Evidence map›Paper›PMID 41157339›Full record

ArticleSensors (Basel, Switzerland)2025

Interplay of the Mass Transport and Reaction Kinetics for Lateral Flow Immunoassay Integrated on Lab-on-Disc.

Snehan Peshin, Anthony Gavin, Nakajima Rie, Aarti Jain, Philip Felgner, Marc J Madou, Lawrence Kulinsky

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 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.

Snehan PeshinDepartment of Mechanical and Aerospace Engineering, University of California, Irvine, CA 92697, USA.ORCID 0000-0001-8137-9996
Anthony GavinDepartment of Chemistry, Saddleback College, Mission Viejo, CA 92692, USA.
Nakajima RieDepartment of Physiology and Biophysics, School of Medicine, University of California, Irvine, CA 92697, USA.ORCID 0000-0002-6026-3342
Aarti JainDepartment of Physiology and Biophysics, School of Medicine, University of California, Irvine, CA 92697, USA.
Philip FelgnerDepartment of Physiology and Biophysics, School of Medicine, University of California, Irvine, CA 92697, USA.ORCID 0000-0002-4117-8505
Marc J MadouDepartment of Mechanical and Aerospace Engineering, University of California, Irvine, CA 92697, USA.ORCID 0000-0003-4847-3117
Lawrence KulinskyDepartment of Mechanical and Aerospace Engineering, University of California, Irvine, CA 92697, USA.ORCID 0000-0002-1176-3578

Funding

Autonomous Medical Devices Incorporated NA
6 · The paper itself

Abstract

Lateral Flow Assays (LFAs) are ubiquitous test platforms due to their affordability and simplicity but are often limited by low sensitivity and lack of flow control. The present work demonstrates the combination of LFAs with centrifugal microfluidic platforms that allows for enhancement of LFAs' sensitivity via the increase in the dwell time of the analyte at the test line as well as by passing a larger sample volume through the LFA strip. The rate of advancement of the liquid front in the radially positioned NC strip is retarded by the centrifugal force generated on spinning disc; therefore, the dwell time of the liquid front above the test line of LFA is increased. Additionally, integrating a waste reservoir enables passive replenishment of additional sample volume increases total probed volume by approximately 20% (from 50 μL to 60 μL). Comprehensive analysis, including COMSOL multiphysics simulation, was performed to deduce the importance of parameters such as channel height (100-300 μm), disc spin rate (0-2000 rpm), and reaction kinetics (fast vs. slow binding kinetics). The analysis was validated by the experimental observation of the slower-reacting CD79b protein on the test strip. For slower-reacting targets like CD79b, fluorescence intensity increased by ~40% compared to the static LFA. A new merit number, TRc (Transport Reaction Constant), is introduced, which refines the traditional Damköhler number (Da) by including the thickness of the liquid layer (such as the height of the microchannel), which affects the final sensitivity of the assays and is designed to reflect the role channel height plays for surface-based assays (in contrast to the bulk assays).

Indexed as

Lab-On-A-Chip DevicesMicrofluidic Analytical TechniquesHumansImmunoassayKineticscentrifugal microfluidicslateral flow assaysurface reaction kineticstransport-reaction constant (TRc)

Identifiers

PMID41157339
PMCPMC12567277

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.