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脂质纳米粒(LNPs)共递送 microRNA-150 和槲皮素用于年龄相关性黄斑变性(AMD)的靶向治疗。

Co-delivery of microRNA-150 and quercetin by lipid nanoparticles (LNPs) for the targeted treatment of age-related macular degeneration (AMD).

机构信息

School of Basic Medicine, Institute for Advanced Study, Chengdu University, Chengdu 610106, People's Republic of China.

School of Food and Biological Engineering, Chengdu University, Chengdu 610106, People's Republic of China; State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611130, People's Republic of China.

出版信息

J Control Release. 2023 Mar;355:358-370. doi: 10.1016/j.jconrel.2023.01.080. Epub 2023 Feb 9.

Abstract

Age-related macular degeneration (AMD) is characterized by choroidal neovascularization (CNV), which leads to severe vision loss in middle-aged and elderly patients. Current treatments for CNV show weak, transient efficacy, and they can cause several adverse effects. A potential new treatment is to use microRNA-150 (mR150), which regulates physiological and pathological angiogenesis by modulating the expression of CXCR4 at the post-transcriptional level. Here, we developed solid lipid nanoparticles that we modified with an Asp-Gly-Arg peptide to target endothelial cells during abnormal angiogenesis, then we co-loaded them with mR150 and the anti-angiogenic drug quercetin. The resulting nanoparticles had an average size around 200 nm and showed strong ability to target the fundus and inhibit CNV for up to two weeks in a mouse model without causing retinal toxicity. They significantly enhanced the uptake of mR150 in vitro compared to free mR150 or nanoparticles without peptide. Our study suggests that co-administration of mR150 and quercetin has potential for treating age-related macular degeneration and that nanoparticles modified with Asp-Gly-Arg peptide are an effective platform for the co-delivery of small-molecule and nucleic acid drugs via intravitreal injection.

摘要

年龄相关性黄斑变性(AMD)的特征是脉络膜新生血管(CNV),这会导致中年和老年患者严重的视力丧失。目前治疗 CNV 的方法效果较弱且短暂,并且可能会引起多种不良反应。一种潜在的新治疗方法是使用 microRNA-150(mR150),它通过调节 CXCR4 的转录后表达来调节生理和病理血管生成。在这里,我们开发了固体脂质纳米粒,并用天冬氨酸-甘氨酸-精氨酸(Asp-Gly-Arg)肽对其进行修饰,以在异常血管生成期间靶向内皮细胞,然后将其与 mR150 和抗血管生成药物槲皮素共同负载。所得纳米粒的平均粒径约为 200nm,在不引起视网膜毒性的情况下,在小鼠模型中显示出强烈的靶向眼底和抑制 CNV 的能力,最长可达两周。与游离 mR150 或没有肽的纳米粒相比,它们显著增强了体外对 mR150 的摄取。我们的研究表明,mR150 和槲皮素的联合给药具有治疗年龄相关性黄斑变性的潜力,并且用 Asp-Gly-Arg 肽修饰的纳米粒是通过玻璃体内注射共递小分子和核酸药物的有效平台。

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