Sargent J A
Hexland Electron Microscopy Division, Oxford Instruments Limited, Eynsham, U.K.
Scanning Microsc. 1988 Jun;2(2):835-49.
Cryo-preparation of specimens for scanning electron microscopy can be completed within a few minutes. Chemical fixation and contact with solvents is avoided, levels of specimen hydration are maintained, low melting-point materials are stabilized, volume changes are minimized and internal structure can be revealed by freeze-fracture. Elements are not lost or substantially relocated prior to X-ray microanalysis and specimen luminescence is enhanced. The displacement of internal structure and material subject to X-ray microanalysis by the growth of ice crystals in hydrated samples can be minimized by adopting fast freezing methods designed to limit ice crystal growth. The technique enables a wide range of industrial and biological materials to be examined rapidly and free from artifacts commonly associated with more conventional preparation methods.
用于扫描电子显微镜的标本冷冻制备可在几分钟内完成。避免了化学固定和与溶剂的接触,保持了标本的水合水平,稳定了低熔点材料,使体积变化最小化,并且可以通过冷冻断裂揭示内部结构。在进行X射线微分析之前,元素不会丢失或大量重新分布,并且标本的发光得到增强。通过采用旨在限制冰晶生长的快速冷冻方法,可以将水合样品中冰晶生长导致的内部结构和受X射线微分析的材料位移降至最低。该技术能够快速检查各种工业和生物材料,且不会产生与更传统制备方法通常相关的伪像。