A novel amperometric hydrogen peroxide biosensor based on the immobilization of hemoglobin on the 2,6-pyridinedicarboxylic acid (PDC) polymer, thionine and nano-Au was successfully fabricated. In this strategy, PDC polymer acted as the matrices to covalently immobilize the thionine, and then hemoglobin was successfully adsorbed on the nano-Au which was electro-deposited on to thionine modified electrode surface. The preparation process of modified electrode was characterized with electrochemical impedance spectroscopy and atomic force microscope. The analytical performance of proposed biosensor toward H(2)O(2) was investigated by cyclic voltammetry and chronoamperometry. The resulted biosensor exhibited fast amperometric response (within 6 s) to H(2)O(2), and linear range was from 9.1 microM to 5.0 mM with the detection limit of 2.6 microM (S/N = 3). The apparent Michaelis-Menten constant (K(M)(app)) was evaluated to be 3.2 mM. Furthermore, the resulted biosensor showed good stability and reproducibility.
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http://dx.doi.org/10.1007/s00449-008-0275-8 | DOI Listing |
Sensors (Basel)
January 2025
Laboratory of Sensors/Actuators and Energy Harvesting, National Institute for Research and Development in Electrical Engineering ICPE-CA, 030138 Bucharest, Romania.
The use of hydrogen as fuel presents many safety challenges due to its flammability and explosive nature, combined with its lack of color, taste, and odor. The purpose of this paper is to present an electrochemical sensor that can achieve rapid and accurate detection of hydrogen leakage. This paper presents both the component elements of the sensor, like sensing material, sensing element, and signal conditioning, as well as the electronic protection and signaling module of the critical concentrations of H.
View Article and Find Full Text PDFBiosens Bioelectron
December 2024
Centre for Biomedicine, Hull York Medical School, University of Hull, Hull HU6 7RX, United Kingdom. Electronic address:
Early detection of hepatitis C virus (HCV) infection is crucial for eliminating this silent killer, especially in resource-limited settings. HCV core antigen (HCVcAg) represents a promising alternative to the current "gold standard" HCV RNA assays as an active viremia biomarker. Herein, a highly sensitive electrochemical magneto-immunosensor for the HCVcAg was developed.
View Article and Find Full Text PDFBiosensors (Basel)
December 2024
Department of Cogno-Mechatronics Engineering, College of Nanoscience and Nanotechnology, Pusan National University, Busan 46241, Republic of Korea.
Enzyme-based portable amperometric biosensors are precise and low-cost medical devices used for rapid cancer biomarker screening. Sarcosine (Sar) is an ideal biomarker for prostate cancer (PCa). Because human serum and urine contain complex interfering substances that can directly oxidize at the electrode surface, rapid Sar screening biosensors are relatively challenging and have rarely been reported.
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November 2024
Department of Chemical Engineering, Ariel University, Kyriat-ha-Mada, Ariel 4070000, Israel.
We report the development of amperometric biosensors (ABSs) employing flavocytochrome (Fc) coupled with nanoparticles (NPs) of noble metals on graphite electrode (GE) surfaces. Each NPs/GE configuration was evaluated for its ability to decompose hydrogen peroxide (HO), mimicking peroxidase (PO) activity. The most effective nanoPO (nPO) was selected for developing ABSs targeting L-lactate.
View Article and Find Full Text PDFAdv Sci (Weinh)
December 2024
School of Petrochemical Technology, Lanzhou University of Technology, Lanzhou, Gansu, 730050, China.
Effective hydrogen evolution reaction (HER) under high current density and enhanced hydrogen oxidation reaction (HOR) over a wide potential range remain challenges for Ru-based electrocatalysts because its strong affinity to the adsorbed hydroxyl (OH) inhibits the supply of the adsorbed hydrogen (H). Herein, the coexisting Ru─O─Ti and Ru─Ti bonds are constructed by taking TiO crystal confined flat-Ru clusters (F-Ru@TiO) to cope with above-mentioned obstacles. The different electronegativity (χ = 1.
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