From Consiglio Nazionale delle Ricerche, Istituto per i Processi Chimico-Fisici (G. Lombardo, Micali, Villari, Leone), Messina, Vision Engineering Italy srl (G. Lombardo), and Fondazione G.B. Bietti IRCCS (Serrao, M. Lombardo), Rome, and Sooft Italia Spa (Rusciano), Montegiorgio, Italy.
From Consiglio Nazionale delle Ricerche, Istituto per i Processi Chimico-Fisici (G. Lombardo, Micali, Villari, Leone), Messina, Vision Engineering Italy srl (G. Lombardo), and Fondazione G.B. Bietti IRCCS (Serrao, M. Lombardo), Rome, and Sooft Italia Spa (Rusciano), Montegiorgio, Italy.
J Cataract Refract Surg. 2017 May;43(5):680-686. doi: 10.1016/j.jcrs.2017.03.026.
To determine the intrastromal concentration of riboflavin in nanotechnology-based transepithelial corneal crosslinking.
Consiglio Nazionale delle Ricerche, Messina, Italy.
Experimental study.
Six human donor sclerocorneal tissues were used to evaluate penetration of nanotechnology-based riboflavin 0.1% solution in the stroma through the intact epithelium. Three additional tissues were deepithelialized and soaked with dextran 20.0%-enriched riboflavin 0.1% solution for 30 minutes. After corneal soaking with riboflavin, all tissues were irradiated using a 10 mW/cm device for 9 minutes. Two-photon emission fluorescence (TPEF) axial scanning measurements were collected in all specimens before treatment and immediately after corneal soaking with riboflavin and ultraviolet-A (UVA) irradiation of the cornea. The absorbance spectra of each tissue were collected at the same time intervals. The TPEF signals and absorbance spectra were used to calculate the concentration-depth profile of riboflavin in the corneal stroma during treatments.
The mean stromal riboflavin concentration was 0.008% ± 0.003% (SD) and 0.017% ± 0.001% after transepithelial soaking with the nanotechnology-based solution and standard soaking, respectively (P = .001). After UVA irradiation of the cornea, the mean consumption of riboflavin was 52% ± 13% and 67% ± 2% in the study group and control group, respectively (P < .01).
The nanotechnology-based platform was effective in enriching the anterior stroma with riboflavin through the intact epithelium, although the riboflavin concentration-depth profile rapidly decreased across the mid and posterior stroma. The treatment-induced stiffening effect on the corneal stroma was not assessed in this study.
确定基于纳米技术的经上皮角膜交联术的基质内核黄素浓度。
意大利墨西拿的意大利国家研究委员会。
实验研究。
使用 6 个人供体硬角膜组织评估纳米技术 0.1%核黄素溶液通过完整上皮穿透基质的情况。另外 3 个组织去上皮化并浸泡在富含葡聚糖 20.0%-的 0.1%核黄素溶液中 30 分钟。角膜浸泡核黄素后,所有组织均使用 10 mW/cm 的设备照射 9 分钟。所有标本在治疗前和角膜浸泡核黄素及角膜紫外线-A(UVA)照射后立即进行双光子发射荧光(TPEF)轴向扫描测量。同时收集各组织的吸收光谱。TPEF 信号和吸收光谱用于计算治疗过程中角膜基质中核黄素的浓度-深度分布。
经上皮浸泡纳米技术溶液和标准浸泡后,基质核黄素的平均浓度分别为 0.008%±0.003%(SD)和 0.017%±0.001%(P=0.001)。角膜 UVA 照射后,实验组和对照组核黄素的平均消耗分别为 52%±13%和 67%±2%(P<0.01)。
尽管核黄素浓度-深度分布在中后部基质中迅速下降,但基于纳米技术的平台通过完整的上皮有效地使前基质富含核黄素。本研究未评估治疗对角膜基质的僵硬效应。