TY - JOUR
T1 - Liposome Encapsulation Enhances Ripasudil Therapeutic Efficacy Against Proliferative Vitreoretinal Diseases
T2 - Implications in Advanced Ocular Treatment
AU - Ji, Rui
AU - Ishikawa, Keijiro
AU - Tan, Wei
AU - Mori, Kenichiro
AU - Tsukamoto, Ryotaro
AU - Matsunaga, Naoya
AU - Kiyohara, Kohei
AU - Fukuda, Yosuke
AU - Wada, Iori
AU - Isobe, Tomoyuki
AU - Tanihara, Tomohito
AU - Yoshida, Yuya
AU - Mayanagi, Kouta
AU - Oyama, Kosuke
AU - Terada, Yuma
AU - Otsuki, Kaita
AU - Hamamura, Kengo
AU - Kikuchi, Hiroshi
AU - Nakao, Shintaro
AU - Yoshida, Shigeo
AU - Kannan, Ram
AU - Ohdo, Shigehiro
AU - Sonoda, Koh Hei
N1 - Publisher Copyright:
Copyright 2025 The Authors.
PY - 2025/6
Y1 - 2025/6
N2 - 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.
AB - 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.
KW - age-related macular degeneration (AMD)
KW - fibrosis
KW - proliferative vitreoretinopathy (PVR)
UR - https://www.scopus.com/pages/publications/105008668068
UR - https://www.scopus.com/pages/publications/105008668068#tab=citedBy
U2 - 10.1167/iovs.66.6.56
DO - 10.1167/iovs.66.6.56
M3 - Article
C2 - 40525920
AN - SCOPUS:105008668068
SN - 0146-0404
VL - 66
JO - Investigative Ophthalmology and Visual Science
JF - Investigative Ophthalmology and Visual Science
IS - 6
M1 - 56
ER -