Assessment of performance and safety of Corneal Chamber hypothermic storage medium and PSS-L corneal rinsing solution in human and porcine corneas.

IF 2 Q2 OPHTHALMOLOGY
Laura Giurgola, Umberto Rodella, Claudio Gatto, Orietta Rossi, Claudia Honisch, Eugenio Ragazzi, Paolo Ruzza, Stefano Ferrari, Jana D'Amato Tóthová
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Abstract

Purpose: To prove the safety and performance of the hypothermic corneal storage medium "Corneal Chamber" and the rinsing solution "PSS-L" in support of the new Conformité Européenne (CE) certification process in accordance with the Medical Device Regulation.

Methods: Fifteen (n=15) human donor corneas and 11 (n=11) porcine corneas were evaluated for the following parameters: endothelial cell density (ECD) and mortality, percentage of hexagonal cells (HEX%), coefficient of cellular area variation (CV%) and corneal transparency at Day 0 and after 14±1 days of storage in Corneal Chamber medium at 2-8°C. Then, the same parameters were assessed after rinsing of corneas in PSS-L for 1 min at room temperature. Evaluation of gentamicin sulfate carryover after corneal storage and PSS-L rinsing was performed by ultra-high performance liquid chromatography analysis on human corneas homogenates.

Results: Human and porcine corneas stored in Corneal Chamber medium showed a good overall quality of the tissue according to the quality parameters evaluated. In particular, mean ECD, HEX% and CV% did not show statistically significant changes at the end of storage and endothelial mortality increased to 3.1±3.3 and 7.8±3.5% in human and porcine corneas, respectively. Tissue rinsing with PSS-L did not affect the quality parameters evaluated before and gentamicin sulfate residues were absent in human corneas.

Conclusions: Corneal preservation in Corneal Chamber medium at 2-8°C for 14 days and the corneal rinse with PSS-L are safe and effective procedures allowing the preservation of the corneal quality parameters as well as the complete elimination of gentamicin sulfate from the tissues before transplantation.Cite Now.

评估角膜室低温储存介质和 PSS-L 角膜冲洗液在人和猪角膜中的性能和安全性。
目的:证明低温角膜储存介质 "Corneal Chamber "和冲洗液 "PSS-L "的安全性和性能,以支持新的符合欧洲标准(CE)认证程序,符合医疗器械法规:对 15 (n=15) 个人类供体角膜和 11 (n=11) 个猪角膜进行了以下参数评估:第 0 天和在角膜室培养基(2-8°C)中保存 14±1 天后的内皮细胞密度 (ECD) 和死亡率、六角形细胞百分比 (HEX%)、细胞面积变化系数 (CV%) 和角膜透明度。然后,在室温下用 PSS-L 冲洗角膜 1 分钟后,评估相同的参数。通过对人类角膜匀浆进行超高效液相色谱分析,评估角膜储存和 PSS-L 冲洗后硫酸庆大霉素的携带情况:结果:根据所评估的质量参数,在角膜室培养基中储存的人和猪角膜组织总体质量良好。特别是,平均 ECD、HEX% 和 CV% 在贮存结束时未出现统计学意义上的显著变化,而人和猪角膜的内皮死亡率分别增至 3.1±3.3% 和 7.8±3.5%。用 PSS-L 冲洗组织不会影响之前评估的质量参数,人角膜中没有硫酸庆大霉素残留:在角膜室培养基(2-8°C)中保存角膜 14 天并用 PSS-L 冲洗角膜是安全有效的方法,不仅能保存角膜质量参数,还能在移植前完全清除组织中的硫酸庆大霉素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMJ Open Ophthalmology
BMJ Open Ophthalmology OPHTHALMOLOGY-
CiteScore
3.40
自引率
4.20%
发文量
104
审稿时长
20 weeks
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