Hartmann C, Kolb M, Knauer I
Klin Monbl Augenheilkd. 1986 Apr;188(4):302-6. doi: 10.1055/s-2008-1050635.
A sequential corneal endothelium staining technique with trypan blue (TB)--alizarin red S (ARS)--ethanol-trypan blue is described which can be performed in a few minutes. The first step permits the TB exclusion to be determined as a criterion of normal endothelial cell function. The two following steps permit intercellular staining by ARS and nuclear staining by TB. After each staining procedure, fixation can be performed by methanol or ethanol, both with full-thickness corneal preparations or endothelial flat mounts. In flat preparations, the focussing problems and optical artifacts of full-thickness mounts can be avoided. These modifications render simple sequential staining with subsequent fixation a complement and alternative to specular microscopy and to the customary complicated silver staining of corneal endothelium.
描述了一种使用台盼蓝(TB)-茜素红S(ARS)-乙醇-台盼蓝的连续角膜内皮染色技术,该技术可在几分钟内完成。第一步可确定台盼蓝排斥作为正常内皮细胞功能的标准。接下来的两步可实现ARS的细胞间染色和TB的细胞核染色。每次染色后,可使用甲醇或乙醇进行固定,全层角膜标本或内皮平铺片均可。在内皮平铺片中,可避免全层标本的聚焦问题和光学假象。这些改进使后续固定的简单连续染色成为镜面显微镜检查和传统复杂角膜内皮银染色的补充和替代方法。