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1.
Methods Mol Biol ; 300: 191-23, 2005.
Article in English | MEDLINE | ID: mdl-15657485

ABSTRACT

This chapter reviews the recent development in biological sensing using nanotechnologies based on carbon nanotubes and various nanowires. These 1D materials have shown unique properties that are efficient in interacting with biomolecules of similar dimensions, i.e., on a nanometer scale. Various aspects including synthesis, materials properties, device fabrication, biofunctionalization, and biological sensing applications of such materials are reviewed. The potential of such integrated nanobiosensors in providing ultrahigh sensitivity, fast response, and high-degree multiplex detection, yet with minimum sample requirements is demonstrated. This chapter is intended to provide comprehensive updated information for people from a variety of backgrounds but with common interests in the fast-moving interdisciplinary field of nanobiotechnology.


Subject(s)
Biosensing Techniques/instrumentation , Nanotubes, Carbon , Biosensing Techniques/methods , DNA/ultrastructure , Microscopy, Electron, Scanning , Microscopy, Scanning Probe , Nanotubes, Carbon/ultrastructure , Palladium , Peptides/analysis
2.
Biosens Bioelectron ; 19(1): 43-9, 2003 Oct 30.
Article in English | MEDLINE | ID: mdl-14558997

ABSTRACT

In this paper, a mediatorless amperometric glucose biosensor based on direct covalent immobilisation of monomolecular layer of glucose oxidase (GOx) on a semiconducting indium-tin oxide (ITO) is demonstrated. The abundance of surface hydroxyl functional group of ITO allows it to be used as a suitable platform for direct covalent immobilisation of the enzyme for sensor architecture. The anodic current corresponding to electrochemical oxidation of the enzymatic product, hydrogen peroxide, at a sputtered Pt electrode at 0.500 V (vs. SCE) was obtained as the sensor signal. It was found that the biosensor based on the direct immobilisation scheme shows a fast biosensor response, minimum interference from other common metabolic species and ease of biosensor miniaturisation. A linear range of 0-10 mM of glucose was demonstrated, which exhibits a high sensitivity as far as performance per immobilised GOx molecule is concerned. A detection limit as low as 0.05 mM and long-term stability were observed. Even more important, the biosensor design allows fabrication through a dry process. These characteristics make it possible to achieve mass production of biosensor compatible with the current electronic integrated circuit manufacturing technologies.


Subject(s)
Biosensing Techniques/instrumentation , Electrochemistry/instrumentation , Glucose Oxidase/chemistry , Glucose/analysis , Glucose/chemistry , Microchemistry/instrumentation , Tin Compounds/chemistry , Adsorption , Biosensing Techniques/methods , Blood Glucose/analysis , Coated Materials, Biocompatible/chemical synthesis , Coated Materials, Biocompatible/chemistry , Electrochemistry/methods , Electrodes , Enzymes, Immobilized/chemistry , Equipment Design , Equipment Failure Analysis , Microchemistry/methods , Quality Control , Reproducibility of Results , Sensitivity and Specificity
3.
Nanotechnology ; 14(12): 1239-45, 2003 Dec.
Article in English | MEDLINE | ID: mdl-21444977

ABSTRACT

We report the detection of DNA PCR amplicons using an ultrasensitive label-free electronic technique based on multiwalled carbon nanotube (MWNT) nanoelectrode arrays embedded in an SiO(2) matrix. Specific PCR amplicons are reliably detected using electrochemical (EC) methods through allele-specific oligonucleotide hybridization. The inherent guanine bases in the DNA amplicon target of [Formula: see text] bases serve as signal moieties with the aid of Ru(bpy)(3)(2+) mediators, providing an amplified anodic current associated with the oxidation of guanine groups at the nanoelectrode surface. The reduced size and density of the nanoelectrode array provided by MWNTs dramatically improves the sensitivity of EC detection. In addition, the abundant guanine bases in target DNA produce a large signal. Less than [Formula: see text] target amplicons can be detected on a microspot, approaching the sensitivity limit of conventional laser-based fluorescence techniques. This method also eliminates the labelling requirement and makes the measurements much simpler. This platform can be employed for developing highly automated electronic chips with multiplex nanoelectrode arrays for quick DNA analysis.

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