Department of Ophthalmology, Paulista School of Medicine, Federal University of Sao Paulo - UNIFESP, Sao Paulo, SP, Brazil.
PLoS One. 2013 Jun 13;8(6):e66408. doi: 10.1371/journal.pone.0066408. Print 2013.
Corneal collagen cross-linking (CXL) has been described as a promising therapy for keratoconus. According to standard CXL protocol, epithelium should be debrided before treatment to allow penetration of riboflavin into the corneal stroma. However, removal of the epithelium can increase procedure risks. In this study we aim to evaluate stromal penetration of a biocompatible riboflavin-based nanoemulsion system (riboflavin-5-phosphate and riboflavin-base) in rabbit corneas with intact epithelium. Two riboflavin nanoemulsions were developed. Transmittance and absorption coefficient were measured on corneas with intact epithelia after 30, 60, 120, 180, and 240 minutes following exposure to either the nanoemulsions or standard 0.1% or 1% riboflavin-dextran solutions. For the nanoemulsions, the epithelium was removed after measurements to assure that the riboflavin had passed through the hydrophobic epithelium and retained within the stroma. Results were compared to de-epithelialized corneas exposed to 0.1% riboflavin solution and to the same riboflavin nanoemulsions for 30 minutes (standard protocol). Mean transmittance and absorption measured in epithelialized corneas receiving the standard 0.1% riboflavin solution did not reach the levels found on the debrided corneas using the standard technique. Neither increasing the time of exposure nor the concentration of the riboflavin solution from 0.1% to 1% improved riboflavin penetration through the epithelium. When using riboflavin-5-phosphate nanoemulsion for 240 minutes, we found no difference between the mean absorption coefficients to the standard cross-linking protocol (p = 0.54). Riboflavin nanoemulsion was able to penetrate the corneal epithelium, achieving, after 240 minutes, greater stromal concentration when compared to debrided corneas with the standard protocol (p = 0.002). The riboflavin-5-phosphate nanoemulsion diffused better into the stroma than the riboflavin-base nanoemulsion.
角膜胶原交联 (CXL) 已被描述为治疗圆锥角膜的一种有前途的疗法。根据标准 CXL 方案,在治疗前应去除上皮以允许核黄素进入角膜基质。然而,去除上皮会增加手术风险。在这项研究中,我们旨在评估具有完整上皮的兔角膜中生物相容的核黄素基纳米乳液系统(核黄素-5-磷酸和核黄素基)的基质穿透性。开发了两种核黄素纳米乳液。在用纳米乳液或标准 0.1%或 1%核黄素-葡聚糖溶液暴露 30、60、120、180 和 240 分钟后,测量具有完整上皮的角膜的透光率和吸收系数。对于纳米乳液,在测量后去除上皮,以确保核黄素已通过疏水性上皮并保留在基质中。将结果与暴露于 0.1%核黄素溶液的去上皮化角膜进行比较,并与相同的核黄素纳米乳液进行 30 分钟(标准方案)比较。在用标准 0.1%核黄素溶液处理的上皮化角膜中测量的平均透光率和吸收率均未达到使用标准技术对去上皮化角膜的测量值。增加暴露时间或将核黄素溶液的浓度从 0.1%增加到 1%都不能提高核黄素通过上皮的穿透率。当使用核黄素-5-磷酸纳米乳液 240 分钟时,我们发现与标准交联方案的平均吸收系数没有差异(p=0.54)。核黄素纳米乳液能够穿透角膜上皮,在 240 分钟后与标准方案的去上皮化角膜相比,达到更大的基质浓度(p=0.002)。核黄素-5-磷酸纳米乳液比核黄素基纳米乳液更能扩散到基质中。