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脂质体包封增强了ripasudil对增殖性玻璃体视网膜疾病的治疗效果:对晚期眼部治疗的启示。

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

作者信息

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

机构信息

Department of Ophthalmology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Department of Clinical Pharmacokinetics, Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Invest Ophthalmol Vis Sci. 2025 Jun 2;66(6):56. doi: 10.1167/iovs.66.6.56.

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.

摘要

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),在疾病晚期会因视网膜纤维膜的形成而带来巨大挑战。目前的治疗方式,包括针对PVR的手术干预和针对nAMD的抗血管内皮生长因子治疗,无法有效控制与视网膜色素上皮(RPE)细胞上皮-间充质转化(EMT)相关的眼内纤维化。通过药物筛选,我们确定Rho激酶抑制剂法舒地尔是RPE-EMT的显著抑制剂。然而,小分子药物在玻璃体内的半衰期较短,再加上法舒地尔在眼内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。考虑到纳米技术在提高药物稳定性、细胞摄取以及控释方面的进展,我们旨在通过脂质体包封来提高法舒地尔的疗效。

方法

对法舒地尔进行脂质体包封后,我们进行了全面的体内和体外分析以及药代动力学研究。

结果

脂质体包封的法舒地尔(Lipo-Ripa)在晚期AMD模型中显示视网膜下纤维化显著减少,并且在兔体内对PVR进展的抑制作用比单独使用法舒地尔更有效。药代动力学研究表明,Lipo-Ripa在玻璃体和视网膜中的保留能力有所提高,同时通过RPE屏障的通透性降低,细胞摄取增加。这些特性导致眼内组织中的药物浓度随时间持续升高。

结论

我们的研究结果表明,法舒地尔的脂质体包封可提高药物的生物利用度和有效性,为增殖性玻璃体视网膜病变的治疗提供了一种有前景的创新治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f28/12178431/e0a5298fc778/iovs-66-6-56-f001.jpg

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