Related Experiment Video
Updated: Aug 6, 2026

Colorimetric Paper-based Detection of Escherichia coli, Salmonella spp., and Listeria monocytogenes from Large Volumes of Agricultural Water
Published on: June 9, 2014
Paper-Based Chip Platform: PCR-SERS-LFA Integration for On-Site Coastal Harmful Microorganism Detection
Qishuo Wang1,2, Yunqing Wang1,2,3, Longwen Fu1,2
1Shandong Key Laboratory of Coastal Zone Environmental Processes and Ecological Security, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai264003China.
This study introduces a portable paper-based platform for rapid on-site detection of harmful algal blooms and pathogens using polymerase chain reaction (PCR) and surface-enhanced Raman scattering (SERS). The integrated system provides accurate results within 30 minutes, enhancing environmental monitoring and public health surveillance.
Area of Science:
- Environmental Science
- Biotechnology
- Analytical Chemistry
Background:
- Harmful algal blooms (HABs) and pathogenic microorganisms pose significant threats to coastal ecosystems and public health.
- Rapid, field-deployable detection methods are crucial for timely intervention and risk mitigation.
Purpose of the Study:
- To develop an integrated, paper-based platform for simultaneous on-site detection of HABs and pathogenic microorganisms.
- To combine Polymerase Chain Reaction (PCR), Surface-Enhanced Raman Scattering (SERS), and Lateral Flow Assay (LFA) for nucleic acid detection.
- To achieve rapid, portable, and contamination-free detection within 30 minutes.
Main Methods:
- Integration of a miniature thermal cycler, lyophilized paper-based reaction chambers, and a capillary-driven detection pen.
- Utilizing SERS and Lateral Flow Assay (LFA) for dual-mode nucleic acid detection.
- Field validation using environmental samples from a coastal bathing beach.
Main Results:
- Achieved limits of detection of 10^1-10^2 copies/μL (SERS) and 10^3-10^4 copies/μL (visualization) for target organisms.
- Complete amplification and detection within 30 minutes.
- Demonstrated comparable performance to laboratory-based quantitative PCR (qPCR) in field validation.
- Successfully identified Ulva prolifera micropropagules and enabled large-scale mapping of overwintering zones.
Conclusions:
- The developed integrated paper-based platform offers a portable and rapid solution for on-site detection of HABs and pathogens.
- The platform shows comparable performance to gold-standard methods, supporting environmental monitoring and public health surveillance.
- This technology facilitates timely identification of ecological threats and supports effective management strategies.
Related Concept Videos
iChip
Microbial Biosensors
Automated Microbial Diagnostics

