Evidence map›Paper›PMID 41885508›Full record

ArticleThe Analyst2026

Lyophilised colourimetric LAMP for visual readout with dual colour indicators.

Kenny Malpartida-Cardenas, Oliver W Stringer, Matthew L Cavuto, Alison Holmes, Jesus Rodriguez-Manzano

Abstract read
In one paragraph

Article in The Analyst, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Kenny Malpartida-CardenasDepartment of Infectious Disease, Imperial College London, London, UK. k.malpartida-cardenas16@imperial.ac.uk.ORCID http://orcid.org/0000-0002-3874-8810
Oliver W StringerDepartment of Infectious Disease, Imperial College London, London, UK. k.malpartida-cardenas16@imperial.ac.uk.ORCID http://orcid.org/0000-0001-9345-5642
Matthew L CavutoDepartment of Infectious Disease, Imperial College London, London, UK. k.malpartida-cardenas16@imperial.ac.uk.ORCID http://orcid.org/0000-0002-6104-6083
Alison HolmesDepartment of Infectious Disease, Imperial College London, London, UK. k.malpartida-cardenas16@imperial.ac.uk.ORCID http://orcid.org/0000-0001-5554-5743
Jesus Rodriguez-ManzanoDepartment of Infectious Disease, Imperial College London, London, UK. k.malpartida-cardenas16@imperial.ac.uk.ORCID http://orcid.org/0000-0002-2583-8366

Funding

Wellcome Trust
6 · The paper itself

Abstract

Loop-mediated isothermal amplification (LAMP) is increasingly recognised as a practical alternative to PCR for pathogen detection, offering rapid turnaround time, a constant operating temperature, and compatibility with a wide range of detection methods. Colourimetric LAMP has gained popularity due to its potential for instrument-free readout, making it suitable for molecular diagnostics in low-resource settings. Despite these advantages, its adoption at the point-of-care remains limited as it has been widely used in liquid format and therefore restricted to the availability of cold-chain storage and trained personnel. This work introduces the development and optimisation of ready-to-use lyophilised colourimetric LAMP (lyo-cLAMP) that does not require cold-chain, additional reagents, or manual intervention beyond the addition of extracted nucleic acids from a sample, which indicates the presence of a target of interest by colour change after amplification. A variety of pH and metal indicators were screened and combined to evaluate their synergy, identifying four combinations with high discrimination between positive and negative amplification. The performance of lyo-cLAMP was assessed with synthetic SARS-CoV-2 RNA, comparing it to the liquid format and achieving the same limit-of-detection. Lastly, the translation of lyo-cLAMP to diagnostic applications was demonstrated by screening positive SARS-CoV-2 residual clinical samples, achieving high accuracy. The developed lyo-cLAMP is compatible with any LAMP assay, allowing for rapid adaptation to new targets, which is particularly valuable in outbreak scenarios.

Indexed as

ColorimetryCOVID-19Molecular Diagnostic TechniquesNucleic Acid Amplification TechniquesSARS-CoV-2ColorFreeze DryingHumansHydrogen-Ion ConcentrationRapid Diagnostic TestsRNA, ViralRNA, Viral

Identifiers

PMID41885508
PMCPMC13020249

What OpenQuestion holds

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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.