高光谱成像
显微镜
光学
双光子激发显微术
光谱成像
体内
临床前影像学
烟酰胺腺嘌呤二核苷酸
荧光
光子计数
材料科学
荧光显微镜
核磁共振
生物物理学
光子
物理
生物
计算机科学
生物技术
人工智能
NAD+激酶
酶
作者
Andrew J. Radosevich,Matthew B. Bouchard,Sean A. Burgess,Brenda R. Chen,Elizabeth M. C. Hillman
出处
期刊:Optics Letters
[The Optical Society]
日期:2008-09-12
卷期号:33 (18): 2164-2164
被引量:68
摘要
In vivo two-photon imaging of intrinsic contrast can provide valuable information about structural tissue elements such as collagen and elastin and fluorescent metabolites such as nicotinamide adenine dinucleotide. Yet low signal and overlapping emission spectra can make it difficult to identify and delineate these species in vivo. We present a novel approach that combines excitation scanning with spectrally resolved emission two-photon microscopy, allowing distinct structures to be delineated based on their characteristic spectral fingerprints. The amounts of intrinsic fluorophores present in each voxel can also be evaluated. We demonstrate our method using in vivo imaging of nude mouse skin.
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