DNA) and 6-mercapto-1-hexanol (MCH). The target DNA detection is performed electrochemically through cyclic and Osteryoung square wave voltammetry, using anthraquinone derivatives as the intercalators. This biosensor has the ability to differentiate complementary target ss-DNA from non-complementary target, and most importantly, it is able to detect single-base mismatch target ss-DNA through diminution in voltammetric current. The viability of this biosensor has also been investigated through selectivity studies in the presence of interferences and the generality of the detection scheme.

Freya J. Mearns

Papers

Protein electrochemistry using aligned carbon nanotube arrays.

Self-Assembled Monolayers into the 21st Century: Recent Advances and Applications

DNA Biosensor Concepts Based on a Change in the DNA Persistence Length upon Hybridization

The ion gating effect: using a change in flexibility to allow label free electrochemical detection of DNA hybridisation

Further development of an electrochemical DNA hybridization biosensor based on long-range electron transfer