A novel, liposome-loaded, injectable hydrogel for enhanced treatment of choroidal neovascularization by sub-tenon's injection

脉络膜新生血管 脂质体 医学 药理学 舒尼替尼 光动力疗法 新生血管 药物输送 血管生成 癌症研究 眼科 视网膜 化学 癌症 内科学 有机化学 生物化学
作者
Jingkun Li,Qiang Tian,Huimin Sun,Ying Zhang,Xiaoyan Yang,Prabhleen Kaur,Rong Yuan,Yanan Fang,Hongmei Yan,Xiyou Du,Lin Ye,Guangxi Zhai
出处
期刊:Materials Today Nano [Elsevier]
卷期号:20: 100264-100264 被引量:7
标识
DOI:10.1016/j.mtnano.2022.100264
摘要

As a common multifactor fundus lesion, choroidal neovascularization (CNV) has become the leading cause of severe vision loss in the elderly. The mainstay treatment is an invasive intravitreal injection of anti-VEGF drug, which leads to a short half-life, incomplete response, and severe ocular complications. In this work, we have developed a novel, liposome-loaded, injectable hydrogel ([email protected]) by a minimally invasive sub-tenon's injection for CNV treatment. First, the multitarget angiogenic inhibitor (sunitinib) and hypoxia-inducible factor inhibitor (acriflavine) were co-loaded in the liposome, which was then loaded in the injectable hydrogel. The in vitro results showed that the [email protected] group had a strong anti-angiogenesis effect. After sub-tenon's injection, the hydrogel endowed the drug-loaded liposome with a longer retention time in the target area. In the CNV model, [email protected] showed a significant anti-CNV effect, which was superior to that of intravitreal injection of a commercial product (Conbercept). Exploration of the molecular mechanism revealed that [email protected] did not only inhibit CNV through the AKT/mTOR/HIF-1α/VEGF signal pathways but also inhibit VEGF R1 and VEGF R2. In conclusion, this novel drug delivery system, combining the merits of the liposome and hydrogel, showed an enhanced anti-CNV effect, thus providing a new and minimally invasive alternative for the treatment of neovascular ocular diseases.
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