1. Academic Validation
  2. An ultrasensitive electrochemical immunosensor for procalcitonin detection based on the gold nanoparticles-enhanced tyramide signal amplification strategy

An ultrasensitive electrochemical immunosensor for procalcitonin detection based on the gold nanoparticles-enhanced tyramide signal amplification strategy

  • Biosens Bioelectron. 2019 Feb 1:126:543-550. doi: 10.1016/j.bios.2018.10.048.
Pei Liu 1 Chao Li 2 Ruixuan Zhang 1 Qing Tang 1 Jia Wei 3 Yan Lu 1 Pingping Shen 4
Affiliations

Affiliations

  • 1 State Key Laboratory of Pharmaceutical Biotechnology and The Comprehensive Cancer Center, Nanjing Drum Tower Hospital, MOE Key Laboratory of Model Animal for Disease Study, School of Life Sciences, Nanjing University, Nanjing 210046, PR China.
  • 2 State Key Laboratory of Pharmaceutical Biotechnology and Collaborative Innovation Center of Chemistry for Life Sciences, School of Life Sciences, Nanjing University, Nanjing 210046, PR China.
  • 3 The Comprehensive Cancer Center, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing 210008, PR China.
  • 4 State Key Laboratory of Pharmaceutical Biotechnology and The Comprehensive Cancer Center, Nanjing Drum Tower Hospital, MOE Key Laboratory of Model Animal for Disease Study, School of Life Sciences, Nanjing University, Nanjing 210046, PR China. Electronic address: ppshen@nju.edu.cn.
Abstract

In this study, we established an ultrasensitive electrochemical immunosensor based on the gold nanoparticles-enhanced tyramide signal amplification (AuNPs-TSA) for the detection of procalcitonin (PCT, for discriminating Bacterial infections from nonbacterial infections). Firstly, a facilely prepared, well-conducting reduced graphene oxide nanosheets/GNP (rGO-AuNPs) nanocomposite was synthesized and immobilized on the electrode surface to absorb more capture antibodies (Ab1). Next another nanocomposite, acting as a signal tool, was modified with detection antibody (Ab2) and horseradish peroxidase (HRP), and then backfilled by bovine serum albumin (BSA). Because a single AuNP is able to load multiple HRPs and BSAs, a number of tyramine labeled biotins (T-B) could be deposited on the proteins adhering to the surface of AuNPs. Moreover, the high affinity between streptavidin (SA) and biotins significantly increases the loading of streptavidin labeled horseradish peroxidase (SA-HRP). The amplification system which was based on the two nanocomposites mentioned above, effectively amplified the electric current signals. This immunosensor exhibits a wide dynamic detection range from 0.05 ng mL-1 to 100 ng mL-1 and with an ultralow detection limit of 0.1 pg mL-1. We have successfully utilized this immunosensor to quantify the concentration of PCT in human serum samples, and the results suggest its potential use in clinical application.

Keywords

Antibiotic resistance; AuNPs; Immunosensor; Procalcitonin; Tyramide signal amplification.

Figures
Products