4.7 Article

Photoreduced Ag+ surrounding single poly(4-cyanostyrene) nanoparticles for undifferentiated SERS sensing and killing of bacteria

Journal

TALANTA
Volume 245, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.talanta.2022.123450

Keywords

SERS; Bacteria; Undifferentiated sensing and killing; Silver ions; Photoreduction

Funding

  1. National Natural Science Foundation of China [22074109, 21874102, 21775114]
  2. China Postdoctoral Science Foundation [2021M702506]

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A direct photoreduction method was proposed for the rapid detection and killing of bacterial pathogens. The method synthesized SERS tags by integrating poly(4-cyanostyrene) nanoparticles and silver ions, and used 4-mercaptophenylboronic acid as a bridge and recognition molecule. The strategy achieved quick and sensitive bacteria counting and killing with high accuracy.
Developing a rapid, low cost and sensitive sensing strategy for undifferentiated detection and fast killing of bacterial pathogens are critical to alleviating bacteria infections. Here, we propose a direct photoreduction method to synthesize the SERS tag by integrating poly(4-cyanostyrene) nanoparticles (NPs) and silver ions, which are applied as bio-sensing system for bacteria sensing and fast killing. Under a focused laser spot, silver ions on the surface of the poly(4-cyanostyrene) NPs could be photoreduced into Ag NPs, thereby causing the Raman signal amplification of poly(4-cyanostyrene) NPs up to 40 times, and there is a good linear correlation between the Raman intensity of poly(4-cyanostyrene) NPs and different concentrations of Ag+. Moreover, 4-mercaptophenylboronic acid, performing the same recognition function for both the Gram-positive and Gram-negative bacteria, is used as bridge between the bacteria and Ag+ by the inherent chemical bonding. Based on further constructed bio-sensing system, we achieved the quick count and killing of both Gram-positive bacteria, e.g., Staphylococcus aureus (S. aureus), and Gram-negative bacteria, e.g., Escherichia coli (E. coli). Notably, the sensing strategy can detect at least -100 cells of E. coli, -10 cells of S. aureus and -10 cells of their mixture in less than 40 min. The detection accuracy for actual samples can also reach over 80% and the bacteria were entirely killed by Ag(+ )after the detection, avoiding bacterial contamination in the environment. This novel method is anticipated to perform as a simple yet effective tool for fast and sensitive bacteria counting and killing.

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