School of Medicine, Xiamen University Affiliated Xiamen Eye Center, Eye Institute of Xiamen University, Xiamen University, Xiamen, 361102, China.
Fujian Provincial Key Laboratory of Ophthalmology and Visual Science, Fujian Engineering and Research Center of Eye Regenerative Medicine, Xiamen, 361102, China.
J Nanobiotechnology. 2024 May 27;22(1):290. doi: 10.1186/s12951-024-02510-8.
Corneal neovascularization (CNV) is one of the common blinding factors worldwide, leading to reduced vision or even blindness. However, current treatments such as surgical intervention and anti-VEGF agent therapy still have some shortcomings or evoke some adverse effects. Recently, SU6668, an inhibitor targeting angiogenic tyrosine kinases, has demonstrated growth inhibition of neovascularization. But the hydrophobicity and low ocular bioavailability limit its application in cornea. Hereby, we proposed the preparation of SU6668 pure nanoparticles (NanoSU6668; size ~135 nm) using a super-stable pure-nanomedicine formulation technology (SPFT), which possessed uniform particle size and excellent aqueous dispersion at 1 mg/mL. Furthermore, mesenchymal stem cell membrane vesicle (MSCm) was coated on the surface of NanoSU6668, and then conjugated with TAT cell penetrating peptide, preparing multifunctional TAT-MSCm@NanoSU6668 (T-MNS). The T-MNS at a concentration of 200 µg/mL was treated for CNV via eye drops, and accumulated in blood vessels with a high targeting performance, resulting in elimination of blood vessels and recovery of cornea transparency after 4 days of treatment. Meanwhile, drug safety test confirmed that T-MNS did not cause any damage to cornea, retina and other eye tissues. In conclusion, the T-MNS eye drop had the potential to treat CNV effectively and safely in a low dosing frequency, which broke new ground for CNV theranostics.
角膜新生血管(CNV)是全球常见的致盲因素之一,可导致视力下降甚至失明。然而,目前的治疗方法,如手术干预和抗 VEGF 药物治疗,仍存在一些缺点或引发一些不良反应。最近,针对血管生成酪氨酸激酶的抑制剂 SU6668 已显示出对新生血管生长的抑制作用。但其疏水性和低眼部生物利用度限制了其在角膜中的应用。因此,我们提出使用超稳定纯纳米药物制剂技术(SPFT)制备 SU6668 纯纳米颗粒(NanoSU6668;大小约 135nm),该技术具有均匀的粒径和在 1mg/ml 时优异的水分散性。此外,间充质干细胞膜囊泡(MSCm)被包裹在 NanoSU6668 的表面,然后与 TAT 细胞穿透肽结合,制备多功能 TAT-MSCm@NanoSU6668(T-MNS)。浓度为 200μg/ml 的 T-MNS 通过滴眼剂治疗 CNV,并在血管中具有高靶向性能,导致血管消除,治疗 4 天后角膜透明度恢复。同时,药物安全性测试证实 T-MNS 不会对角膜、视网膜和其他眼部组织造成任何损伤。总之,T-MNS 滴眼剂具有以低剂量频率有效和安全治疗 CNV 的潜力,为 CNV 的治疗开辟了新途径。