Related Experiment Video
Updated: Oct 18, 2026

Phthalic Acid Ester-Binding DNA Aptamer Selection, Characterization, and Application to an Electrochemical Aptasensor
Published on: March 21, 2018
Wide-range and sensitive detection of LPS using a transporter@liposome enhanced electrochemical aptasensor
Xinyu Hu1, Shukai Song1, Ruyu Lin1
1Zhejiang Key Laboratory of Smart Low-voltage Apparatus and New Energy Application, Key Laboratory of Micro-Nano Optoelectronic Devices (Wenzhou), College of Electrical and Electronic Engineering, Wenzhou University, Wenzhou, 325035, China.
Abstract:
Stringent detection of lipopolysaccharide (LPS) is crucial for ensuring drug and food safety, enabling effective control of endotoxin contamination in pharmaceuticals and food. Given the wide variation in LPS concentrations across different matrices, the assay methods for LPS are extremely needed combining a wide dynamic range with high sensitivity. Employing metallohelicate embedded liposomal for electrochemical sensor modification, a novel strategy is developed for high-performance detection of LPS with aptamer probes. Metallohelicates are non-destructively incorporated into the lipid bilayer and act as a selective chloride ion transporter, enhancing the influx of chloride ions across the membrane, thereby increasing the permeability of the liposomal membrane and its conductivity. The current response is therefore amplified, significantly improving the sensitivity and reducing the limit of detection (LOD). The extensive surface area of liposomal spherical structure with high-density aptamers also greatly enhances its capacity to adsorb high-concentration targets. This aptasensor achieves a LOD of 0.44 fg/mL and provides an extremely wide dynamic range up to 1 μg/mL, with satisfied recovery and accuracy for LPS detection in pharmaceutical injections and food matrices.
Related Concept Videos
Enzyme-Linked Immunosorbent Assay
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen. Enzyme-substrate reaction allows the antigen to be visualized or quantified.
Formation of Lipopolysaccharides

