Smithpeter C L, Dunn A K, Welch A J, Richards-Kortum R
Appl Opt. 1998 May 1;37(13):2749-54. doi: 10.1364/ao.37.002749.
We present experiments to predict the maximum penetration depth atwhich typical biological structures in amelanotic tissue can bedetected with confocal microscopy. The detected signal is examinedas the signal source strength (index of refraction mismatch), thesource depth, and the medium scattering coefficient are varied. Thedetected background produced by scattering outside the focal volume isexamined as the medium scattering coefficient, the depth in the medium, the dimensionless pinhole radius, nu(p), and theshape of the scattering phase function are varied. When the systemapproaches ideal confocal performance (nu(p) ? 3), the penetration depth is limited by the signal-to-noiseratio to approximately 3-4 optical depths (OD's) for a 0.05 indexmismatch. As nu(p) increases to 8, thepenetration depth is limited by the signal-to-background ratio and isdependent on the scattering coefficient. At mu(s) = 100 cm(-1) (l(s) = 100 mum) and an index mismatch of 0.05, the maximum penetrationdepth is approximately 2 OD.
我们开展了一些实验,以预测在共聚焦显微镜下能够检测到无黑色素组织中典型生物结构的最大穿透深度。当信号源强度(折射率失配)、源深度和介质散射系数发生变化时,对检测到的信号进行了研究。当介质散射系数、介质中的深度、无量纲针孔半径ν(p)以及散射相位函数的形状发生变化时,对焦点体积外散射产生的检测背景进行了研究。当系统接近理想共聚焦性能(ν(p) ?3)时,对于0.05的折射率失配,穿透深度受信噪比限制,约为3 - 4个光学深度(OD)。随着ν(p)增加到8,穿透深度受信号与背景比限制,并且取决于散射系数。在μ(s) = 100 cm(-1)(l(s) = 100 μm)且折射率失配为0.05时,最大穿透深度约为2个OD。