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非诺贝特纳米乳滴眼液对视网膜血管渗漏和新生血管形成的治疗作用

Therapeutic Effects of Fenofibrate Nano-Emulsion Eye Drops on Retinal Vascular Leakage and Neovascularization.

作者信息

Huang Li, Liang Wentao, Zhou Kelu, Wassel Ronald A, Ridge Zachary D, Ma Jian-Xing, Wang Bing

机构信息

Department of Ophthalmology, Fujian Medical University Union Hospital, 29 Xinquan Road, Gulou District, Fuzhou 350001, China.

Department of Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.

出版信息

Biology (Basel). 2021 Dec 15;10(12):1328. doi: 10.3390/biology10121328.

Abstract

Macular edema caused by retinal vascular leakage and ocular neovascularization are the leading causes of severe vision loss in diabetic retinopathy (DR) and age-related macular degeneration (AMD) patients. Oral administration of fenofibrate, a PPARα agonist, has shown therapeutic effects on macular edema and retinal neovascularization in diabetic patients. To improve the drug delivery to the retina and its efficacy, we have developed a nano-emulsion-based fenofibrate eye drop formulation that delivered significantly higher amounts of the drug to the retina compared to the systemic administration, as measured by liquid chromatography-mass spectrometer (LC-MS). The fenofibrate eye drop decreased leukocytes adherent to retinal vasculature and attenuated overexpression of multiple inflammatory factors in the retina of very low-density lipoprotein receptor knockout () mice, a model manifesting AMD phenotypes, and streptozotocin-induced diabetic rats. The fenofibrate eye drop also reduced retinal vascular leakage in these models. The laser-induced choroidal neovascularization was also alleviated by the fenofibrate eye drop. There were no detectable ocular toxicities associated with the fenofibrate eye drop treatment. These findings suggest that fenofibrate can be delivered efficiently to the retina through topical administration of the nano-emulsion eye drop, which has therapeutic potential for macular edema and neovascularization.

摘要

视网膜血管渗漏和眼部新生血管形成所引起的黄斑水肿是糖尿病性视网膜病变(DR)和年龄相关性黄斑变性(AMD)患者严重视力丧失的主要原因。口服非诺贝特(一种PPARα激动剂)已显示出对糖尿病患者黄斑水肿和视网膜新生血管形成具有治疗作用。为了提高药物向视网膜的递送及其疗效,我们开发了一种基于纳米乳液的非诺贝特滴眼液制剂,通过液相色谱 - 质谱仪(LC - MS)测量,与全身给药相比,该制剂向视网膜递送的药物量显著更高。非诺贝特滴眼液减少了黏附于视网膜血管系统的白细胞,并减弱了极低密度脂蛋白受体敲除()小鼠(一种表现出AMD表型的模型)和链脲佐菌素诱导的糖尿病大鼠视网膜中多种炎症因子的过表达。非诺贝特滴眼液还减少了这些模型中的视网膜血管渗漏。非诺贝特滴眼液也减轻了激光诱导的脉络膜新生血管形成。非诺贝特滴眼液治疗未发现可检测到的眼部毒性。这些发现表明,通过纳米乳液滴眼液局部给药可将非诺贝特有效地递送至视网膜,其对黄斑水肿和新生血管形成具有治疗潜力。

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