Eyedrop-based macromolecular ophthalmic drug delivery for ocular fundus disease treatment

眼底(子宫) 眼球后段 医学 药物输送 眼科 糖尿病性视网膜病变 新生血管 视网膜 药品 脉络膜新生血管 药理学 视网膜 癌症研究 血管生成 材料科学 生物 纳米技术 内分泌学 糖尿病 神经科学
作者
Jingjing Shen,Huiqin Gao,Linfu Chen,Yutong Jiang,Shu Li,Yu Chao,Nanhui Liu,Yufei Wang,Ting Wei,Yan Liu,Jipeng Li,Muchao Chen,Jiafei Zhu,Juan Liang,Zhou Xiao-yu,Xiaofeng Zhang,Ping Gu,Qian Chen,Zhuang Liu
出处
期刊:Science Advances [American Association for the Advancement of Science]
卷期号:9 (4): eabq3104-eabq3104 被引量:67
标识
DOI:10.1126/sciadv.abq3104
摘要

Therapeutic antibodies are extensively used to treat fundus diseases by intravitreal injection, as eyedrop formulation has been rather challenging due to the presence of ocular barriers. Here, an innovative penetrating carrier was developed for antibody delivery in eyedrop formulations. We found that fluorocarbon-modified chitosan (FCS) would self-assemble with proteins to form nanocomplexes, which could effectively pass across the complicated ocular structure to reach the posterior eye segments in both mice and rabbits. In a choroidal melanoma–bearing mouse model, eyedrops containing FCS/anti-PDL1 could induce stronger antitumor immune responses than those triggered by intravenous injection of anti-PDL1. Moreover, in choroidal neovascularization–bearing mouse and rabbit models, FCS/anti-VEGFA eyedrops effectively inhibited vascular proliferation, achieving comparable therapeutic responses to those observed with intravitreal injection of anti-VEGFA. Our work presents an effective delivery carrier to treat fundus diseases using eyedrop of therapeutic proteins, which may enable at-home treatment of many eye diseases with great patient compliance.
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