研究目的
Development of a selective and sensitive sensor for the determination of trace amounts of lidocaine in biological samples using quantum dots and molecularly imprinted polymers.
研究成果
The glass slide@QDs@MIP sensor demonstrated high selectivity and sensitivity for lidocaine detection in biological samples, with advantages including photostability and rapid detection. The sensor's performance suggests its potential for practical applications in monitoring lidocaine levels in complex matrices.
研究不足
The study did not explore the sensor's performance in the presence of a wide range of potential interferents beyond structural analogs of lidocaine. The long-term stability beyond one month was not assessed.
1:Experimental Design and Method Selection
The study involved the fabrication of a glass slide@QDs@MIP sensor for lidocaine detection. The methodology included covalent attachment of CdSeS/ZnS quantum dots to a glass slide followed by embedding a molecularly imprinted polymer layer using lidocaine as the template.
2:Sample Selection and Data Sources
Biological samples (urine and plasma) were used for practical application. Samples were prepared by centrifugation and dilution with deionized water.
3:List of Experimental Equipment and Materials
Spectrofluorophotometer RF-6000, Mira 3 TESCAN scanning electron microscope, Universal 320R refrigerated centrifuge, pH meter, microscope glass slides.
4:Experimental Procedures and Operational Workflow
The glass slide was modified with amino functional groups, then QDs were attached. A molecularly imprinted polymer layer was synthesized around the QDs using lidocaine as the template. The sensor was used to extract lidocaine from samples, followed by fluorescence measurement.
5:Data Analysis Methods
Fluorescence quenching was measured using a spectrofluorophotometer. Data analysis involved the Stern-Volmer equation for quantifying lidocaine concentration.
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