Evidence map›Paper›PMID 42700408›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2026

Lab-in-a-Tube System Integrating Hierarchically Wrinkled Electrodes and DNAzyme-Functionalized Beads for Diagnosis of Clostridioides difficile Infection.

Survanshu Saxena, Soyeon Lee, Youngeun Choi, Jonathan L'Heureux-Hache, Jiaying Liu, Sadman Sakib, Sara M Imani, Marek Smieja, Yingfu Li, Todd Hoare and 1 more

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Survanshu Saxena *School of Biomedical Engineering, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0003-2333-7215
Soyeon Lee *Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0009-0007-0109-6285
Youngeun ChoiSchool of Biomedical Engineering, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0002-4442-4898
Jonathan L'Heureux-HacheDepartment of Engineering Physics, McMaster University, Hamilton, Canada.
Jiaying LiuDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0009-0008-0966-5865
Sadman SakibDepartment of Engineering Physics, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0001-7601-6680
Sara M ImaniDepartment of Mechanical Engineering, McMaster University, Hamilton, Canada.
Marek SmiejaDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0003-1655-3761
Yingfu LiSchool of Biomedical Engineering, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0002-7533-6743
Todd HoareSchool of Biomedical Engineering, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0002-5698-8463
Leyla SoleymaniSchool of Biomedical Engineering, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0003-4915-2999

Funding

Canada Research Chair programDorothy Killam FellowshipMITACS Accelerate InternshipNatural Sciences and Engineering Research Council of CanadaNew Frontiers for Research Fund (NFRF)Zentek
6 · The paper itself

Abstract

The diagnosis of bacterial infections remains slow because many existing methods rely on enrichment steps such as nucleic acid amplification or growth culture. RNA-cleaving DNAzymes offer a promising route to accelerate bacterial diagnosis because they can be selected and programmed to specifically recognize disease-causing bacteria and generate reporter DNA strands for signal readout. However, integrating DNAzymes into biosensors capable of analyzing complex biological matrices remains challenging, as matrix-associated interferents can destabilize DNAzymes, suppress catalytic activity, and compromise signal detection. Here, we integrate redox RNA-cleaving DNAzymes housed on antifouling magnetic beads with a lab-in-a-tube platform that incorporates hierarchically structured sensing electrodes within a tubular flow cell for enrichment-free detection of Clostridioides difficile in stool samples. The combination of antifouling magnetic beads and fluidic replenishment of DNA reporters across the hierarchical electrodes reduces nonspecific binding and enhances reporter capture efficiency, achieving a limit of detection as low as 1.3 × 10

Indexed as

Biosensing TechniquesClostridioides difficileClostridium InfectionsDNA, CatalyticElectrochemical TechniquesElectrodesFecesHumansLimit of DetectionDNA, CatalyticC. difficileDNAzymeselectrochemical biosensingmicrogel magnetic beadsstoolwrinkles

Identifiers

PMID42700408
PMCPMC13648893

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.