Robotic voltammetry with carbon nanotube-based sensors: a superb blend for convenient high-quality antimicrobial trace analysis

Somjai Theanponkrang,1,2 Wipa Suginta,2,3 Helge Weingart,4 Mathias Winterhalter,4 Albert Schulte1,2 1School of Chemistry, 2Biochemistry–Electrochemistry Research Unit, Institute of Science, 3School of Biochemistry, Suranaree University of Technology, Nakhon Ratchasima, Thailand; 4Life Sci...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Theanponkrang S, Suginta W, Weingart H, Winterhalter M, Schulte A
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://doaj.org/article/b13435cba2ea49358947a203331c9ecd
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
Descripción
Sumario:Somjai Theanponkrang,1,2 Wipa Suginta,2,3 Helge Weingart,4 Mathias Winterhalter,4 Albert Schulte1,2 1School of Chemistry, 2Biochemistry–Electrochemistry Research Unit, Institute of Science, 3School of Biochemistry, Suranaree University of Technology, Nakhon Ratchasima, Thailand; 4Life Sciences, School of Engineering and Science, Jacobs University Bremen, Bremen, Germany Abstract: A new automated pharmacoanalytical technique for convenient quantification of redox-active antibiotics has been established by combining the benefits of a carbon nanotube (CNT) sensor modification with electrocatalytic activity for analyte detection with the merits of a robotic electrochemical device that is capable of sequential nonmanual sample measurements in 24-well microtiter plates. Norfloxacin (NFX) and ciprofloxacin (CFX), two standard fluoroquinolone antibiotics, were used in automated calibration measurements by differential pulse voltammetry (DPV) and accomplished were linear ranges of 1–10 µM and 2–100 µM for NFX and CFX, respectively. The lowest detectable levels were estimated to be 0.3±0.1 µM (n=7) for NFX and 1.6±0.1 µM (n=7) for CFX. In standard solutions or tablet samples of known content, both analytes could be quantified with the robotic DPV microtiter plate assay, with recoveries within ±4% of 100%. And recoveries were as good when NFX was evaluated in human serum samples with added NFX. The use of simple instrumentation, convenience in execution, and high effectiveness in analyte quantitation suggest the merger between automated microtiter plate voltammetry and CNT-supported electrochemical drug detection as a novel methodology for antibiotic testing in pharmaceutical and clinical research and quality control laboratories. Keywords: antibiotics, electroanalysis, automation, microtiter plates, pharmaceutical screening, pharmacoanalytics