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组织中光纤探头的照明和荧光收集体积

Illumination and fluorescence collection volumes for fiber optic probes in tissue.

作者信息

Tai Dean C S, Hooks Darren A, Harvey John D, Smaill Bruce H, Soeller Christian

机构信息

The University of Auckland, Bioengineering Institute and Department of Physics, Auckland, New Zealand 1001.

出版信息

J Biomed Opt. 2007 May-Jun;12(3):034033. doi: 10.1117/1.2750288.

Abstract

Optical fibers can deliver light to, and collect it from, regions deep in tissue. However, reported illumination and fluorescence collection volumes adjacent to the fiber tip have been inconsistent, and systematic data on this topic are not available. Illumination and fluorescence collection profiles were characterized with high spatial resolution for different optical fibers in tissue and various fluids using two-photon flash photolysis and excitation. We confirm that illumination and fluorescence collection volumes for optical fibers are near identical. Collection volume is determined by the core dimensions and numerical aperture (NA) of the fiber and the scattering properties of the medium. For a multimode optical fiber with 100 microm core diam and NA=0.22, 80% of the total fluorescence is collected from a depth of 170 microm in tissue and 465 microm in nonscattering fluid. A semiempirical mathematical description of photon flux adjacent to the fiber tip was also developed and validated. This was used to quantify the extent of temporal blurring associated with propagation of a wavefront of altered fluorescence emission across the region addressed by fiber optic probes. We provide information that will facilitate the design of optical probes for tissue imaging or therapeutic applications.

摘要

光纤能够将光传输至组织深处,并从这些区域收集光。然而,已报道的光纤尖端附近的照明和荧光收集体积并不一致,且关于该主题的系统数据也尚未可得。利用双光子闪光光解和激发技术,以高空间分辨率对不同光纤在组织和各种流体中的照明和荧光收集剖面进行了表征。我们证实,光纤的照明和荧光收集体积几乎相同。收集体积由光纤的纤芯尺寸、数值孔径(NA)以及介质的散射特性决定。对于纤芯直径为100微米、NA = 0.22的多模光纤,80%的总荧光是从组织中170微米的深度以及非散射流体中465微米的深度收集到的。还开发并验证了光纤尖端附近光子通量的半经验数学描述。这被用于量化与改变的荧光发射波前在光纤探针所覆盖区域传播相关的时间模糊程度。我们提供的信息将有助于设计用于组织成像或治疗应用的光学探针。

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