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penetration depth limits of in vivo confocal reflectance imaging

机译:共聚焦反射成像的穿透深度极限

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摘要

We present experiments to predict the maximum penetration depth at which typical biological structures in amelanotic tissue can be detected with confocal microscopy. The detected signal is examined as the signal source strength (index of refraction mismatch), the source depth, and the medium scattering coefficient are varied. The detected background produced by scattering outside the focal volume is examined as the medium scattering coefficient, the depth in the medium, the dimensionless pinhole radius, v↓(p), and the shape of the scattering phase function are varied. When the system approaches ideal confocal performance (v↓(p) #3 )t,he penetration depth is limited by the signal-to-noise ratio to approximately 3-4 optical depths (OD's) for a 0.05 index mismatch. As v↓(p)increases to 8, the penetration depth is limited by the signal-to-background ratio and is dependent on the scattering coefficient. Atμ↓(s)= 100 cm↑(-1) (↓(s) = 100μm) and an index mismatch of 0.05, the maximum penetration depth is approximately 2 OD. #1998 Optical Society of America OCIS codes: 110.0110, 120.5700, 290.0290.
机译:我们目前的实验,以预测最大的穿透深度,在该深度可以通过共聚焦显微镜检测到搪瓷组织中的典型生物结构。随着信号源强度(折射率失配),源深度和介质散射系数的变化,检查检测到的信号。将检测到的由焦点体积之外的散射产生的背景作为介质散射系数,介质中的深度,无量纲的针孔半径,v↓(p)和散射相位函数的形状进行了更改。当系统达到理想的共焦性能(v↓(p)#3)t时,对于0.05的折射率失配,穿透深度受信噪比的限制,约为3-4个光学深度(OD)。当v↓(p)增加到8时,穿透深度受到信噪比的限制,并且取决于散射系数。在μ↓= 100 cm↑(-1)(↓=100μm)且折射率不匹配为0.05时,最大穿透深度约为2 OD。 #1998美国光学学会OCIS代码:110.0110、120.5700、290.0290。

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