Microfluidic paper-based device for colorimetric determination of glucose based on a metal-organic framework acting as peroxidase mimetic

被引:0
|
作者
Inmaculada Ortiz-Gómez
Alfonso Salinas-Castillo
Amalia García García
José Antonio Álvarez-Bermejo
Ignacio de Orbe-Payá
Antonio Rodríguez-Diéguez
Luis Fermín Capitán-Vallvey
机构
[1] University of Granada,ECsens, Department of Analytical Chemistry
[2] University of Granada,Department of Inorganic Chemistry, Campus Fuentenueva, Faculty of Sciences
[3] University of Almeria,Department of Information Technology
来源
Microchimica Acta | 2018年 / 185卷
关键词
μPADs; Enzyme mimic; Photographic camera; Smartphone app; Colorimetric assay; Glucose monitoring; 3,3′,5,5′-Tetramethylbenzidine;
D O I
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学科分类号
摘要
This work presents a microfluidic paper-based analytical device (μPAD) for glucose determination using a supported metal-organic framework (MOF) acting as a peroxidase mimic. The catalytic action of glucose oxidase (GOx) on glucose causes the formation of H2O2, and the MOF causes the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) by H2O2 to form a blue-green product with an absorption peak at 650 nm in the detection zone. A digital camera and the iOS feature of a smartphone are used for the quantitation of glucose with the S coordinate of the HSV color space as the analytical parameter. Different factors such as the concentration of TMB, GOx and MOF, pH and buffer, sample volume, reaction time and reagent position in the μPAD were optimized. Under optimal conditions, the value for the S coordinate increases linearly up to 150 μmol·L−1 glucose concentrations, with a 2.5 μmol·L−1 detection limit. The μPAD remains stable for 21 days under conventional storage conditions. Such an enzyme mimetic-based assay to glucose determination using Fe-MIL-101 MOF implemented in a microfluidic paper-based device possesses advantages over enzyme-based assays in terms of costs, durability and stability compared to other existing glucose determination methods. The procedure was applied to the determination of glucose in (spiked) serum and urine.
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