视网膜
视网膜
纳米医学
体内
黄斑变性
视网膜变性
生物相容性
玻璃体内给药
化学
药理学
白藜芦醇
纳米技术
医学
眼科
材料科学
纳米颗粒
生物
生物化学
神经科学
有机化学
生物技术
作者
Nguyen Duc Dung,Li‐Jyuan Luo,Chia-Jung Yang,Jui‐Yang Lai
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-12-16
卷期号:17 (1): 168-183
被引量:89
标识
DOI:10.1021/acsnano.2c05824
摘要
The development of therapeutics for effective treatments of retinal diseases is significantly constrained by various biological barriers. We herein report a nanomedicine strategy to develop nanotherapeutics featured with not only high retinal permeability but also sustained bioactive delivery. Specifically, the nanotherapeutics are rationally designed via aminolysis of resveratrol-encapsulated polycaprolactone nanoparticles (R@PCL NPs), followed by the formation of amide linkages with carboxyl-terminated transacting activator of transcription cell penetrating peptide (T) and metformin (M). The R@PCL-T/M NP nanotherapeutics are demonstrated in vitro to possess persistent drug release profiles, good ocular biocompatibility, and potent bioactive activities for targeting prevailing risk factors associated with retinal diseases. In vivo studies indicate that single-dose intravitreal administration of the R@PCL-T/M NPs can effectively improve retinal permeability (∼15-fold increase), prevent loss of endogenous antioxidants, and suppress the growth of abnormal vessels in the retina with macular degeneration for 56 days. This high treatment efficacy can be ascribed to the enhanced retinal permeability of the nanotherapeutics in conjunction with the sustained pharmacological activity of the dual drugs (R and M) in the retinal pigment epithelial region. These findings show a great promise for the development of pharmacological nanoformulations capable of targeting the retina and thereby treating complex posterior segment diseases with improved efficacies.
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