Evidence map›Paper›PMID 41693768›Full record

ArticleSensors & diagnostics2025

A new sequential dual flow lab-on-a-chip with a lyophilized one-component chemiluminescence substrate for high-sensitive microchannel lateral flow assay (mLFA).

Supreeth Setty, Heeyeong Jang, Jungyoup Han, Joo Youn Park, Nogi Park, Keun Seok Seo, Chong Ahn

Abstract read
In one paragraph

Article in Sensors & diagnostics, 2025. 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

7 authors.

Supreeth SettyMicroSystems and BioMEMS Laboratory, Department of Electrical and Computer Engineering, University of Cincinnati Cincinnati OH 45221 USA ahnch@ucmail.uc.edu.ORCID https://orcid.org/0009-0005-6228-8454
Heeyeong JangMicroSystems and BioMEMS Laboratory, Department of Electrical and Computer Engineering, University of Cincinnati Cincinnati OH 45221 USA ahnch@ucmail.uc.edu.ORCID https://orcid.org/0009-0006-4043-1587
Jungyoup HanMiCo BioMed USA Inc., Skillman NJ 08558 USA.ORCID https://orcid.org/0009-0005-5165-1051
Joo Youn ParkDepartment of Comparative Biomedical Sciences, College of Veterinary Medicine, Mississippi State University Mississippi State MS 39762 USA seo@cvm.msstate.edu.ORCID https://orcid.org/0000-0002-8375-0178
Nogi ParkDepartment of Comparative Biomedical Sciences, College of Veterinary Medicine, Mississippi State University Mississippi State MS 39762 USA seo@cvm.msstate.edu.
Keun Seok SeoDepartment of Comparative Biomedical Sciences, College of Veterinary Medicine, Mississippi State University Mississippi State MS 39762 USA seo@cvm.msstate.edu.
Chong AhnMicroSystems and BioMEMS Laboratory, Department of Electrical and Computer Engineering, University of Cincinnati Cincinnati OH 45221 USA ahnch@ucmail.uc.edu.ORCID https://orcid.org/0000-0002-1006-7204

Funding

Tracking and Evaluation CoreU54GM115428 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI HALL, JOHN E · 2016 to 2025
$38.2M
NIGMS NIH HHS U54 GM115428
6 · The paper itself

Abstract

Recently, there has been a growing demand for the development of lab-on-a-chip (LOC) platforms with new assays and detection protocols for point-of-care-test (POCT) applications. So far, chemiluminescence (CL) detection-based immunoassays have shown promising performance for the high-sensitive POCT, but they require automated machines or multiple manual steps to perform the CL-based assay. In this work, a fully automated CL-based immunoassay was developed using a new sequential dual flow LOC with on-chip lyophilized CL substrate, and then a highly specific and sensitive immunoassay using a pair of single chain variable fragment (scFv) capture and detection antibodies was successfully performed. The concept of sequential and automatic control of dual flows, which was strongly desired for ensuring that the reconstituted detection antibody conjugated with horseradish peroxidase flowed first through the reaction zones and then the reconstituted CL substrate flowed, was newly developed and implemented on the LOC. In addition, a new one-component CL substrate in liquid format was introduced and lyophilized for the on-chip lyophilized substrate, developing a new lyophilization process. To evaluate the assay performance on the developed new LOC platform, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was chosen as a demonstration vehicle. The nucleocapsid (N) protein of SARS-CoV-2 was analyzed using the custom-developed scFv antibody pair from a phage display library system, which showed a better limit of detection (LoD) over the commercially available rapid diagnostic test (RDT) kits for detecting SARS-CoV-2. Finally, a portable reader for reading the CL signal from the CL-based microchannel lateral flow assay (CL-mLFA) was developed and used for evaluating the performance of the SARS-CoV-2 assay on the developed LOC platform. An LoD of approximately 1.6 ng mL

Identifiers

PMID41693768
PMCPMC12895396

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.