Ophthalmic Drops with Nanoparticles Derived from a Natural Product for Treating Age-Related Macular Degeneration.
Guang XinMing ZhangZhihui ZhongLi TangYuliang FengZeliang WeiShiyi LiYouping LiJunhua ZhangBoli ZhangMeng ZhangNelson RowellZhen ChenHai NiuKui YuWen HuangPublished in: ACS applied materials & interfaces (2020)
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 (H2N(CH2)5COO-). 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 S1,25D3-membrane-associated rapid response steroid-binding protein (1,25D3-MARRS) promoting autophagy in a dose-dependent manner. In addition, the drop inhibited cell migration and tubular formation. On the other hand, when protein 1,25D3-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.
Keyphrases
- cell migration
- age related macular degeneration
- endothelial cells
- drug delivery
- binding protein
- oxidative stress
- wound healing
- type diabetes
- ionic liquid
- mesenchymal stem cells
- metabolic syndrome
- stem cells
- vascular endothelial growth factor
- photodynamic therapy
- combination therapy
- optical coherence tomography
- induced pluripotent stem cells
- diabetic retinopathy
- cancer therapy
- sensitive detection
- insulin resistance
- room temperature
- hyaluronic acid
- cell therapy