首页> 外文期刊>Microscopy and microanalysis: The official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada >Multi-photon Excitation Microscopy and Confocal Microscopy Imaging of In Vivo Human Skin: A Comparison
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Multi-photon Excitation Microscopy and Confocal Microscopy Imaging of In Vivo Human Skin: A Comparison

机译:体内人皮肤的多光子激发显微镜和共聚焦显微镜成像:比较

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摘要

We compare here multi-photon excitation microscopy and tandem scanning reflected light confocal microscopy for the microscopic observation of human skin in vivo. Multi-photon excitation is induced by a 80-MHz pulse train of femtosecond laser pulses at 780 nm wavelength. This nonlinear microscopic technique is inherently suitable for tissue fluorescence imaging because of its deeper penetration depth and lower specimen photodamage. This technique has noninvasively obtained tissue structural information in human epidermis and dermis. Alternatively, tandem scanning confocal light microscopy based on a white light source can provide video-rat image acquisition with high resolution and high contrast. Reflected light confocal methods have been used to obtain images from the skin surface to the epidermal-dermal junction. The relative merits of these two techniques can be identified by comparing three-dimensionally resolved images obtained from the forearm skin of the same volunteer.
机译:我们在这里比较多光子激发显微镜和串联扫描反射光共聚焦显微镜对人体皮肤在体内的显微观察。多光子激发是由波长为780 nm的飞秒激光脉冲的80 MHz脉冲序列引起的。这种非线性显微镜技术固有的适用于组织荧光成像,因为它具有更深的穿透深度和更低的样品光损伤。该技术具有非侵入性地获得了人表皮和真皮中的组织结构信息。替代地,基于白光源的串联扫描共聚焦显微镜可以提供具有高分辨率和高对比度的视频大鼠图像采集。反射光共聚焦方法已经用于获得从皮肤表面到表皮-真皮接合处的图像。通过比较从同一志愿者的前臂皮肤获得的三维分辨图像,可以确定这两种技术的相对优点。

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