Modern clearing techniques for the three-dimensional (3D) visualisation of neural tissue microstructure have been very effective when used on rodent brain but very few studies have utilised them on human brain material, mainly due to the inherent difficulties in processing post-mortem tissue. Here we develop a tissue clearing solution, OPTIClear, optimised for fresh and archival human brain tissue, including formalin-fixed paraffin-embedded material. In light of practical challenges with immunostaining in tissue clearing, we adapt the use of cresyl violet for visualisation of neurons in cleared tissue, with the potential for 3D quantification in regions of interest. Furthermore, we use lipophilic tracers for tracing of neuronal processes in post-mortem tissue, enabling the study of the morphology of human dendritic spines in 3D. The development of these different strategies for human tissue clearing has wide applicability and, we hope, will provide a baseline for further technique development.
Applying Artmann's formula to a light beam in the TM state of wave polarization, we show analytically the existence of a large and negative Goos-Hänchen shift near the angle of the Brewster dip on reflection from a weakly absorbing semi-infinite medium. The shift is opposite that in the case of total internal reflection, and it can be an order of magnitude larger than a wavelength if the absorption of the reflecting medium is sufficiently weak. Examples are given, and the detectibility of the shift is discussed.
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