ReviewAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
Transport-Reaction-Signal Coupling in Lateral Flow Assays for Next-Generation Point-of-Care Diagnostics.
Review in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
Lateral flow assays (LFAs) remain central to point-of-care diagnostics because they combine low cost, portability, and operational simplicity. Emerging diagnostic demands, including low-abundance biomarkers, complex sample matrices, quantitative readout, and multiplexed analysis, increasingly expose limitations that cannot be solved by signal-label enhancement alone. This Review examines recent LFA advances through a three-phase framework that couples porous-material mass transfer, interfacial reaction engineering, and signal transduction. The framework clarifies how membrane and flow design regulate analyte delivery and residence time, how antibody orientation, reaction amplification, and hook-effect mitigation improve capture efficiency and dynamic range, and how advanced nanolabels, integrated readers, multiplexed formats, and AI/ML-supported design and analysis expand performance across the assay workflow. By distinguishing intrinsic performance gains from strategies that transfer complexity to reagents, devices, or software, this Review provides design principles for sensitive, quantitative, and translation-oriented LFA systems.
Indexed as
Identifiers
What Socratic holds
Registered trials
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 Socratic graph.