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SBIR Phase I: Fluidic Processor

SBIR Phase I: Fluidic Processor
SBIR 第一阶段:流体处理器
批准号:
1113588
负责人:
Neil Picha
金额:
$15.0万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-07-01 至 2011-12-31

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中文摘要
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英文摘要
This Small Business Innovation Research (SBIR) Phase I project will support the development of a fluidic processor capable of performing complex fluidic processes. In Phase I, we will demonstrate the utility of this device in two-dimensional liquid chromatography (2DLC), where existing valve technologies currently severely limit the performance of 2DLC. This project seeks to radically change the way fluids are moved, switched, processed, stored, and detected within a fluidics system. Current state-of-the-art fluid switching devices, such as rotary and solenoid valves, actuate in a single dimension thereby severely limiting the fluidic calculations and permutations that can be derived from single or even multiple concatenated devices. Furthermore, because they are one-dimensional devices, they have problems with analyte carry over, channel cross talk, and are generally design limited. This novel concept breaks down the traditional design barriers that constrain the implementation of current fluidics. To accomplish this, the concept transcends the single dimension and embraces two- and three-dimensional fluid processing in the context of a valve. The project will result in a random access, multi-dimensional, multi-purpose valve platform with specific application to metabolomics and proteomics separations. The broader impacts of this activity include application of the device to greatly expand research and analytical capabilities of instruments for 2-dimensional separations, food testing, drug discovery, GMO testing, and other critical analytical and bioprocessing applications. The device addresses the most vexing problem of interfacing of micro and macro fluidics and enables massively parallel manipulation of fluids. The project also will train and provide research experience for undergraduates. If successful, this project will contribute and enable new frontiers of systems biology research aimed at driving greater knowledge of biochemical interactions, mechanisms and biomarker discovery.
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