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Pre-concentration by liquid intake by paper (P-CLIP): a new technique for large volumes and digital microfluidics†

Microfluidic platforms are an attractive option for incorporating complex fluid handling into low-cost and rapid diagnostic tests. A persistent challenge for microfluidics, however, is the mismatch in the “world-to-chip” interface – it is challenging to detect analytes present at low concentrations...

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Detalles Bibliográficos
Autores principales: Rackus, Darius, de Campos, Richard P. S., Chan, Calvin, Karcz, Maria M., Seale, Brendon, Narahari, Tanya, Dixon, Christopher, Chamberlainab, M. Dean, Wheeler, Aaron R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734381/
https://www.ncbi.nlm.nih.gov/pubmed/28604891
http://dx.doi.org/10.1039/c7lc00440k
Descripción
Sumario:Microfluidic platforms are an attractive option for incorporating complex fluid handling into low-cost and rapid diagnostic tests. A persistent challenge for microfluidics, however, is the mismatch in the “world-to-chip” interface – it is challenging to detect analytes present at low concentrations in systems that can only handle small volumes of sample. Here we describe a new technique termed pre-concentration by liquid intake by paper (P-CLIP) that addresses this mismatch, allowing digital microfluidics to interface withvolumes on the order of hundreds of microliters. In P-CLIP, a virtual microchannel is generated to pass a large volume through the device; analytes captured on magnetic particles can be isolated and then resuspended into smaller volumes for further processing and analysis. We characterize this method and demonstrate its utility with an immunoassay for Plasmodiumfalciparum lactate dehydrogenase, a malaria biomarker, and propose that the P-CLIPstrategy may be useful for a wide range of applications that are currently limited by low-abundance analytes.