Ophthalmic Drops with Nanoparticles Derived from a Natural Product for Treating Age-Related Macular Degeneration

眼药水 下降(电信) 黄斑变性 材料科学 生物物理学 眼科 药理学 医学 生物 电信 计算机科学
作者
Guang Xin,Ming Zhang,Zhihui Zhong,Li Tang,Yuliang Feng,Zeliang Wei,Shiyi Li,Youping Li,Junhua Zhang,Boli Zhang,Meng Zhang,Nelson L. Rowell,Zhen Chen,Hai Niu,Kui Yu,Wen Qing Huang
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:12 (52): 57710-57720 被引量:29
标识
DOI:10.1021/acsami.0c17296
摘要

There is a continuing, urgent need for an ophthalmic (eye) drop for the clinical therapy of age-related macular degeneration (AMD), a leading cause of blindness. Here, we report the first formulation of an eye drop that is effective via autophagy for AMD treatment. This eye drop is based on a single natural product derivative (ACD), which is an amphiphilic molecule containing a 6-aminohexanoate group (H 2 N(CH 2 ) 5 COO−). We demonstrate that this eye drop reverses the abnormal angiogenesis induced in a primate model of AMD that has the pathological characteristics close to that of human AMD. The ACD molecule was self-assembled in an aqueous environment leading to nanoparticles (NPs) about 9.0 nm in diameter. These NPs were encapsulated in calcium alginate hydrogel. The resulting eye drop effectively slowed the release of ACD and displayed extended release periods in both simulated blood (pH 7.4) and inflammatory (pH 5.2) environments. We show that the eye drop penetrated both the corneal and blood–eye barriers and reached the fundus. With low cellular toxicity, the drop targeted S1,25D 3 -membrane-associated rapid response steroid-binding protein (1,25D 3 -MARRS) promoting autophagy in a dose-dependent manner. In addition, the drop inhibited cell migration and tubular formation. On the other hand, when protein 1,25D 3 -MARRS was knocked down, the eye drop did not exhibit such inhibition functionalities. Our study indicates that the 6-aminohexanoate group on self-assembled NPs encapsulated in hydrogel leads to the positive in vivo outcomes. The present formulation offers a promising approach for clinical treatment of human AMD.
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