Fong L P, Hunt C J, Pegg D E
Curr Eye Res. 1987 Apr;6(4):569-77. doi: 10.3109/02713688709025215.
There have been considerable difficulties in developing a satisfactory method for the cryopreservation of corneas. In this paper we describe the effect of two variables that appear to influence the effectiveness of preservation, the concentration of cryoprotectant and the medium that surrounds the cornea during freezing. Rabbit corneas were exposed to the cryoprotectant dimethyl sulphoxide (Me2SO) in concentrations of 1 or 2 mol/l in a high-potassium well-buffered solution, and then cooled to -196 degrees C either in air or surrounded by 5 ml of the Me2SO solution. After storage at -196 degrees C, thawing and removal of the Me2SO, survival was assessed by electron microscopy and measurement of stromal thickness during perfusion on the specular microscope. The least degree of damage was observed when corneas were equilibrated with 1M Me2SO and frozen in air. The evidence suggests that 2M may be an excessive concentration of Me2SO in this system and that damage to the stroma may be reduced by freezing the cornea in air rather than surrounded by the Me2SO solution.
在开发一种令人满意的角膜冷冻保存方法方面存在相当大的困难。在本文中,我们描述了两个似乎会影响保存效果的变量的作用,即冷冻保护剂的浓度以及冷冻过程中角膜周围的介质。将兔角膜置于高钾缓冲良好的溶液中,使其暴露于浓度为1或2摩尔/升的冷冻保护剂二甲基亚砜(Me2SO)中,然后在空气中或将其置于5毫升Me2SO溶液中冷却至 -196摄氏度。在 -196摄氏度下储存、解冻并去除Me2SO后,通过电子显微镜以及在镜面显微镜下灌注过程中测量基质厚度来评估角膜的存活情况。当角膜用1M Me2SO平衡并在空气中冷冻时,观察到的损伤程度最小。有证据表明,在该系统中2M的Me2SO浓度可能过高,并且通过在空气中冷冻角膜而非将其置于Me2SO溶液中,可减少对基质的损伤。