Weigum Shannon E, Xiang Lichen, Osta Erica, Li Linying, López Gabriel P
Materials Science, Engineering, and Commercialization Program, Texas State University, San Marcos, TX 78666, USA; Department of Biology, Texas State University, San Marcos, TX 78666, USA.
Materials Science, Engineering, and Commercialization Program, Texas State University, San Marcos, TX 78666, USA.
J Chromatogr A. 2016 Sep 30;1466:29-36. doi: 10.1016/j.chroma.2016.09.002. Epub 2016 Sep 4.
Separation of cells and microorganisms from complex biological mixtures is a critical first step in many analytical applications ranging from clinical diagnostics to environmental monitoring for food and waterborne contaminants. Yet, existing techniques for cell separation are plagued by high reagent and/or instrumentation costs that limit their use in many remote or resource-poor settings, such as field clinics or developing countries. We developed an innovative approach to isolate infectious pathogens from biological fluids using buoyant hollow silica microspheres that function as "molecular buoys" for affinity-based target capture and separation by floatation. In this process, antibody functionalized glass microspheres are mixed with a complex biological sample, such as stool. When mixing is stopped, the target-bound, low-density microspheres float to the air/liquid surface, which simultaneously isolates and concentrates the target analytes from the sample matrix. The microspheres are highly tunable in terms of size, density, and surface functionality for targeting diverse analytes with separation times of ≤2min in viscous solutions. We have applied the molecular buoy technique for isolation of a protozoan parasite that causes diarrheal illness, Cryptosporidium, directly from stool with separation efficiencies over 90% and low non-specific binding. This low-cost method for phenotypic cell/pathogen separation from complex mixtures is expected to have widespread use in clinical diagnostics as well as basic research.
从复杂生物混合物中分离细胞和微生物是许多分析应用中的关键第一步,这些应用涵盖从临床诊断到环境监测以检测食品和水源性污染物等领域。然而,现有的细胞分离技术存在试剂和/或仪器成本高昂的问题,这限制了它们在许多偏远或资源匮乏地区的使用,例如现场诊所或发展中国家。我们开发了一种创新方法,使用浮力中空二氧化硅微球从生物流体中分离感染性病原体,这些微球作为“分子浮标”,用于基于亲和力的目标捕获和通过浮选进行分离。在此过程中,抗体功能化的玻璃微球与复杂生物样品(如粪便)混合。当混合停止时,与目标结合的低密度微球漂浮到气/液表面,这同时从样品基质中分离并浓缩目标分析物。这些微球在尺寸、密度和表面功能方面具有高度可调性,可针对不同分析物,在粘性溶液中的分离时间≤2分钟。我们已将分子浮标技术应用于直接从粪便中分离导致腹泻疾病的原生动物寄生虫隐孢子虫,分离效率超过90%且非特异性结合低。这种从复杂混合物中进行表型细胞/病原体分离的低成本方法有望在临床诊断以及基础研究中得到广泛应用。