Literature DB >> 31098745

A new colorimetric assay for amylase based on starch-supported Cu/Au nanocluster peroxidase-like activity.

Zahra Dehghani1, Javad Mohammadnejad1, Morteza Hosseini2.   

Abstract

In this paper, we present a new colorimetric technique as a novel assay for the easy and direct detection of α-amylase activity. This detection system utilizes the interaction of α-amylase with starch that is supporting copper/gold (Cu/Au) nanoclusters. The Cu/Au nanoclusters are synthesized using starch as a stabilizing agent at room temperature. These nanoclusters show robust peroxidase-like activity and are able to catalyze the oxidation of TMB (3,3,5,5-tetramethylbenzidine) in the presence of hydrogen peroxide (H2O2), leading to the generation of a blue-colored solution. The α-amylase detection mechanism is based on the digestion of the starch by α-amylase, which results in nanocluster aggregation, leading to increased nanoparticle size and thus decreased peroxidase-like activity of the Cu/Au NCs. Experiments showed that the gradual addition of α-amylase causes the peroxidase activity to decrease step by step in a linear fashion. Using this method, colorimetric sensing of α-amylase was achieved with a detection limit (LOD) of 0.04 U/mL and a linear range of 0.1-10 U/mL. This method is significantly selective for α-amylase and could be affordably and conveniently applied to the detection of α-amylase in blood serum. Graphical Abstract.

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Keywords:  Copper/gold; Nanocluster; Peroxidase-like activity; α-Amylase

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Year:  2019        PMID: 31098745     DOI: 10.1007/s00216-019-01844-9

Source DB:  PubMed          Journal:  Anal Bioanal Chem        ISSN: 1618-2642            Impact factor:   4.142


  1 in total

1.  Detection of Escherichia coli O157:H7 Using Automated Immunomagnetic Separation and Enzyme-Based Colorimetric Assay.

Authors:  Ji Young Park; Kisang Park; Gyeongsik Ok; Hyun-Joo Chang; Tae Jung Park; Sung-Wook Choi; Min-Cheol Lim
Journal:  Sensors (Basel)       Date:  2020-03-04       Impact factor: 3.576

  1 in total

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