MICROFABRICATION FOR SORTING LARGE PARTICLES

用于分选大颗粒的微加工

• 批准号: 8361777
• 负责人: STEVEN W GRAVES
• 金额: $ 1.12万
• 依托单位: LOS ALAMOS NAT SECTY-LOS ALAMOS NAT LAB
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-04-01 至 2013-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8361777
• 关键词: Caliber; Collaborations; Development; Devices; Dimensions; Flow Cytometry; Fluorescence; Funding; Grant; Microfabrication; Microfluidics; National Center for Research Resources; Principal Investigator; Research; Research Infrastructure; Resources; Sampling; Sorting - Cell Movement; Source; Techniques; Technology; United States National Institutes of Health; Universities; cost; operation; particle; research and development; success

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. This collaboration with Dr. Mehmet Toner of the BioMEMS Center at Harvard University (a P41 Resource) is focused on applying microfabrication techniques to the development of a high-throughput large particle sorter in R&D Project 2. We are investigating passive particle manipulation within microfluidic channels. Using a variety of specific channel orientations, the BioMEMS Center has been able to show particle focusing, periodic particle spacing, and parallel streamlines with no external fields. We are investigating the use of this technology to focus particles in the 100-micron diameter range. We expect this approach to easily scale to this dimension and fabrication of multiple focusing channels on a single substrate should be straight- forward. As such we have obtained a few sample chips and analyzed focused particles in a simple fluorescence analysis device, with some success. The advantages of this approach include robustness, reproducible operation and no need for any external particle manipulation field.

这个子项目是利用资源的许多研究子项目之一。 由NIH/NCRR资助的中心拨款提供。对子项目的主要支持 子项目的首席调查员可能是由其他来源提供的， 包括美国国立卫生研究院的其他来源。为子项目列出的总成本可能 表示该子项目使用的中心基础设施的估计数量， 不是由NCRR赠款提供给次级项目或次级项目工作人员的直接资金。 这项与哈佛大学生物MEMS中心的Mehmet Toner博士的合作(P41资源)专注于将微制造技术应用于研发项目2中的高通量大颗粒分选器的开发。我们正在研究微流控通道中的被动颗粒操纵。使用各种特定的通道方向，BioMEMS中心已经能够在没有外场的情况下显示粒子聚焦、周期性粒子间距和平行流线。我们正在研究使用这项技术来聚焦直径在100微米范围内的颗粒。我们希望这种方法可以很容易地扩展到这个维度，并且在单个衬底上制造多个聚焦通道应该是直接的。因此，我们已经获得了几个样品芯片，并在一个简单的荧光分析设备上分析了聚焦的颗粒，取得了一定的成功。该方法具有稳健性好、操作重复性好、不需要任何外部粒子操纵场等优点。