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Digital microfluidic platform for the detection of rubella infection and immunity: a proof of concept.
Ng, Alphonsus H C; Lee, Misan; Choi, Kihwan; Fischer, Andrew T; Robinson, John M; Wheeler, Aaron R.
Affiliation
  • Ng AH; Institute of Biomaterials and Biomedical Engineering, Donnelly Centre for Cellular and Biomolecular Research, Toronto, ON, Canada;
  • Lee M; Innis College, and Donnelly Centre for Cellular and Biomolecular Research, Toronto, ON, Canada;
  • Choi K; Donnelly Centre for Cellular and Biomolecular Research, Toronto, ON, Canada; Department of Chemistry, University of Toronto, Toronto, ON, Canada;
  • Fischer AT; Abbott Diagnostics, Irving, TX;
  • Robinson JM; Abbott Diagnostics, Abbott Park, IL.
  • Wheeler AR; Institute of Biomaterials and Biomedical Engineering, Donnelly Centre for Cellular and Biomolecular Research, Toronto, ON, Canada; Department of Chemistry, University of Toronto, Toronto, ON, Canada; aaron.wheeler@utoronto.ca.
Clin Chem ; 61(2): 420-9, 2015 Feb.
Article in En | MEDLINE | ID: mdl-25512641
BACKGROUND: Whereas disease surveillance for infectious diseases such as rubella is important, it is critical to identify pregnant women at risk of passing rubella to their offspring, which can be fatal and can result in congenital rubella syndrome (CRS). The traditional centralized model for diagnosing rubella is cost-prohibitive in resource-limited settings, representing a major obstacle to the prevention of CRS. As a step toward decentralized diagnostic systems, we developed a proof-of-concept digital microfluidic (DMF) diagnostic platform that possesses the flexibility and performance of automated immunoassay platforms used in central facilities, but with a form factor the size of a shoebox. METHODS: DMF immunoassays were developed with integrated sample preparation for the detection of rubella virus (RV) IgG and IgM. The performance (sensitivity and specificity) of the assays was evaluated with serum and plasma samples from a commercial antirubella mixed-titer performance panel. RESULTS: The new platform performed the essential processing steps, including sample aliquoting for 4 parallel assays, sample dilution, and IgG blocking. Testing of performance panel samples yielded diagnostic sensitivity and specificity of 100% and 100% for both RV IgG and RV IgM. With 1.8 µL sample per assay, 4 parallel assays were performed in approximately 30 min with <10% mean CV. CONCLUSIONS: This proof of concept establishes DMF-powered immunoassays as being potentially useful for the diagnosis of infectious disease.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rubella / Rubella virus / Immunoglobulin G / Immunoglobulin M / Immunoassay / Microfluidic Analytical Techniques / Antibodies, Viral Type of study: Diagnostic_studies / Evaluation_studies / Prognostic_studies Limits: Female / Humans / Pregnancy Language: En Journal: Clin Chem Journal subject: QUIMICA CLINICA Year: 2015 Document type: Article Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Rubella / Rubella virus / Immunoglobulin G / Immunoglobulin M / Immunoassay / Microfluidic Analytical Techniques / Antibodies, Viral Type of study: Diagnostic_studies / Evaluation_studies / Prognostic_studies Limits: Female / Humans / Pregnancy Language: En Journal: Clin Chem Journal subject: QUIMICA CLINICA Year: 2015 Document type: Article Country of publication: United kingdom