4.7 Article

Highly sensitive and label-free detection of catalase by a H2O2-responsive liquid crystal sensing platform

Journal

SENSORS AND ACTUATORS B-CHEMICAL
Volume 344, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2021.130279

Keywords

Catalase; Hydrogen peroxide; Liquid crystal; Detection; Surfactant; Interface

Funding

  1. National Natural Science Foundation of China [21972074, 81801790]
  2. Taishan Scholars Program [tsqn201812088]

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A H2O2-responsive liquid crystal sensing platform was developed and utilized for detecting catalase in human serum, showing high sensitivity and label-free detection capabilities.
Abnormal levels of catalase are implicated in multiple clinical diseases, so it is of great importance to monitor the levels of catalase in real samples. In this report, a H2O2-responsive liquid crystal (LC) sensing platform was developed and applied to the detection of catalase in human serum for the first time. The platform was constructed by doping LCs with a synthesized surfactant, namely N,N-dimethyl-N-(4-(4,4,5,5-tetramethyl-1,3,2dioxaborolan-2-yl)benzyl)tetradecan-1-aminium bromide (PBEC14A), which can be decomposed by H2O2. Selfassembled monolayers formed at the aqueous/LC interface when immersing the surfactant-doped LCs into an aqueous solution. Accordingly, the LCs displayed a dark image that indicates a perpendicular state of the LCs at the interface. However, when H2O2 was present in the aqueous solution, the optical image of the LCs became bright that represents a planar state of the LCs at the interface. It is caused by disruption of the surfactant monolayers due to decomposition of PBEC14A by H2O2. Interestingly, it was found that the LCs still displayed the dark image when the pre-incubated mixture of catalase and H2O2 was transferred onto the LC sensing platform due to enzymatic hydrolysis of H2O2 by catalase. The detection limit of catalase reached as low as 5.5 mU/mL. In addition, it also shows excellent performance for the detection of catalase in human serum. As a simple and convenient method, it shows high promise in the highly sensitive and label-free detection of catalase in practical applications.

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