In vivo fluorescence imaging with high-resolution microlenses

被引:199
|
作者
Barretto, Robert P. J. [1 ]
Messerschmidt, Bernhard [2 ]
Schnitzer, Mark J. [1 ,3 ]
机构
[1] Stanford Univ, James H Clark Ctr Biomed Engn & Sci, Stanford, CA 94305 USA
[2] GRINTECH GmbH, Jena, Germany
[3] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
MICROOPTIC LENSES; ION-EXCHANGE; HIGH-SPEED; MICROENDOSCOPY; MICROSCOPY; MICE;
D O I
10.1038/nmeth.1339
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Micro-optics are increasingly used for minimally invasive in vivo imaging, in miniaturized microscopes and in lab-on-a-chip devices. Owing to optical aberrations and lower numerical apertures, a main class of microlens, gradient refractive index lenses, has not achieved resolution comparable to conventional microscopy. Here we describe high-resolution microlenses, and illustrate two-photon imaging of dendritic spines on hippocampal neurons and dual-color nonlinear optical imaging of neuromuscular junctions in live mice.
引用
收藏
页码:511 / U61
页数:4
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