Simple and fast colorimetric detection of lipopolysaccharide based on aptamer and SYBR Green I mediated aggregation of gold nanoparticles

Int J Biol Macromol. 2022 Dec 31;223(Pt A):231-239. doi: 10.1016/j.ijbiomac.2022.10.276. Epub 2022 Nov 5.

Abstract

Lipopolysaccharide (LPS) poses a considerable threat to food safety and human health. A colorimetric assay for LPS detection based on LPS binding aptamer (LBA) and SYBR Green I (SG) mediated aggregation of gold nanoparticles (AuNPs) was established. In the absence of LPS, the LBA was absorbed onto the AuNPs surface which prevented SG-induced aggregation of AuNPs, and the sensing system exhibited red color. When LPS was added, it interacted with the LBA, forming a complex. At higher LPS concentration, many LBAs were exhausted resulting in SG-induced aggregation of AuNPs, and color change from red to blue. The range of colorimetric detection of LPS was linear in 0-12 EU/mL, with a limit of detection of 0.1698 EU/mL. Spiked LPS in real samples and interfering substances were also identified. This assay ingeniously using the fluorescent dye SG as an effective trigger of AuNPs aggregation, is rapid and facile than most of those earlier reported LBA-based LPS assays, and there is potential to be modified to construct assays for other targets.

Keywords: Aptamer; Colorimetric detection; Endotoxin; Gold nanoparticle; Lipopolysaccharide; SYBR Green.

MeSH terms

  • Aptamers, Nucleotide* / chemistry
  • Biosensing Techniques* / methods
  • Colorimetry / methods
  • Gold / chemistry
  • Humans
  • Lipopolysaccharides
  • Metal Nanoparticles* / chemistry

Substances

  • Gold
  • SYBR Green I
  • Aptamers, Nucleotide
  • Lipopolysaccharides