| Literature DB >> 25172133 |
Ming-Yan Zuo1, Li-Juan Chen1, Hao Jiang2, Lin Tan1, Zhao-Feng Luo3, Yan-Mei Wang1.
Abstract
Endotoxin, which is also known as lipopolysaccharide (LPS), is a marker for intruding gram-negative pathogens. It is essential to detect endotoxin quickly and sensitively in a complex milieu. A new flow cytometry (FCM)-based magnetic aptasensor assay that employs two endotoxin-binding aptamers and magnetic beads has been developed to detect endotoxin. The endotoxin-conjugated sandwich complex on magnetic beads was observed by scanning confocal laser microscopy. The resulting magnetic aptasensor rapidly detected (<1 min) endotoxin within a broad dynamic detection range of 10(-8) to 10(0)mg/ml in the presence of bovine serum albumin (BSA), RNA, sucrose, and glucose, which are most likely to coexist with endotoxin in the majority of biological liquids. Only 2 μl of magnetic aptasensor was required to quantify the endotoxin solution. Furthermore, the magnetic aptasensor could be regenerated seven times and still presented an outstanding response to the endotoxin solution. Therefore, the magnetic aptasensor exhibited high sensitivity, selectivity, and reproducibility, thereby serving as a powerful tool for the quality control and high-throughput detection of endotoxin in the food and pharmaceutical industries.Entities:
Keywords: Aptasensor; Endotoxin; Flow cytometry; Magnetic beads
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Year: 2014 PMID: 25172133 DOI: 10.1016/j.ab.2014.08.018
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365