DNA Electrochemical Biosensors for In Situ Probing of Pharmaceutical Drug Oxidative DNA Damage

Deoxyribonucleic acid (DNA) electrochemical biosensors are devices that incorporate immobilized DNA as a molecular recognition element on the electrode surface, and enable probing in situ the oxidative DNA damage. A wide range of DNA electrochemical biosensor analytical and biotechnological applications in pharmacology are foreseen, due to their ability to determine in situ and in real-time the DNA interaction mechanisms with pharmaceutical drugs, as well as with their degradation products, redox reaction products, and metabolites, and due to their capacity to achieve quantitative electroanalytical evaluation of the drugs, with high sensitivity, short time of analysis, and low cost. This review presents the design and applications of label-free DNA electrochemical biosensors that use DNA direct electrochemical oxidation to detect oxidative DNA damage. The DNA electrochemical biosensor development, from the viewpoint of electrochemical and atomic force microscopy (AFM) characterization, and the bottom-up immobilization of DNA nanostructures at the electrode surface, are described. Applications of DNA electrochemical biosensors that enable the label-free detection of DNA interactions with pharmaceutical compounds, such as acridine derivatives, alkaloids, alkylating agents, alkylphosphocholines, antibiotics, antimetabolites, kinase inhibitors, immunomodulatory agents, metal complexes, nucleoside analogs, and phenolic compounds, which can be used in drug analysis and drug discovery, and may lead to future screening systems, are reviewed.

Ultrasensitive DNA electrochemical biosensor based on MnTBAP biomimetic catalyzed AGET ATRP signal amplification reaction

In this paper, an ultrasensitive, highly selective and green electrochemical biosensor for quantifying DNA sequences (aM DNA) based on a MnTBAP catalyst for AGET ATRP reaction is proposed.

Multi-walled carbon nanotubes/nano-Ag-TiO2 membrane DNA electrochemical biosensor

A highly sensitive DNA electrochemical biosensor was prepared based on multi-walled carbon nanotube/nano-Ag-TiO2 composite membrane. The Ag-TiO2 composite is mixed with a suitable amount of multi-walled carbon nanotubes (MWNT) dispersed in N,N-dimethylformamide to form a uniform and stable mixed solution, which is applied onto the surface of the bare carbon paste electrode. A MWNT/Ag-TiO2 modified carbon paste electrode was prepared. The large specific surface area and good electron transport properties of carbon nanotubes have a good synergistic effect on the good biocompatibility of Ag-TiO2 nanocomposites and excellent adsorption capacity of DNA, which significantly improves the immobilization and DNA hybridization of DNA probes. Detection sensitivity. The preparation of the sensing membrane and the immobilization and hybridization of DNA were characterized by cyclic voltammetry and electrochemical impedance spectroscopy. The exogenous glufosinate acetyltransferase gene fragment of transgenic plants was detected by electrochemical impedance spectroscopy. The linear range was 1. 0 × 10 - 11 ∼1. 0 × 10 - 6 mol / L. The detection limit was 3. 12 × 10 - 12 mol / L.

Construction of self-signal DNA electrochemical biosensor employing WS2 nanosheets combined with PIn6COOH

A self-signal DNA electrochemical biosensor was constructed employing WS2 nanosheets combined with PIn6COOH.