人工泪液和角膜上皮干燥保护

J. Ubels, Mark D. Aupperlee, D. Meadows
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引用次数: 2

摘要

干燥环境下眼表的干燥是干眼症患者不适的因素之一。采用体内干燥模型,考察人工泪液产品对长时间干燥暴露时眼表损伤的预防效果。将一滴人工泪液或晶状体再润湿液滴在麻醉兔的眼睛上,用窥镜保持眼睛睁开2小时。干燥的眼睛睁开2小时,不使用泪液。BSS用1%亚甲基蓝染色眼睛。Naïve对照眼在没有事先干燥的情况下用亚甲基蓝染色。对角膜染色面积的百分率进行评分,用丙酮:饱和硫酸钠(7:3)提取角膜中央一块8mm的钮扣。在660 nm处测定提取物的吸光度。提取物分析表明,五种泪液产品中有四种提供了完全保护(与naïve对照组没有区别),而一种低渗溶液提供了部分保护(摄取不同于干燥和naïve角膜)。含有EDTA的晶状体再润湿液不能保护角膜免受干燥。该体内模型可用于评估人工泪液在长时间干燥暴露期间保护角膜上皮免受损伤的能力。该方法可用于测试泪液成分的毒性,用于新的泪液配方的临床前评估,并可用于预测产品在临床使用中的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ARTIFICIAL TEAR SOLUTIONS AND PROTECTION OF THE CORNEAL EPITHELIUM FROM DESICCATION
Desiccation of the ocular surface in dry environments is one of the factors contributing to discomfort in dry eye patients. An in vivo desiccation model was used to test efficacy of artificial tear products for prevention of ocular surface damage during extended desiccating exposure. One drop of an artificial tear or a lens rewetting solution was placed on the eye of an anesthetized rabbit and the eye was held open with a speculum for 2 hr. Desiccated eyes were held open for 2 hr without application of a tear solution. Eyes were stained with 1% methylene blue in BSS. Naïve control eyes were stained with methylene blue without prior desiccation. The percentage of corneal area stained was scored and a 8-mm button of central cornea was extracted in acetone:saturated sodium sulfate (7:3). Absorbance of extracts was measured at 660 nm. Extract analysis showed that four of the five tear products tested offered complete protection from desiccation (not different from naïve control), while one solution, which was hypotonic, offered partial protection (uptake different from desiccated and naïve corneas). The lens rewetting solution, which contains EDTA, did not protect the cornea from desiccation. This in vivo model is useful in evaluating artificial tear solutions for their ability to protect the corneal epithelium from damage during prolonged desiccating exposure. This method can be used to test toxicity of tear solution components, for preclinical evaluation of new tear formulas and may be useful for prediction of product efficacy in clinical use.
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