Fong L P, Hunt C J, Taylor M J, Pegg D E
Br J Ophthalmol. 1986 Oct;70(10):751-60. doi: 10.1136/bjo.70.10.751.
Rabbit corneas were frozen and thawed by three methods and compared by full thickness transplantation as well as specular microscopy, histology, and transmission electron microscopy. Two of the methods used a recently described technique, in which the excised cornea was immersed in a potassium-rich buffered solution containing the cryoprotectant dimethyl sulphoxide (Me2SO, 2 mol/l). This solution was designed to restrict the loss of intracellular potassium and to prevent cell swelling at low temperatures. In one group the corneas were frozen and thawed surrounded by 5 ml of medium, while in the second group corneas were drained of excess fluid and frozen in air. The third group consisted of corneas cryopreserved by Capella and colleagues' method. All the cryopreserved corneas were damaged, but those that had been frozen in air after exposure to the new medium showed better structure and function than corneas frozen by either of the other two techniques.
采用三种方法对兔角膜进行冷冻和解冻,并通过全层移植以及镜面显微镜检查、组织学和透射电子显微镜检查进行比较。其中两种方法采用了一种最近描述的技术,即将切除的角膜浸入含有冷冻保护剂二甲基亚砜(Me2SO,2 mol/l)的富含钾的缓冲溶液中。该溶液旨在限制细胞内钾的流失,并防止低温下细胞肿胀。一组角膜在5毫升培养基包围下进行冷冻和解冻,而第二组角膜则排尽多余液体并在空气中冷冻。第三组由采用卡佩拉及其同事方法冷冻保存的角膜组成。所有冷冻保存的角膜均有损伤,但暴露于新培养基后在空气中冷冻的角膜比采用其他两种技术冷冻的角膜显示出更好的结构和功能。