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Microfluidic detection of waterborne pathogen through light scattering of particle immunoassays.

机译:通过粒子免疫测定法的光散射对水性病原体进行微流检测。

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摘要

This dissertation focused on detecting waterborne pathogens in a microfluidic biosensing system which enables point-of-care, real-time monitoring. Within this framework, I have been addressing three objectives.;The first objective was to enhance mixing of particles in a microfluidic device. To this end, SDS (sodium dodecyl sulfate) or Tween 80 (polyethylene sorbitol ester) was added to the antibody-conjugated polystyrene microparticle suspension. Both surfactants showed non-specific binding (with SDS) or very poor diffusion (with Tween 80). As an alternative approach, highly carboxylated polystyrene microparticles showed very low non-specific binding comparable to that with Tween 80 and good diffusional mixing equivalent to that with SDS. This work was published in Appendix A (© 2008 Elsevier).;The second objective was to detect E. coli K-12 using the microfluidic-based system with low detection limit in Appendix B (© 2008 Elsevier). This method was essentially one-step and requires no sample pre-treatment or cell culturing. Conventional immunoassay using polyclonal antibody detects not only viable cells, but also dead cell and free antigens. In order to reduce false positive signal originated from dead cells and free antigens, target solution was washed three times. The detection limit was as low as 40 cfu ml-1 or 4 cfu per device (viable cells only), or <10 cfu ml-1 or <1 cfu per device (including dead cells and free antigens).;Our final objective was to develop real-time, high sensitive method for detecting waterborne pathogens in a water distribution system in Appendix C. Detection of Escherichia coli (E. coli) in a single straight pipe was demonstrated using a microfluidic 10 system utilizing light scattering detection of latex immunoagglutination assay. Assay time is <5 min per assay and detection limit is 10 cfu ml-1. Optical signals are compared with viable E. coli counts (not real time) and salt tracer experiments. Laminar (Re = 1,102) and turbulent (Re = 6,144) flows are used to simulate the flow regimes in a real water distribution system.
机译:本论文的重点是在微流控生物传感系统中检测水生病原体,该系统可实现即时的即时监测。在此框架内,我一直在解决三个目标。第一个目标是增强微流控设备中颗粒的混合。为此,将SDS(十二烷基硫酸钠)或Tween 80(聚乙烯山梨糖醇酯)加入抗体缀合的聚苯乙烯微粒悬浮液中。两种表面活性剂均表现出非特异性结合(与SDS结合)或极差的扩散(与Tween 80结合)。作为一种替代方法,高度羧基化的聚苯乙烯微粒表现出与Tween 80相当的非常低的非特异性结合,并具有与SDS相当的良好扩散混合。这项工作发表在附录A(©2008 Elsevier)中;第二个目标是使用附录B中具有低检出限的基于微流体的系统检测大肠杆菌K-12(©2008 Elsevier)。该方法实质上是一个步骤,不需要样品预处理或细胞培养。使用多克隆抗体的常规免疫测定不仅检测活细胞,而且检测死细胞和游离抗原。为了减少源自死细胞和游离抗原的假阳性信号,将目标溶液洗涤三遍。每个设备的检测限低至40 cfu ml-1或4 cfu(仅活细胞),或每个设备<10 cfu ml-1或<1 cfu(包括死细胞和游离抗原)。;我们的最终目标是以开发用于检测附录C中供水系统中水生病原体的实时,高灵敏度方法。使用微流控10系统,利用光散射检测乳胶免疫凝集法,证明了在单个直管中检测大肠杆菌(E. coli)。分析。每个分析的分析时间少于5分钟,检测限为10 cfu ml-1。将光信号与可行的大肠杆菌计数(不是实时)和盐示踪剂实验进行比较。层流(Re = 1,102)和湍流(Re = 6,144)被用来模拟真实配水系统中的流动状态。

著录项

  • 作者

    Han, Jin-Hee.;

  • 作者单位

    The University of Arizona.;

  • 授予单位 The University of Arizona.;
  • 学科 Engineering Agricultural.;Engineering Biomedical.;Engineering Environmental.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 99 p.
  • 总页数 99
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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