Burns W A, Bretschneider A M, Morrison A B
Arch Pathol Lab Med. 1979 Apr;103(4):177-9.
Specimens destined for light and electron microscopy were fixed in a modified buffered formalin, postosmicated, dehydrated, and embedded in a mixture of epoxy resins (Epon-araldite) in large plastic molds. These blocks were sectioned at 0.5 to 1 micron on a JB-4 microtome and stained with a combined nuclear and cytoplasmic stain (Paragon). The sections were examined by light microscopy for diagnostic evaluation. If ultrastructural examination was also desired, the selected area was isolated using the "mesa" technique. The trimmed block was then sectioned on an ultramicrotome, picked up on grids, stained, and examined in the electron microscope. We think these techniques offer the diagnostic pathologist the potential of viewing 1-micron sections at a light microscopy level with the option of subsequent electron microscopy of the same area of the same block.
用于光学显微镜和电子显微镜检查的标本,先用改良的缓冲福尔马林固定,再进行后锇酸处理、脱水,然后嵌入大型塑料模具中的环氧树脂混合物(Epon-阿拉尔代特)中。将这些包埋块在JB-4切片机上切成0.5至1微米厚的切片,并用一种细胞核和细胞质联合染色剂(Paragon)染色。通过光学显微镜检查切片以进行诊断评估。如果还需要进行超微结构检查,则使用“台面”技术分离选定区域。然后将修整后的包埋块在超薄切片机上切片,放在载网上,染色,并在电子显微镜下检查。我们认为这些技术为诊断病理学家提供了在光学显微镜水平观察1微米切片的潜力,同时还可以选择对同一块组织的同一区域进行后续的电子显微镜检查。