4.7 Article

N,N-Dimethyl-4,4′-azodianiline functionalized magnetic nanoparticles for enhanced sensitivity of nucleic acid amplification tests

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 332, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2021.129461

关键词

Azobenzene; Bacterial pathogen sample preparation; Hydrophobic ligand; Urinary tract infection; Bacterial pathogen enrichment

资金

  1. Basic Science Research Program through the National Research Foundation of Korea - Ministry of Education [2019R1I1A3A01063051]
  2. Chungnam National University
  3. National Research Foundation of Korea [2019R1I1A3A01063051] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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A novel molecular diagnostic method was developed for highly efficient detection of gram-negative bacterial pathogens in challenging samples with low abundance and nucleic acid amplification inhibitory factors. The method utilized magnetic nanoparticles for bacteria enrichment and DNA extraction, resulting in improved DNA yield and quality for enhanced qPCR signal. Evaluation using various gram-negative bacteria showed successful detection and potential application for urinary tract infection diagnosis.
A facile molecular diagnostic method was devised for highly efficient detection of gram-negative bacterial pathogens with low abundance in umlogical samples, which contain various inhibitory factors of nucleic acid amplification. We developed a magnetic nanoparticle with N,N-Dimethyl-4,4'-azodianiline for bacterial pathogen sample preparation combining nucleic acid amplification test for bacterial pathogen detection and identification. We employed N,N-Dimethyl-4,4'-azodianiline functionalized nanoparticles to enable a dual strategy integrated within a single tube: (i) bacteria enrichment via the hydrophobic effect and (ii) DNA extraction and isolation via electrostatic interaction under pH control. It provided more yield and higher-quality DNA, resulting in a significant increase in fluorescent signal of quantitative PCR (qPCR). We evaluated our proposed method using gram-negative bacteria including Salmonella enterica serover Typhimurium (S. Typhimurium), Escherichia coli (E. coli), Klebsiella pneumonia (K. pneumonia) and Brucella ovis (B. ovis), found in human urine samples. Our proposed method resulted in a detection limit of five colony-forming units (CFU)/10 mL for S. Typhimurium and 10 CFLJ/10 mL for E. coli, and resulted in the detection of B. ovis and K. pneumonia. This novel method provides simple and sensitive detection of gram-negative bacteria species and can be used for diagnosis of urinary tract infections.

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