Center for Bio/Molecular Science and Engineering, Naval Research Laboratory, Washington, DC 20375-5348, USA.
Anal Bioanal Chem. 2010 Nov;398(5):1871-81. doi: 10.1007/s00216-010-4019-7. Epub 2010 Jul 25.
With a view toward developing a rugged microflow cytometer, a sheath flow system was micromachined in hard plastic (polymethylmethacrylate) for analysis of particles and cells using optical detection. Six optical fibers were incorporated into the interrogation region of the chip, in which hydrodynamic focusing narrowed the core stream to ~35 μm × 40 μm. The use of a relatively large channel at the inlet as well as in the interrogation region (375 μm × 125 μm) successfully minimized the risk of clogging. The device could withstand pressures greater than 100 psi without leaking. Assays using both coded microparticles and cells were demonstrated using the microflow cytometer. Multiplexed immunoassays detected nine different bacteria and toxins using a single mixture of coded microspheres. A549 cancer cells processed with locked nucleic acid probes were evaluated using fluorescence in situ hybridization.
为了开发一种坚固耐用的微流控细胞仪,我们在硬塑料(聚甲基丙烯酸甲酯)中微加工了一个鞘流系统,用于使用光学检测分析颗粒和细胞。在芯片的检测区域中集成了六根光纤,其中流体动力学聚焦将核心流缩小到约 35 μm×40 μm。在入口处以及检测区域(375 μm×125 μm)使用相对较大的通道成功地将堵塞的风险降到了最低。该设备在超过 100 psi 的压力下也不会发生泄漏。使用微流控细胞仪进行了编码微球和细胞的检测实验。使用编码微球的单一混合物,多重免疫分析可以检测到九种不同的细菌和毒素。使用荧光原位杂交法评估了用锁核酸探针处理的 A549 癌细胞。