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Multiplexed SERS Detection of Microcystins with Aptamer-Driven Core-Satellite Assemblies
Xiaojun Luo1,2,3,4, Xingjuan Zhao1,3,4, Gregory Q Wallace1,3,4
1Département de chimie, Université de Montréal, C.P. 6128 Succ. Centre-Ville, Montréal, Quebec, Canada H3C 3J7.
We developed novel surface-enhanced Raman spectroscopy (SERS) aptasensors for sensitive detection of microcystins (MCs). These sensors enable simultaneous detection of MC-LR and MC-RR in water samples with high accuracy.
Area of Science:
- Environmental Science
- Analytical Chemistry
- Nanotechnology
Background:
- Microcystins (MCs) are potent toxins produced by cyanobacteria, posing risks to aquatic ecosystems and human health.
- Accurate and sensitive detection methods for MCs are crucial for environmental monitoring and risk assessment.
- Existing detection methods may lack the sensitivity, selectivity, or multiplexing capabilities required for real-world applications.
Purpose of the Study:
- To develop and characterize novel surface-enhanced Raman spectroscopy (SERS) aptasensors for the indirect detection of microcystin-LR (MC-LR) and microcystin-RR (MC-RR).
- To achieve individual or simultaneous detection of MC-LR and MC-RR in natural water and algal culture samples.
- To enhance sensor sensitivity and reduce the limit of detection (LOD) compared to existing SERS-based methods.
Main Methods:
- Fabrication of core-satellite nanostructures using Au@label@Ag@Au nanoparticles immobilized on asymmetric Au nanoflowers (AuNFs).
- Functionalization of nanoparticles with MC-LR and/or MC-RR aptamers for specific analyte binding.
- Utilizing the dissociation of aptamer-functionalized nanoparticles upon MC binding to induce a decrease in SERS signal for indirect detection.
- Employing finite-difference time-domain (FDTD) simulations to analyze electromagnetic field enhancement.
Main Results:
- Achieved significantly low LODs: 0.8 pM for individual MC-LR detection and 1.5 pM for MC-LR / 1.3 pM for MC-RR in multiplex detection.
- Demonstrated excellent selectivity and high recovery rates (96-105%) for MC-LR and MC-RR.
- Successfully monitored MC-LR production in *M. aeruginosa* cultures over one week, validating real-world applicability.
Conclusions:
- The developed SERS aptasensors offer a highly sensitive and selective platform for detecting MC-LR and MC-RR in environmental samples.
- The core-satellite nanostructure design enhances SERS signal, leading to improved detection limits.
- These aptasensors show great promise for routine monitoring of microcystin contamination in aquatic environments.
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