ReviewBiosensors2026
Evolution of Next-Generation Multiplex Lateral Flow Immunoassays: From Engineered Nanomaterials to AI-Driven Detection.
Review in Biosensors, 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
3 authors.
Funding
Abstract
Decentralized diagnostics is undergoing a transformative shift from qualitative screening to high-precision quantification, driven by the clinical demand for rapid, point-of-care (POC) syndromic triage. Multiplexed lateral flow immunoassays (mLFIAs) serve as the foundational platform for this transition. However, their performance is limited by systemic factors such as fluidic lag, conjugate depletion, and spectral crosstalk. This review evaluates recent advances in engineered nanomaterials and artificial intelligence (AI)-driven detection as the dual pillars of next-generation multiplexing. The review covers different types of nanomaterial reporters-such as multicolor quantum dots, surface-enhanced Raman scattering nanotags, upconversion nanoparticles, surface-modified magnetic nanoparticles, and fluorescent nanodiamonds-that help address analytical challenges in lateral flow assays. We then discuss AI and machine learning methods, including convolutional neural networks, support vector machines, random forests, and transfer learning, that convert raw multi-channel signals into useful clinical data. Finally, we highlight the main challenges that still need to be addressed before these platforms can become WHO-ASSURED-compliant POC devices. The combination of engineered nanomaterial reporters and computational intelligence is transforming lateral flow assays into quantitative tools that can provide lab-quality clinical information at the POC.
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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 OpenQuestion graph.