课题基金 / 基金详情

DNA Analysis in Multi-Phase Microfabricated Devices

DNA Analysis in Multi-Phase Microfabricated Devices
多相微加工器件中的 DNA 分析
批准号:
7901447
负责人:
Mark A BURNS
金额:
$32.39万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-08-01 至 2012-07-31

项目摘要

项目成果

Mark A BURNS的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Infectious diseases represent a significant healthcare cost burden. For bacterial infections, especially chronic ones, antibiotics are selected for treatment not knowing whether the drugs selected are appropriate for the infecting pathogen. Although viral infections have few effective treatments, patients desire medication before they leave their primary care physician's office. Antibiotics are often prescribed for viral infections because the patient demands them not realizing they are ineffective, or the physician provides them as a precautionary measure. Clearly, rapidly and accurately identifying infectious pathogens will lead to fewer unnecessary prescriptions, reduced hospitalization time, and a reduction in the spread of antibiotic resistant microbes. We propose to develop a genetic analysis microfluidic system that uses a single pneumatic input for fluidic control, and a multiplexed reaction system for species identification. The device will use a series of reaction chambers followed by a separation channel to determine the class of infecting agents and their specific resistance to antibiotics. We will target pathogens associated with acute (the common cold) and chronic (multiple-species bacterial) respiratory infections for our main applications. We choose these target areas for several reasons. First, for our strategy of small device size, we need a sample with sufficient pathogenic load to complete an analysis patient material from a swab, sputum, or nasal wash for these diseases typically has high pathogen numbers. Second, understanding the different pathogen species and strains and their infection time course could lead to better treatment and lower the use of antibiotics. Finally, the device can easily be extended to other viruses, bacterial agents, or genomic analysis with merely a change in the reagents.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
DOI: 10.3390/bios4010076
发表时间: 2014-03
期刊: Biosensors
影响因子: --
作者: [Li Y, Burke DT, Kopelman R, Burns MA]
通讯作者: Burns MA
DNA Analysis in Multi-Phase Microfabricated Devices
DNA Analysis in Multi-Phase Microfabricated Devices
Microfluidics in Biomedical Sciences Training Program
Microfluidics in Biomedical Sciences Training Program
海外基金