Investigations on Bioanalytical Chemistry Part I. On Differential Pulse Voltammetry of Bilirubin
Wenrui Jin, Xin Zhao, Chen Ding, Funing Wang, Zuquan Gao
Abstract
Wenrui Jin, Xin Zhao, Chen Ding, Funing Wang, Zuquan Gao
Abstract
The electrochemical behaviour of the bilirubin in many kinds of supporting electrolytes on a glassy carbon electrode (GCE) and a hanging mercury drop electrode (HMDE) was investigated by means of anodic or cathodic differential pulse voltammetry. The influences of different methods of pre-treatment of the glassy carbon electrode was also discussed. In Na2B4.O7-KH2PO4 buffer solution, the linear range was 2×10−9-1×10−9 mol/l and the detection limit was 3.3×10−9 mol/l by anodic differential pulse voltammetry at GCE. A linear relationship holds between the peak current and the concentration of bilirubin in a concentration range of 1×10−9-4×10−7 mol/l with good precision and accuracy, and the limit of detection was 2×10−10 mol/l, when cathodic differential pulse adsorption voltammetry at HMDE was used.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The electrochemical behaviour of the bilirubin in many kinds of supporting electrolytes on a glassy carbon electrode (GCE) and a hanging mercury drop electrode (HMDE) was investigated by means of anodic or cathodic differential pulse voltammetry. The influences of different methods of pre-treatment of the glassy carbon electrode was also discussed. In Na2B4.O7-KH2PO4 buffer solution, the linear range was 2×10−9-1×10−9 mol/l and the detection limit was 3.3×10−9 mol/l by anodic differential pulse voltammetry at GCE. A linear relationship holds between the peak current and the concentration of bilirubin in a concentration range of 1×10−9-4×10−7 mol/l with good precision and accuracy, and the limit of detection was 2×10−10 mol/l, when cathodic differential pulse adsorption voltammetry at HMDE was used.
Key concepts: Chemistry, Hanging mercury drop electrode, Differential pulse voltammetry, Detection limit, Voltammetry, Supporting electrolyte, Analytical Chemistry (journal), Electrochemistry