DNA Biosensor for the Detection of Hydrazines
- 1 July 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Analytical Chemistry
- Vol. 68 (13) , 2251-2254
- https://doi.org/10.1021/ac9600619
Abstract
A double-stranded (ds) DNA-coated carbon paste electrode is employed as a remarkably sensitive biosensor for the detection of hydrazine compounds. The sensor relies on monitoring changes in the intrinsic anodic response of the surface-confined DNA resulting from its interaction with hydrazine compounds and requires no label or indicator. Short reaction times (1−10 min) are sufficient for monitoring part-per-billion levels of different hydrazines. Applicability to untreated natural water samples is illustrated. The response mechanism is discussed, along with prospects of using DNA biosensors for quantitaing other important molecules and elucidating DNA interactions and damage.Keywords
This publication has 11 references indexed in Scilit:
- Electrochecmical biosensors for DNA sequence detectionElectroanalysis, 1996
- From polarography of DNA to microanalysis with nucleic acid‐modified electrodesElectroanalysis, 1996
- Trace Measurements of RNA by Potentiometric Stripping Analysis at Carbon Paste ElectrodesAnalytical Chemistry, 1995
- Hydrazine Detection Using a Tyrosinase-Based Inhibition BiosensorAnalytical Chemistry, 1995
- Hydralazine and Other Hydrazine Derivatives and the Formation of DNA AdductsToxicology and Applied Pharmacology, 1994
- Application of Photochemical Reaction in Electrochemical Detection of DNA IntercalationAnalytical Chemistry, 1994
- Fiber optic biosensor for fluorimetric detection of DNA hybridizationAnalytica Chimica Acta, 1994
- Hydrazine-Mediated DNA Damage: Role of Hemoprotein, Electron Transport, and Organic Free RadicalsToxicology and Applied Pharmacology, 1994
- Adsorptive transfer stripping voltammetry: Determination of nanogram quantities of DNA immobilized at the electrode surfaceAnalytical Biochemistry, 1988
- Consequences of light beam misalignment in background corrected atomic absorption spectrometersAnalytical Chemistry, 1984