使用不同的临床眼科制剂实时监测核黄素浓度,用于外显子脱落角膜交联和外显子接合角膜交联

Marco Lombardo, Sebastiano Serrao, Giuseppe Massimo Bernava, Rita Mencucci, Mario Fruschelli, Giuseppe Lombardo
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摘要

方法将 32 例眼库人类供体角膜平均随机分为 8 组,第 1 至 3 组和第 4 至 8 组分别进行核黄素外显子注射和外显子注射。按照生产商的说明将核黄素眼药水涂抹在角膜上。在浸泡期间的预设时间间隔内,使用治疗仪 UV-A 装置(C4V CHROMO4VIS,Regensight srl,意大利)估算进入角膜的核黄素量,并以核黄素分数(d.u.)表示。此外,还通过光谱吸光技术(AvaLight-DH-S-BAL,Avantes)测量了角膜核黄素浓度(以 µg/cm3 表示),对治疗仪的测量结果进行了外部验证。结果 在外显给药方案的浸泡时间结束时,核黄素平均得分从 0.77 ± 0.38(角膜核黄素平均浓度为 213 ± 190 µg/cm3)到 1.79 ± 0.07(554 ± 103 µg/cm3)不等。在外延给药方案中,浸泡时间结束时核黄素的平均得分从 0.17 ± 0.01 到 0.67 ± 0.19(角膜核黄素浓度从 6 ± 5 µg/cm3 到 122 ± 39 µg/cm3)不等。结论实时治疗仪成像为评估角膜交联浸润期核黄素在人角膜中的渗透情况提供了一种准确的方法,而无需考虑给药方案。在外延-关闭和外延-开启给药方案中,临床可用的眼科制剂在角膜核黄素浓度方面存在很大差异。
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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Real-time monitoring of riboflavin concentration using different clinically available ophthalmic formulations for epi-off and epi-on corneal cross-linking

Purpose

To assess the feasibility of theranostics to determine the riboflavin concentration in the cornea using clinically available ophthalmic formulations during epithelium-off (epi-off) and transepithelial (epi-on) corneal cross-linking procedures.

Methods

Thirty-two eye bank human donor corneas were equally randomized in eight groups; groups 1 to 3 and groups 4 to 8 underwent epi-off and epi-on delivery of riboflavin respectively. Riboflavin ophthalmic solutions were applied onto the cornea according to the manufacturers’ instructions. The amount of riboflavin into the cornea was estimated, at preset time intervals during imbibition time, using theranostic UV-A device (C4V CHROMO4VIS, Regensight srl, Italy) and expressed as riboflavin score (d.u.). Measurements of corneal riboflavin concentration (expressed as µg/cm3) were also performed by spectroscopy absorbance technique (AvaLight-DH-S-BAL, Avantes) for external validation of theranostic measurements.

Results

At the end of imbibition time in epi-off delivery protocols, the average riboflavin score ranged from 0.77 ± 0.38 (the average corneal riboflavin concentration was 213 ± 190 µg/cm3) to 1.79 ± 0.07 (554 ± 103 µg/cm3). In epi-on delivery protocols, the average riboflavin score ranged from 0.17 ± 0.01 to 0.67 ± 0.19 (corneal riboflavin concentration ranged from 6 ± 5 µg/cm3 to 122 ± 39 µg/cm3) at the end of imbibition time. A statistically significant linear correlation (P ≤ 0.05) was found between the theranostic and spectrophotometry measurements in all groups.

Conclusions

Real-time theranostic imaging provided an accurate strategy for assessing permeation of riboflavin into the human cornea during the imbibition phase of corneal cross-linking, regardless of delivery protocol. A large variability in corneal riboflavin concentration exists between clinically available ophthalmic formulations both in epi-off and epi-on delivery protocols.

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