Holmes David, She Joseph K, Roach Peter L, Morgan Hywel
School of Electronics and Computing Science, University of Southampton, Highfield, Southampton, UK SO17 1BJ.
Lab Chip. 2007 Aug;7(8):1048-56. doi: 10.1039/b707507n. Epub 2007 Jun 14.
A microfabricated flow cytometer has been developed for the analysis of micron-sized polymer beads onto which fluorescently labelled proteins have been immobilised. Fluorescence measurements were made on the beads as they flowed through the chip. Binding of antibodies to surface-immobilised antigens was quantitatively assayed using the device. Particles were focused through a detection zone in the centre of the flow channel using negative dielectrophoresis. Impedance measurements of the particles (at 703 kHz) were used to determine particle size and to trigger capture of the fluorescence signal. Antibody binding was measured by fluorescence at single and dual excitation wavelengths (532 nm and 633 nm). Fluorescence compensation techniques were implemented to correct for spectral overspill between optical detection channels. The data from the microfabricated flow cytometer was shown to be comparable to that of a commercial flow cytometer (BD-FACSAria).
一种用于分析固定有荧光标记蛋白质的微米级聚合物微珠的微型化流式细胞仪已被开发出来。当微珠流过芯片时,对其进行荧光测量。使用该装置对抗体与表面固定抗原的结合进行了定量分析。通过负介电泳将颗粒聚焦通过流动通道中心的检测区。利用颗粒的阻抗测量(703 kHz)来确定颗粒大小并触发荧光信号的捕获。通过单激发波长(532 nm)和双激发波长(633 nm)的荧光测量抗体结合情况。采用荧光补偿技术校正光学检测通道之间的光谱溢出。结果表明,微型化流式细胞仪的数据与商用流式细胞仪(BD-FACSAria)的数据具有可比性。