In vivo microendoscopy for imaging deep regions of the brain
In vivo microendoscopy for imaging deep regions of the brain
批准号:
G0701061/1
负责人:
N Emptage
金额:
$39.65万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2008
资助国家:
英国
项目状态:
已结题
起止时间:
2008 至 --
中文摘要
对哺乳动物大脑深处的单个细胞进行成像的能力将为基础和临床科学开辟新的研究机会。目前的脑成像技术不能提供组织的高分辨率图像。例如,诸如磁共振成像(MRI)的大脑扫描技术仅实现几毫米的分辨率。在这样一个区域内,可能有几千个细胞,每个细胞执行一项独特的任务。虽然现代光学显微镜可以达到观察单个细胞所需的分辨率,但它们只能看到直接放置在显微镜透镜前面的物体。回想一下,在生物课上,在显微镜载玻片上找到细胞是多么令人沮丧!要创建一种能够在大脑深处成像的方法,也可以观察单细胞的活动,将需要一种新的光学设备。互联网的繁荣不仅为我们的指尖带来了巨大的信息财富,而且推动了电信行业在微光学领域取得了重大发展。梯度折射率(GRIN)透镜,其中光被引导作为光学介质中的内部变化的结果,现在生产成本低,并具有亚毫米尺寸。目前最小的GRIN透镜的直径只有头发丝的直径,大约100微米。与传统透镜不同,GRIN透镜不是研磨成形的,而是通过掺杂玻璃制成的,然后可以挤出到所需的直径。有点像介绍海滨摇滚的方法。由于其微小的尺寸,GRIN透镜可用于生产微型内窥镜。基于GRIN透镜的内窥镜将像传统内窥镜一样能够实现对身体的远程部分的进入,然而,GRIN透镜内窥镜由于如此小而将是微创的。因此,通过结合这些设备的关键特性,将有可能对大脑中以前无法访问的部分中的单个细胞进行成像。
英文摘要
The ability to image individual cells deep within the mammalian brain will open new research opportunities in both basic and clinical science. Current brain imaging techniques do not provide high-resolution images of the tissues. For example, brain scanning techniques such as magnetic resonance imaging (MRI) only achieve a resolution of a few millimeters. Within such an area there may be several thousand cells, each performing a unique task. Although modern light microscopes can achieve the resolution needed to see individual cells they can only visualize objects placed immediately in front of the microscope lens. Recall how frustrating it was in biology class to find the cells on the microscope slide! To create a method capable of imaging deep within the brain, that can also observe what single cells are doing, will require a new optical device. The internet boom has not only brought an enormous wealth of information to our fingertips but has driven the telecommunications industry to achieve significant developments in the area of micro-optics. Gradient refractive index (GRIN) lenses, in which light is guided as a consequence of the internal variations in optical medium, are now produced cheaply and with sub-millimeter dimensions. Currently the smallest GRIN lenses have the diameter of a human hair, around100 microns. Unlike traditional lenses, GRIN lenses are not ground to shape but generated by doping glass that can then be extruded to the desired diameter. A little like the method used to introduce the letters to seaside rock. Due to their tiny dimensions, GRIN lenses can be used to produce miniature endoscopes. GRIN lens based endoscopes will, like a traditional endoscope be able to achieve access to remote parts of the body, however , a GRIN lens endoscope will be minimally invasive as a consequence of being so small. Thus by combining key characteristics of these devices it will be possible to image individual cells within previously inaccessible parts of the brain.
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