Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT, USA.
Electrophoresis. 2018 Sep;39(18):2300-2307. doi: 10.1002/elps.201800078. Epub 2018 Jun 1.
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 (μCE) method for separating a mixture of six PTB protein and peptide biomarkers present in maternal blood serum. μCE 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 μCE separation of this biomarker panel. LODs were also measured for each of the six PTB biomarkers. In the future, this μCE separation can be integrated with upstream maternal blood serum sample preparation steps to yield a complete PTB risk diagnosis microdevice.
早产(PTB)每年导致全球超过 100 万婴儿死亡。通常,PTB 风险的第一个也是唯一迹象是早期分娩的开始。因此,迫切需要一种廉价、可靠和稳健的早期 PTB 风险诊断方法。在这里,我们描述了一种微芯片电泳(μCE)方法的开发,用于分离存在于母体血清中的六种 PTB 蛋白和肽生物标志物的混合物。μCE 设备通过光接枝聚乙二醇二丙烯酸酯表面涂层来调节 EOF 并减少非特异性分析物吸附。改变分离条件,包括缓冲液 pH 值、缓冲液浓度和施加的电场,以提高生物标志物峰的分辨率,同时最小化焦耳加热等有害影响。通过这种方式,可以分离六种 PTB 生物标志物,这是该生物标志物组的第一次 μCE 分离。还测量了六种 PTB 生物标志物中的每一种的 LOD。将来,可以将这种 μCE 分离与上游母体血清样本制备步骤集成,以获得完整的 PTB 风险诊断微器件。