Business Unit Pharma S.I.F.I. Spa Via E. Patti 36, Lavinaio, Aci S. Antonio, Catania, Italy.
Cornea. 2010 Jul;29(7):802-6. doi: 10.1097/ICO.0b013e3181ca327e.
The present investigation is aimed to evaluate the effect of a new lipid artificial tear on tear volume and ocular surface signs in a mouse model of dry eye and to test the hypothesis that the combined application with sodium hyaluronate can improve the performance of the treatments.
A new oil-in-water emulsion, a 0.2% sodium hyaluronate solution, or their combined administration were given to dry eye mice maintained in a controlled environment chamber and treated with scopolamine (0.75-mg transdermal patch). Mice were treated 4 times a day with (a) sodium hyaluronate, (b) emulsion, and (c) sodium hyaluronate followed by emulsion. A control group of mice exposed to controlled environment chamber remained untreated (CTRL+). Tear volume and corneal damage were assessed after 3 and 7 days of treatment by cotton thread test and fluorescein staining.
As regards tear volume, sodium hyaluronate did not show a statistically significant effect at either end point; the emulsion was effective after 7 days, whereas their combined administration counteracted the lacrimal decrease induced by the model both at 3 and 7 days. Corneal damage was reduced in all treated groups with respect to CTRL+. This effect was statistically significant after 3 days when the emulsion alone or in combination with sodium hyaluronate was used, while hyaluronate improved this clinical sign after 7 days.
Our data suggest that the new lipid tear substitute can be used to treat clinical signs of dry eye and that the combined administration with hyaluronate can decrease the lag time before the effect, when the evaporative and the aqueous-deficient components are present.
本研究旨在评估一种新型脂质人工泪液对干眼症小鼠泪液量和眼表体征的影响,并验证联合应用透明质酸钠可改善治疗效果的假设。
将一种新型水包油乳液、0.2%透明质酸钠溶液或两者联合应用于在环境受控室中维持的干眼症小鼠,并给予东莨菪碱(0.75mg 透皮贴剂)治疗。每天 4 次,用(a)透明质酸钠、(b)乳液和(c)透明质酸钠后用乳液对小鼠进行治疗。暴露于环境受控室但未经处理的一组小鼠作为对照组(CTRL+)。通过棉线试验和荧光素染色,在治疗 3 天和 7 天后评估泪液量和角膜损伤。
就泪液量而言,透明质酸钠在两个终点均未显示出统计学显著效果;乳液在第 7 天有效,而联合应用则在第 3 天和第 7 天均拮抗了模型引起的泪液减少。与 CTRL+相比,所有治疗组的角膜损伤均减少。当单独使用乳液或与透明质酸钠联合使用时,这种效果在第 3 天具有统计学意义,而在第 7 天,透明质酸钠可改善这一临床体征。
我们的数据表明,新型脂质人工泪替代物可用于治疗干眼症的临床体征,并且当存在蒸发和水缺乏成分时,联合应用透明质酸钠可以减少起效时间。