Safety of a novel dual-chamber vial for corneal preservation

IF 2.7 2区 医学 Q1 OPHTHALMOLOGY
Joana Karanxha , Jack Cipolla , Diego A. Ojeda , Sarp Orgul , Katrina N. Llanes , Angela Gomez , William Buras , Elizabeth Fout , Charissa H. Tan , Sander R. Dubovy , Alfonso L. Sabater
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Abstract

Our group developed a novel dual-chamber corneal storage vial (DCV) comprised of two compartments that become isolated by the corneal button and prevent epithelial and endothelial interaction. We hypothesize that the DCV results in similar levels of corneal swelling and corneal endothelial cell (EC) death compared to the standard vial (SCV) and is safe for corneal storage.
To assess corneal thickness and EC density, human cornea pairs (N = 18) were recovered by the Florida Lions Eye Bank, with one cornea from each pair stored in the SCV and the other in the DCV. All cornea pairs were preserved in Optisol-GS media and stored at 2–8 °C for 2 weeks. Corneal thickness and EC density were evaluated on days 1, 7, and 14. Annexin V levels were measured in the corneal tissue (N = 12) to assess for cytotoxicity and apoptosis on day 14. Histological evaluation was performed on 3 additional cornea pairs on day 14. Three additional cornea pairs were collected to assess markers of endothelial cell death (casp3 and BID; N = 3) and endothelial cell function (ATP1A1, AQP1, and SLC4A4) were measured using RT-qPCR on 7 days (N = 3 for ATP1A1, AQP1 and N = 2 for SLC4A4).
Preliminary results revealed no significant differences in central corneal thickness at all time points between corneal button stored in the SCV compared to the DCV (p = 0.648, p = 0.295, p = 0.180). There was no significant difference in EC density between chambers at all time points (p = 0.451, p = 0.573, p = 0.666). After 14 days of storage in the DCV and SCV, histopathology slides demonstrated no difference in stromal swelling or endothelial cell loss upon examination under light microscopy. No differences were found in markers of endothelial cell death and function.
Given that the DCV demonstrates no difference in central corneal thickness, endothelial cell loss, or stromal swelling on histopathological examination during a two-week period, the DCV is a safe and viable alternative for corneal button storage. The DCV provides an alternative platform for human corneal storage for transplantation and allows the use of customized media in each compartment. The DCV can serve as a platform for future ex-vivo research, including the exploration and development of customized preservation solutions, such as the selective use of anti-fungal additives and other targeted interventions.
一种用于角膜保存的新型双腔小瓶的安全性。
我们的研究小组开发了一种新型的双室角膜储存瓶(DCV),由两个隔间组成,由角膜按钮隔离,防止上皮和内皮细胞相互作用。我们假设,与标准瓶(SCV)相比,DCV导致相似水平的角膜肿胀和角膜内皮细胞(EC)死亡,并且用于角膜储存是安全的。为了评估角膜厚度和EC密度,佛罗里达狮子眼库回收了人类角膜对(N=18),每对角膜中一个保存在SCV中,另一个保存在DCV中。所有角膜对在Optisol-GS培养基中保存,2-8℃保存2周。在第1、7、14天评估角膜厚度和EC密度。测定角膜组织(N= 12)中膜联蛋白V的水平,以评估第14天的细胞毒性和凋亡。第14天对另外3对角膜进行组织学评价。另外收集3对角膜,评估内皮细胞死亡标志物(casp3和BID, N=3),并在第7天使用RT-qPCR检测内皮细胞功能(ATP1A1、AQP1和SLC4A4, N=3, SLC4A4)。初步结果显示,与DCV相比,SCV储存的角膜钮扣在所有时间点的角膜中央厚度均无显著差异(p=0.648, p=0.295, p=0.180)。各时间点各组间EC密度差异无统计学意义(p=0.451, p=0.573, p=0.666)。在DCV和SCV中保存14天后,光镜下组织病理学切片显示基质肿胀或内皮细胞丢失无差异。内皮细胞死亡和功能的标志物没有发现差异。在为期两周的组织病理学检查中,DCV在角膜中央厚度、内皮细胞损失或间质肿胀方面没有表现出差异,因此DCV是一种安全可行的角膜纽扣储存方法。DCV为移植的人类角膜储存提供了另一种平台,并允许在每个隔室中使用定制的介质。DCV可以作为未来离体研究的平台,包括探索和开发定制保存解决方案,如选择性使用抗真菌添加剂和其他靶向干预措施。
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
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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