4.5 Article

Microchip electrophoresis separation of a panel of preterm birth biomarkers

Journal

ELECTROPHORESIS
Volume 39, Issue 18, Pages 2300-2307

Publisher

WILEY
DOI: 10.1002/elps.201800078

Keywords

Disease diagnosis; Integrated microfluidics; Point-of-care diagnostics; Rapid analysis; Surface photografting

Funding

  1. National Institutes of Health [R01 EB006124]
  2. Roland K. Robins graduate research fellowship through the Department of Chemistry and Biochemistry at Brigham Young University
  3. Brigham Young University
  4. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [R01EB006124] Funding Source: NIH RePORTER

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Preterm birth (PTB) is responsible for over one million infant deaths annually worldwide. Often, the first and only indication of PTB risk is the onset of early labor. Thus, there is an urgent need for an early PTB risk diagnostic that is inexpensive, reliable, and robust. Here, we describe the development of a microchip electrophoresis (mu CE) method for separating a mixture of six PTB protein and peptide biomarkers present in maternal blood serum. mu CE devices were photografted with a poly(ethylene glycol) diacrylate surface coating to regulate EOF and reduce nonspecific analyte adsorption. Separation conditions including buffer pH, buffer concentration, and applied electric field were varied to improve biomarker peak resolution while minimizing deleterious effects like Joule heating. In this way, it was possible to separate six PTB biomarkers, the first mu CE separation of this biomarker panel. LODs were also measured for each of the six PTB biomarkers. In the future, this mu CE separation can be integrated with upstream maternal blood serum sample preparation steps to yield a complete PTB risk diagnosis microdevice.

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