ArticleScientific reports2025
DNAzyme-based colorimetric biosensor for rapid detection of Shigella flexneri.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Recent Progress in Nanoparticle-Based Biosensors for MonitoringBiosensors · 2026Review
- Ultrasensitive colorimetric detection of Salmonella typhimurium using a magnetic graphene oxide-assisted DNAzyme aptasensor.Mikrochimica acta · 2025Article
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Shigella flexneri, a formidable gram-negative bacterium, that triggers the most contagious form of shigellosis through bloody diarrhea, presenting a significant threat. As a severe foodborne pathogen, it underscores the need for intensified research into more effective prevention strategies and heightened public health awareness. The traditional methods used to detect S. flexneri are time-consuming and inconvenient. As a result, there is a need for accurate and rapid diagnostics in food and water samples. The experimental methods involved modifying S. flexneri-specific HGD-aptamer and employing single-walled carbon nanotubes to develop a colorimetric detection assay exploiting DNAzyme. The HGD-aptamer-SWCNT complex binds specifically to S. flexneri cells, resulting in a detectable colorimetric response in a test sample involving enzymatic reactions. The assay's efficacy was validated through sensitivity and specificity evaluations, which demonstrated a detection limit of 51 CFU/mL and selective detection of the target with no signal in different bacterial environments. Comparative analysis with PCR-based methods confirmed the assay's performance, highlighting its potential as a rapid, cost-effective, and user-friendly diagnostic tool. This study introduces an innovative approach to identifying S. flexneri, which has the potential to improve food safety, environmental monitoring, and public health.
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Registered trials
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