4.7 Article

Elimination of background color interference by immobilizing Prussian blue on carbon cloth: A monolithic peroxidase mimic for on-demand photometric sensing

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 256, 期 -, 页码 151-159

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2017.10.072

关键词

Prussian blue; Nanozyme; Colorimetric detection; H2O2; Uric acid

资金

  1. National Natural Science Foundation of China [21605061, 31601549]
  2. Natural Science Foundation of Jiangsu Province [BK20160489]
  3. Natural Science Fund for Colleges and Universities in Jiangsu Province [16KJB150009]
  4. Postdoctoral Fund of China [2016M600365]
  5. Postdoctoral Fund of Jiangsu Province [1601015B]
  6. Shanghai Key Laboratory of Functional Materials Chemistry [SKLFMC201601]
  7. Jiangsu University [15JDG143]
  8. Youth Talent Cultivation Plan of Jiangsu University
  9. State Key Laboratory of Bioreactor Engineering

向作者/读者索取更多资源

Prussian blue (PB) is widely used as an artificial peroxidase for electrochemical biosensors, yet it is rarely utilized in photometric detection because of its intrinsic color interference. Herein, we proposed a new strategy, growing PB on common carbon cloth (CC), to obtain a monolithic peroxidase mimic with no background interference for colorimetric detection. Through a one-pot two-step electrodeposition procedure, a robust PB film composed of compactly assembled cubes was coated on CC surface. Since the active PB is immobilized on a bulk substrate (not like previous nanozymes that were dispersed in solution), the color interference from PB itself is efficiently avoided. In addition, the obtained monolithic nanozyme can be put into and taken out from reaction systems expediently and promptly with just a tiny pair of tweezers, which makes it possible for on-demand detection. As demonstrated, the PB-based nanozyme exhibited excellent peroxidase-like activity and could trigger the color reaction of 3,3'5,5'-tetramethylbenzidine in the presence of H2O2, leading to a detection limit of as low as 1.7 mu M for H2O2 sensing. A uric acid (UA) colorimetric assay was further established by incorporating the PB/CC peroxidase mimic with natural uricase, providing a linear absorbance response in the analyte concentration scope of 10-700 mu M. Reliable analysis of UA in human serum and urine verified the practicability of the fabricated assay. (C) 2017 Elsevier B.V. All rights reserved.

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