Davic Andrew, Cascio Michael
Department of Chemistry and Biochemistry, Duquesne University, Pittsburgh, PA 15282, USA.
Metabolites. 2021 Feb 24;11(3):130. doi: 10.3390/metabo11030130.
The inherent trace quantity of primary fatty acid amides found in biological systems presents challenges for analytical analysis and quantitation, requiring a highly sensitive detection system. The use of microfluidics provides a green sample preparation and analysis technique through small-volume fluidic flow through micron-sized channels embedded in a polydimethylsiloxane (PDMS) device. Microfluidics provides the potential of having a micro total analysis system where chromatographic separation, fluorescent tagging reactions, and detection are accomplished with no added sample handling. This study describes the development and the optimization of a microfluidic-laser induced fluorescence (LIF) analysis and detection system that can be used for the detection of ultra-trace levels of fluorescently tagged primary fatty acid amines. A PDMS microfluidic device was designed and fabricated to incorporate droplet-based flow. Droplet microfluidics have enabled on-chip fluorescent tagging reactions to be performed quickly and efficiently, with no additional sample handling. An optimized LIF optical detection system provided fluorescently tagged primary fatty acid amine detection at sub-fmol levels (436 amol). The use of this LIF detection provides unparalleled sensitivity, with detection limits several orders of magnitude lower than currently employed LC-MS techniques, and might be easily adapted for use as a complementary quantification platform for parallel MS-based omics studies.
生物系统中存在的痕量一级脂肪酸酰胺对分析和定量分析提出了挑战,需要高灵敏度的检测系统。微流控技术通过小体积流体在嵌入聚二甲基硅氧烷(PDMS)装置中的微米级通道中流动,提供了一种绿色的样品制备和分析技术。微流控技术具有实现微全分析系统的潜力,在该系统中,色谱分离、荧光标记反应和检测无需额外的样品处理即可完成。本研究描述了一种微流控激光诱导荧光(LIF)分析检测系统的开发和优化,该系统可用于检测超痕量水平的荧光标记一级脂肪酸胺。设计并制造了一种基于液滴流动的PDMS微流控装置。液滴微流控技术能够快速、高效地进行芯片上的荧光标记反应,无需额外的样品处理。优化后的LIF光学检测系统能够检测亚飞摩尔水平(436 阿摩尔)的荧光标记一级脂肪酸胺。这种LIF检测技术具有无与伦比的灵敏度,检测限比目前使用的液相色谱-质谱(LC-MS)技术低几个数量级,并且可能很容易被用作基于质谱的平行组学研究的补充定量平台。