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The Use of a β-lactamase-based Conductimetric Biosensor Assay to Detect Biomolecular Interactions
Published on: February 1, 2018
A modular β-lactamase-based thermistor biosensor platform for rapid plasma monitoring of major β-lactam antibiotic
Qinglai Meng1, Youfan Wang1, Yingying Zou2
1Institute of Biomedical Sciences, The Key Laboratory of Chemical Biology and Molecular Engineering of National Ministry of Education, Shanxi University, Taiyuan, 030006, China.
Abstract:
Biosensors represent a promising approach for rapid therapeutic drug monitoring (TDM) of β-lactam antibiotics. However, no single biosensor strategy has yet been established to cover all four major β-lactam classes: penicillins, cephalosporins, carbapenems, and monobactams. Recently, an enzyme thermistor biosensor using New Delhi metallo-β-lactamase-1 (NDM-1) as the biorecognition element enabled the detection of penicillins, cephalosporins, and carbapenems in spiked plasma and supported accurate pharmacokinetic profiling of cefuroxime in treated patients. Here, we developed a CTX-M-14-coupled enzyme thermistor biosensor and compared its performance with that of the NDM-1 biosensor for detecting two penicillins, four extended-spectrum oxyimino-cephalosporins, one carbapenem, and one monobactam. Both β-lactamase-coupled biosensors achieved rapid response times of approximately 5 min. Across a plasma concentration range of 6.25-200 mg/L, the CTX-M-14-coupled biosensor quantified all tested penicillins, oxyimino-cephalosporins, the carbapenem, and the monobactam. In contrast, the NDM-1-coupled biosensor quantified penicillins, oxyimino-cephalosporins, and carbapenems, but not the monobactam. Although CTX-M-14 generally produced lower response signals than NDM-1 for most oxyimino-cephalosporins and the carbapenem, matrix effects for penicillins, oxyimino-cephalosporins and the monobactam were comparable between the two biosensors, with a significant difference observed only for the carbapenem. Plasma cefotaxime concentrations measured by the CTX-M-14-coupled biosensor in four treated patients closely matched UPLC-MS/MS results. Collectively, these findings support the CTX-M-14-coupled thermistor biosensor as a rapid and accurate approach for quantifying penicillins, oxyimino-cephalosporins, carbapenems, and monobactams in plasma, and highlight enzyme thermistor biosensing as a flexible platform for TDM of full-spectrum β-lactam antibiotics.
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