Aug 2026· Analytical Chemistry· Vol 98 32, pp.
23672-23683
· 0 citations· 42 references
Medicine
Abstract
Species fingerprinting is crucial to ensure food safety and human health, which requires a rapid, simple, multiplex, and field-deployable detection technique. In response, a lab-on-a-disc microfluidic chip with CRISPR/Cas12a that integrates target preamplification and signal readout enhanced by tetrahedral DNA frameworks (TDFs) has been developed in this study. This platform automates the workflow from recombinase polymerase amplification (RPA) through signal readout. In addition, a portable heating module was developed specifically for colorimetric detection, providing a complete field-deployable solution. The performance of the CRISPR/Cas12a platform was evaluated by detecting cow's milk adulteration in buffalo milk. The platform demonstrated high sensitivity, achieving detection limits of 1% (v/v) and 5% (v/v) for fluorescence and colorimetric detection within 1 h, respectively. The results agree well with those from real-time quantitative polymerase chain reaction (qPCR) in real-sample analysis. The integrated CRISPR/Cas12a-based duplex detection platform features high sensitivity and specificity, reaction automation, minimal aerosol contamination risk, and decentralized operation, which demonstrates significant potential for field-deployable species fingerprinting and risk prediction.
Objective. Molecular methods have revolutionized the detection of foodborne pathogens, enabling rapid and reliable identification following a pre-enrichment step. Among the available techniques for the detection of Salmonella spp., Loop-Mediated Isothermal Amplification (LAMP) stands out for its speed, simplicity, and...
A. Mancusi· Italian Journal of Food Safe...· 0 citations
The clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated proteins (Cas) system enables sensitive and specific biomolecular detection due to its programmability, high fidelity, and signal amplification. Herein, a novel universal CRISPR/Cas12a-G4 DNAzyme-TMB (Cas-GT) enzymatic biosensi...
Huisi Qin, Jing-Xuan Liu, Yang Luo et al.· In Analysis· 0 citations
Mycobacterium tuberculosis
remains a major global public health threat, imposing significant socioeconomic burdens. Current molecular diagnostics rely heavily on nucleic acid extraction and specialized equipment, which limits their use in resource-limited settings. We developed a rapid, sensitive platform suitable f...
Jia-Yin Xing, Xiang-Xiang Zhao, Gao-Jie Wang et al.· Frontiers in Microbiology· 0 citations
CATNAP (Cas trans -nuclease detection of amplified products), a method that integrates isothermal linear DNA amplification with Cas12a detection in a single reaction, bridges the sensitivity gap in CRISPR diagnostics while maintaining simplicity, making accurate disease detection more accessible in resource-limited setti...
Selma Sinan, Remy M. Kooistra, Karunya Rajaraman et al.· 0 citations
The design principles and working mechanisms of cascaded CRISPR strategies, encompassing Enzyme-Coupled cascades, Multi-effector class 2 CRISPR cascades, and Type III CRISPR-mediated cascades are introduced, including integration with digital detection platforms and AI-assistant algorithms are discussed.
Ruo-Nan He, Lu Miao, Rui-Jie Deng et al.· Biosensors & bioelectronics· 0 citations
Monitoring antimicrobial resistance (AMR) in aquatic systems is essential for tracking resistance mechanisms and identifying microbial sources. Here, we present a dual-module electrochemical sensing platform that integrates a gold-electrode-based RPA–CRISPR/Cas12a biosensor for detecting antibiotic resistance genes (...
Yu-Wei Pan, Wen-Liang Li, J. Cooper et al.· Analytical Chemistry· 0 citations
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