Abstract

In this study, carboxyl group functionalized-CdSe/ZnS quantum dots (QDs) and aminofluorescein (AF)-encapsulated polymer particles were synthesized and immobilized to a sol–gel mixture of glycidoxypropyl trimethoxysilane (GPTMS) and aminopropyl trimethoxysilane (APTMS) for the fabrication of a hydrogen peroxide-sensing membrane. CdSe/ZnS QDs were used for the redox reaction of hydrogen peroxide (H2O2) via a reductive pathway by transferring electrons to the acceptor that led to fluorescence quenching of QDs, while AF was used as a reference dye. Herein, the ratiometric fluorescence intensity of CdSe/ZnS QDs and AF was proportional to the concentration of hydrogen peroxide. The fluorescence membrane (i.e., QD–AF membrane) could detect hydrogen peroxide in linear detection ranges from 0.1 to 1.0 mM with a detection limit (LOD) of 0.016 mM and from 1.0 to 10 mM with an LOD of 0.058 mM. The sensitivity of the QD–AF membrane was increased by immobilizing horseradish peroxidase (HRP) over the surface of the QD–AF membrane (i.e., HRP–QD–AF membrane). The HRP–QD–AF membrane had an LOD of 0.011 mM for 0.1–1 mM H2O2 and an LOD of 0.068 mM for 1–10 mM H2O2. It showed higher sensitivity than the QD–AF membrane only, although both membranes had good selectivity. The HRP–QD–AF membrane could be applied to determine the concentration of hydrogen peroxide in wastewater, while the QD–AF membrane could be employed for the detection of α-ketobutyrate.

Highlights

  • Hydrogen peroxide (H2 O2 ) is usually one of the final products in many biological processes after biological substrates react with oxygen through the catalysis of some oxidases [1]

  • The horseradish peroxidase (HRP)–quantum dots (QDs)–AF membrane could be applied to determine the concentration of hydrogen peroxide in wastewater, while the quantum dot/aminofluorescein (QD–AF) membrane could be employed for the detection of α-ketobutyrate

  • After ligand exchange with carboxyl groups (MPA) on the surface of the synthesized CdSe/ZnS QDs, their fluorescence emission wavelength did not change significantly

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Summary

Introduction

Hydrogen peroxide (H2 O2 ) is usually one of the final products in many biological processes after biological substrates react with oxygen through the catalysis of some oxidases [1]. H2 O2 acts as a reactive oxygen species when it is excessively present above the tolerance threshold of biological organisms. The detection of H2 O2 and its control in each field are needed for safe human life. Among numerous analytical methods published for the detection of H2 O2 , fluorescence methods are the most preferred ones due to their high sensitivity and selectivity [1,10]. Many fluorescence probes showed strong affinity to react with

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