Enabling a microfluidic immunoassay for the developing world by integration of on-card dry reagent storage

As part of an effort to create a point-of-care diagnostic system for the developing world, we present a microfluidic flow-through membrane immunoassay with on-card dry reagent storage. By preserving reagent function, the storage and reconstitution of anhydrous reagents enables the devices to remain...

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Bibliographic Details
Published in:Lab on a chip 2008-01, Vol.8 (12), p.2038-2045
Main Authors: Stevens, Dean Y, Petri, Camille R, Osborn, Jennifer L, Spicar-Mihalic, Paolo, McKenzie, Katherine G, Yager, Paul
Format: Article
Language:English
Subjects:
Animals
Desiccation
Developing Countries
Immunoassay - instrumentation
Immunoassay - methods
Indicators and Reagents - chemistry
Microfluidics - instrumentation
Microfluidics - methods
Models, Biological
Plasmodium
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Summary:As part of an effort to create a point-of-care diagnostic system for the developing world, we present a microfluidic flow-through membrane immunoassay with on-card dry reagent storage. By preserving reagent function, the storage and reconstitution of anhydrous reagents enables the devices to remain viable in challenging, unregulated environmental conditions. The assay takes place on a disposable laminate card containing both a porous membrane patterned with capture molecules and a fibrous pad containing an anhydrous analyte label. To conduct the assay, the card is placed in an external pumping and imaging instrument capable of delivering sample and rehydrated reagent to the assay membrane at controlled flow rates to generate quantitative results. Using the malarial antigen Plasmodium falciparum histidine-rich protein II (PfHRP2) as a model, we demonstrate selection of dry storage conditions, characterization of reagent rehydration, and execution of an automated on-card assay. Gold-antibody conjugates dried in a variety of sugar matrices were shown to retain 80-96% of their activity after 60 days of storage at elevated temperatures, and the release profile of the reconstituted reagent was characterized under flow in microfluidic channels. The system gave a detection limit in the sub-nanomolar range in under nine minutes, showing the potential to expand into quantitative, multi-analyte analysis of human blood samples.
ISSN:1473-0197
1473-0189
DOI:10.1039/b811158h