Brunette I, Nelson L R, Bourne W M
Department of Ophthalmology, Mayo Foundation, Rochester, Minnesota 55905.
Cryobiology. 1989 Dec;26(6):513-23. doi: 10.1016/0011-2240(89)90076-x.
As an initial step in the development of a method for corneal cryopreservation by vitrification, we attempted to establish the maximum concentration of glycerol to which human corneal endothelium could be exposed at 4 degrees C for 15 min without damage. Damage was defined as an increase in mean endothelial cell size or the inability to maintain corneal thickness for 1 week after exposure to glycerol. Using a system for long-term corneal perfusion, we perfused 24 paired human corneas with glycerol at 4 degrees C. The concentration of glycerol increased at a rate of 20% (w/v) (2.2 M) per hour until the desired maximum concentration was reached for that cornea, stabilized for 15 min, and then decreased at the same rate. The corneas were then perfused at 37 degrees C with Dulbecco's medium at a rate of 5 microliters/min under 18 mm Hg intracameral pressure for 7 days with daily measurements of corneal thickness. Endothelial morphology was examined by specular microscopy and by scanning electron microscopy. After 7 days of perfusion at 37 degrees C, there was a statistically significant direct relationship between the maximum concentration of glycerol to which the experimental eyes had been exposed and the increase in mean endothelial cell size. The mean endothelial cell size increased in corneas exposed to glycerol concentrations of 40, 50, and 60% (w/v), but did not differ significantly from baseline measurements in the corneas exposed to 30% glycerol or less. Thus, there was no detectable damage to human corneas exposed to 30% (w/v) (3.3 M) glycerol in this system. Tolerance of higher concentrations may be achieved by changes in the rates of addition and removal of glycerol or in the composition of the perfusate.
作为通过玻璃化法进行角膜冷冻保存方法开发的第一步,我们试图确定人角膜内皮细胞在4℃下暴露于甘油15分钟而不受损伤的最大浓度。损伤定义为平均内皮细胞大小增加,或在暴露于甘油后1周内无法维持角膜厚度。使用长期角膜灌注系统,我们在4℃下用甘油灌注24对人角膜。甘油浓度以每小时20%(w/v)(2.2M)的速率增加,直到达到该角膜所需的最大浓度,稳定15分钟,然后以相同速率降低。然后在37℃下,在18mmHg前房压力下,以5微升/分钟的速率用杜尔贝科培养基灌注角膜7天,并每天测量角膜厚度。通过镜面显微镜和扫描电子显微镜检查内皮形态。在37℃灌注7天后,实验眼暴露于甘油的最大浓度与平均内皮细胞大小的增加之间存在统计学上显著的直接关系。暴露于40%、50%和60%(w/v)甘油浓度的角膜中平均内皮细胞大小增加,但与暴露于30%或更低甘油浓度的角膜中的基线测量值相比,差异不显著。因此,在该系统中,暴露于30%(w/v)(3.3M)甘油的人角膜没有可检测到的损伤。通过改变甘油添加和去除的速率或灌注液的组成,可以实现对更高浓度的耐受性。