Department of Biotechnology and Bioengineering, Sandia National Laboratories, 7011 East Avenue, Livermore, CA 94551, USA.
University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555, USA.
Biosens Bioelectron. 2014 Apr 15;54:435-41. doi: 10.1016/j.bios.2013.11.012. Epub 2013 Nov 12.
We present advancements in microfluidic technology for rapid detection of as few as 10 rickettsial organisms in complex biological samples. An immuno-reactive filter, macroporous polyacrylamide monolith (PAM), fabricated within a microfluidic channel enhances solid-phase immuno-capture, staining and detection of targeted bacteria. Bacterial cells in samples flowing through the channel are forced to interact with the PAM filter surface due to size exclusion, overcoming common transport and kinetic limitations for rapid (min), high-efficiency (~100%) capture. In the process, targeted cells in sample volumes of 10 μl to >100 μl are concentrated within a sub-50 nl region at the PAM filter edge in the microchannel, thus concentrating them over 1000-fold. This significantly increases sensitivity, as the hydrophilic PAM also yields low non-specific immuno-fluorescence backgrounds with samples including serum, blood and non-targeted bacteria. The concentrated target cells are detected using fluorescently-labeled antibodies. With a single 2.0×2.0×0.3 mm PAM filter, as few as 10 rickettsial organisms per 100 µl of lysed blood sample can be analyzed within 60 min, as compared to hours or even days needed for conventional detection methods. This method is highly relevant to rapid, multiplexed, low-cost point of care diagnostics at early stages of infection where diagnostics providing more immediate and actionable test results are needed to improve patient outcomes and mitigate potential natural and non-natural outbreaks or epidemics of rickettsial diseases.
我们展示了微流控技术在快速检测复杂生物样本中少至 10 个立克次体生物方面的进展。在微流道内制作的免疫反应性过滤器——大孔聚丙烯酰胺整体柱(PAM)增强了固相免疫捕获、目标细菌的染色和检测。由于尺寸排阻,流过通道的样本中的细菌细胞被迫与 PAM 过滤器表面相互作用,克服了常见的传输和动力学限制,实现了快速(分钟级)、高效率(~100%)的捕获。在此过程中,10 μl 至 >100 μl 的样本体积中的目标细胞在微通道中的 PAM 过滤器边缘的亚 50 nl 区域内浓缩,从而浓缩了 1000 倍以上。这大大提高了灵敏度,因为亲水的 PAM 还可以产生低非特异性免疫荧光背景,包括血清、血液和非目标细菌。浓缩的目标细胞使用荧光标记的抗体进行检测。使用单个 2.0×2.0×0.3 mm 的 PAM 过滤器,在 60 分钟内即可分析 100 µl 裂解血样中少至 10 个立克次体生物,而传统检测方法则需要数小时甚至数天。这种方法与快速、多重、低成本的即时护理诊断高度相关,可在感染的早期阶段进行,此时需要提供更直接和可操作的检测结果的诊断方法,以改善患者的预后并减轻潜在的自然和非自然爆发或立克次体疾病的流行。