A rapid aptamer-based fluorescence assay for the detection of lipopolysaccharides using SYBR Green I

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Date

2021

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John Wiley and Sons Ltd

Abstract

Lipopolysaccharides (endotoxins), found on Gram-negative bacteria, can trigger a severe immune response in humans leading to septic shock and in extreme cases, even death. Therefore, the detection and neutralization of lipopolysaccharides (LPS) is of utmost importance in the pharmaceutical and medical industries. The United States Food and Drug Administration (US FDA) recommended detection method for LPS, the Limulus amebocyte lysate (LAL) assay, is expensive, time consuming, complex, and is prone to interference from proteases. As an alternative, this paper proposes a rapid, label-free fluorescence-based assay using LPS-specific aptamers and the SYBR Green DNA stain. The proposed method has a detection limit of 0.1 ng/ml, which is sufficient to detect the permissible levels of LPS in many pharmaceutical drugs and medical products. The fluorescence signal was found to be a linear function of the concentration of LPS in the range from 0.1 ng/ml to 105 ng/ml. © 2021 John Wiley & Sons Ltd.

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Keywords

Bacteria, Drug products, Polysaccharides, Aptamers, Aptasensors, Endotoxin, Fluorescence assay, Fluorescence detection, Gram-negative bacteria, Immune response, Lipopolysaccharides, SYBR Green, SYBR Green I, Fluorescence, benzothiazole derivative, diamine, endotoxin, lipopolysaccharide, oligonucleotide, quinoline derivative, bioassay, human, United States, Benzothiazoles, Biological Assay, Diamines, Endotoxins, Humans, Oligonucleotides, Quinolines

Citation

Luminescence, 2021, 36, 7, pp. 1632-1637

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