Carbon Nanotube Field Emission Microbeam Array for Single Cell Irradiation

用于单细胞辐照的碳纳米管场发射微束阵列

• 批准号: 7268041
• 负责人: SHA X CHANG
• 金额: $ 13.35万
• 依托单位: UNIV OF NORTH CAROLINA CHAPEL HILL
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-07-14 至 2009-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7268041
• 关键词: Applications Grants; Area; Astronauts; Biological Markers; Biology; Biomedical Engineering; Biosensor; Cancer Patient; Carbon; Cells; Cellular biology; Complex; DNA Damage; Depth; Development; Device Designs; Device or Instrument Development; Devices; Electrons; Emergency Situation; Epidermal Growth Factor Receptor; Event; Exposure to; Flowcharts; Funding; Future; Goals; Imaging Techniques; In Vitro; Individual; Interdisciplinary Study; Ionizing radiation; Knowledge; Laboratories; MEKKs; Malignant Neoplasms; Microscopic; Mission; Molecular; Molecular Target; Molecular and Cellular Biology; Nanotechnology; Pathway interactions; Physiologic pulse; Play; Pliability; Population; Power Sources; Property; Pulse taking; Purpose; Radiation; Radiation Protection; Radiation therapy; Radiation, Other; Radiation-Sensitizing Agents; Regulation; Relative (related person); Research; Research Personnel; Resources; Risk; Role; Safety; Signal Pathway; Solid; Talents; Technology; Terrorism; Testing; Time; TimeLine; Treatment Protocols; base; cancer therapy; cellular imaging; concept; design; experience; fight against; innovation; instrumentation; irradiation; new technology; novel; prevent; programs; prototype; repaired; research study; response; size; sound; stressor

DESCRIPTION (provided by applicant): Advancements in the fields of radiation therapy and radiation protection are hindered by our lack of a thorough understanding of molecular events that underlie the radiation response of cells. One reason is the shortage of specialized instrumentation required by such studies on very small time and spatial scales. The inability to deliver radiation on microscopic scale can be especially detrimental when the radiation response of one or a few cells needs to be distinguished from that of an entire cell population. Many believe that long term radiation sequelae-that may not manifest themselves for decades-are regulated by events in signaling pathways, DNA damage assessment and repair, all occurring within the first few minutes following irradiation. To provide the much needed new cellular irradiation technology we propose to develop nanotechnology based microbeam array devices that can deliver low LET electron irradiation to individual cells in vitro simultaneous with real-time microscopic observation. Based on the unique field emission property of carbon nanotube the device delivers radiation from its 10,000 individually controlled microbeam-producing pixels. Radiation delivery can be spatially discreet or uniform, continuous or pulsed at a less than microsecond time scale. Most important from a radiation safety standpoint, the microbeams cause negligible radiation exposure to the operator, thus the devices do not require special shielding. Once developed, the Petri-dish- sized microbeam devices can become available to many laboratories to study molecular targets for the development of new radiosensitizers and radioprotectors. Specifically, in this proposal we propose to 1) determine specifications for the microbeam devices for cellular research; 2) perform fabrication and commissioning of a prototype single pixel microbeam device; 3) demonstrate the feasibility of the microbeam device in specific in vitro experiments including analyzing spatio-temporal regulation of EGFR, Ras, and MEKK pathways; and 4) develop and fabricate a multi-pixel microbeam array device. Together with the use of new biomarkers and cellular imaging techniques, the proposed device promises to open up new research capabilities for the identification and manipulation of radiation responses - an understanding vital to improvements in cancer therapy, the protection of astronauts on deep-space missions, and the protection of emergency-responders and the public against radiological terrorism.

描述（由申请人提供）：放射治疗和放射防护领域的进展受到我们缺乏对细胞辐射反应基础的分子事件的透彻理解的阻碍。原因之一是缺乏在非常小的时间和空间尺度上进行这种研究所需的专门仪器。当一个或几个细胞的辐射反应需要与整个细胞群的辐射反应区分开来时，无法在微观尺度上提供辐射可能特别有害。许多人认为，长期辐射后遗症-可能几十年都不会表现出来-是由信号通路，DNA损伤评估和修复中的事件调节的，所有这些都发生在辐射后的最初几分钟内。为了提供急需的新的细胞照射技术，我们建议开发基于纳米技术的微束阵列设备，可以提供低LET电子照射到单个细胞在体外同时进行实时显微镜观察。基于碳纳米管独特的场致发射特性，该设备从其10，000个单独控制的微束产生像素提供辐射。辐射递送可以是空间离散的或均匀的、连续的或以小于微秒的时间尺度脉冲的。从辐射安全的角度来看，最重要的是，微束对操作者造成的辐射暴露可以忽略不计，因此设备不需要特殊的屏蔽。一旦开发出来，培养皿大小的微束装置就可以被许多实验室用来研究分子靶点，以开发新的辐射增敏剂和辐射防护剂。具体而言，在该提案中，我们建议1）确定用于细胞研究的微束设备的规格; 2）进行原型单像素微束设备的制造和调试; 3）在特定的体外实验中证明微束设备的可行性，包括分析EGFR，Ras和MEKK通路的时空调节;以及4）开发和制造多像素微束阵列设备。连同使用新的生物标志物和细胞成像技术，拟议的设备有望开辟新的研究能力，用于识别和操纵辐射反应-这对改善癌症治疗，保护深空任务中的宇航员以及保护应急人员和公众免受辐射恐怖主义的影响至关重要。