Liposome Encapsulation Enhances Ripasudil Therapeutic Efficacy Against Proliferative Vitreoretinal Diseases: Implications in Advanced Ocular Treatment.

IF 4.7 2区 医学 Q1 OPHTHALMOLOGY
Rui Ji, Keijiro Ishikawa, Wei Tan, Kenichiro Mori, Ryotaro Tsukamoto, Naoya Matsunaga, Kohei Kiyohara, Yosuke Fukuda, Iori Wada, Tomoyuki Isobe, Tomohito Tanihara, Yuya Yoshida, Kouta Mayanagi, Kosuke Oyama, Yuma Terada, Kaita Otsuki, Kengo Hamamura, Hiroshi Kikuchi, Shintaro Nakao, Shigeo Yoshida, Ram Kannan, Shigehiro Ohdo, Koh-Hei Sonoda
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Abstract

Purpose: Proliferative vitreoretinal diseases, such as proliferative vitreoretinopathy (PVR) and neovascular age-related macular degeneration (nAMD), pose substantial challenges in their advanced stages owing to the development of retinal fibrous membranes. Current therapeutic modalities, including surgical interventions for PVR and antivascular endothelial growth factor therapy for nAMD, cannot effectively manage intraocular fibrosis associated with epithelial-to-mesenchymal transition (EMT) in retinal pigment epithelium (RPE) cells. Through drug screening, we identified ripasudil, a Rho-kinase inhibitor, as a remarkable suppressor of RPE-EMT. However, the short vitreal half-lives of small-molecule drugs, coupled with the limited stability of ripasudil in the ocular environment, impede its application in vitreoretinal diseases. Considering the advances in nanotechnology-assisted improvement in drug stability and cellular uptake as well as controlled release, we aimed to enhance the efficacy of ripasudil through liposome encapsulation.

Methods: After ripasudil encapsulation, we performed comprehensive in vivo and in vitro analyses and pharmacokinetic studies.

Results: Liposome-encapsulated ripasudil (Lipo-Ripa) demonstrated a substantial reduction in subretinal fibrosis in an advanced AMD model and more effective inhibition of PVR progression in rabbits than that induced by ripasudil alone. Pharmacokinetic studies revealed that Lipo-Ripa exhibited improved retention capacity in the vitreous and retina, alongside reduced permeability through the RPE barrier and increased cellular uptake. These characteristics resulted in a sustained elevation of drug concentration within the ocular tissues over time.

Conclusions: Our findings suggest that liposomal encapsulation of ripasudil supports enhanced bioavailability and effectiveness of the drug, presenting a promising innovative therapeutic approach for the treatment of proliferative vitreoretinopathy.

脂质体包封增强利帕舒地尔治疗增殖性玻璃体视网膜疾病的疗效:在眼部高级治疗中的意义。
目的:增殖性玻璃体视网膜疾病,如增殖性玻璃体视网膜病变(PVR)和新生血管性年龄相关性黄斑变性(nAMD),由于视网膜纤维膜的发育,在其晚期提出了实质性的挑战。目前的治疗方式,包括手术治疗PVR和抗血管内皮生长因子治疗nAMD,不能有效地控制视网膜色素上皮(RPE)细胞上皮-间质转化(EMT)相关的眼内纤维化。通过药物筛选,我们发现rho激酶抑制剂利帕舒地尔是一种显著的RPE-EMT抑制剂。然而,小分子药物的玻璃体半衰期短,加上利帕舒地尔在眼环境中的稳定性有限,阻碍了其在玻璃体视网膜疾病中的应用。考虑到纳米技术在药物稳定性、细胞摄取和控释方面的进步,我们旨在通过脂质体包封来提高利帕舒地尔的疗效。方法:利帕舒地尔胶囊化后,进行全面的体内外分析和药代动力学研究。结果:脂质体包膜利帕舒地尔(lipo质体- ripa)在晚期AMD模型中可显著减少视网膜下纤维化,并且比单独使用利帕舒地尔更有效地抑制兔PVR的进展。药代动力学研究表明,Lipo-Ripa在玻璃体和视网膜中表现出更好的保留能力,同时降低了通过RPE屏障的渗透性,增加了细胞摄取。随着时间的推移,这些特征导致眼部组织内药物浓度持续升高。结论:我们的研究结果表明,脂质体包封利帕舒地尔支持提高药物的生物利用度和有效性,为治疗增殖性玻璃体视网膜病变提供了一种有希望的创新治疗方法。
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来源期刊
CiteScore
6.90
自引率
4.50%
发文量
339
审稿时长
1 months
期刊介绍: Investigative Ophthalmology & Visual Science (IOVS), published as ready online, is a peer-reviewed academic journal of the Association for Research in Vision and Ophthalmology (ARVO). IOVS features original research, mostly pertaining to clinical and laboratory ophthalmology and vision research in general.
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