Center for Applied NanoBioscience & Medicine, College of Medicine - Phoenix, University of Arizona, Phoenix, AZ, USA.
Department of Microbiology and Immunology, University of Nevada School of Medicine, Reno, NV, USA.
Talanta. 2019 Jan 1;191:81-88. doi: 10.1016/j.talanta.2018.08.043. Epub 2018 Aug 17.
Currently, the standard method for identifying biological agents of potential threats to national security and public health, such as pathogens, virus, and toxins, mainly rely on microbiological cultivation. This method is time-consuming and it requires sophisticated equipment and well-trained personnel, which are often unavailable in remote areas or at point-of-need. Therefore, an alternative rapid, simple, and sensitive method for detecting bio-threat agents is in crucial need. We report a paper-based Vertical Flow Immunoassay (VFI) device that can overcome these limitations. The VFI device utilizes a nanoporous nitrocellulose membrane encapsulated in a stainless steel filter holder. As the sample is pushed through the membrane, which is pre-functionalized with capture antibody, a sandwich assay is formed and colorimetric signal is generated to reflect the presence of target antigens. Through theoretical analyses of antigen-antibody binding process inside a porous membrane, we identified two critical factors - membrane pore size and sample flow rate that can be optimized to improve the assay sensitivity. Then, the effects were demonstrated through experimental studies using Burkholderia pseudomallei (the causative agent of melioidosis) as a model pathogen. The B. pseudomallei VFI was based on an immunoassay targeting the B. pseudomallei surface capsular polysaccharide (CPS). The experimental results agreed well with the theory showing that increasing the flow speed (up to 1.06 mm/s) and reducing the membrane pore size (down to 0.1 µm) could improve the sensitivity by at least 5 times. The VFI's limit-of-detection for CPS spiked in buffer solution was determined to be 0.02 ng/mL. The developed VFI shows great potential as a point-of-care tool for detection of bio-threat agents in a variety of clinical and resource-restricted conditions.
目前,识别对国家安全和公众健康构成潜在威胁的生物制剂(如病原体、病毒和毒素)的标准方法主要依赖于微生物培养。这种方法耗时耗力,需要复杂的设备和经过良好培训的人员,而这些在偏远地区或现场往往无法获得。因此,迫切需要一种替代的快速、简单、灵敏的生物威胁剂检测方法。我们报告了一种基于纸的垂直流动免疫分析(VFI)装置,该装置可以克服这些限制。VFI 装置利用纳米多孔硝酸纤维素膜封装在不锈钢过滤器支架中。当样品通过预先用捕获抗体功能化的膜时,形成夹心测定法,并且产生比色信号以反映目标抗原的存在。通过对多孔膜内抗原-抗体结合过程的理论分析,我们确定了两个关键因素-膜孔径和样品流速,可以对其进行优化以提高测定的灵敏度。然后,通过使用伯克霍尔德氏菌(导致类鼻疽病的病原体)作为模型病原体的实验研究来证明这些效果。B. pseudomallei VFI 是基于针对 B. pseudomallei 表面荚膜多糖(CPS)的免疫测定法。实验结果与理论吻合良好,表明增加流速(高达 1.06mm/s)和减小膜孔径(降至 0.1μm)至少可以将灵敏度提高 5 倍。在缓冲溶液中加入 CPS 的 VFI 的检测限确定为 0.02ng/mL。开发的 VFI 具有作为在各种临床和资源受限条件下检测生物威胁剂的即时护理工具的巨大潜力。