Institute of Cardiovascular Diseases, Xiamen Cardiovascular Hospital of Xiamen University, School of Medicine, Xiamen University, 2999 Jinshan Road, Huli District, Xiamen, China 361006.
ACS Nano. 2022 Feb 22;16(2):2330-2344. doi: 10.1021/acsnano.1c08538. Epub 2022 Feb 9.
Utilizing neutrophils (NEs) to target and deliver nanodrugs to inflammation sites has received considerable attention. NEs are involved in the formation and development of thrombosis by transforming into neutrophil extracellular traps (NETs); this indicates that NEs may be a natural thrombolytic drug delivery carrier. However, NEs lack an effective power system to overcome blood flow resistance and enhance targeting efficiency. Herein, we report the application of a urease catalysis micromotor powered NEs nanodrug delivery system to promote thrombolysis and suppress rethrombosis. The urease micromotor powered Janus NEs (UM-NEs) were prepared by immobilizing the enzyme asymmetrically onto the surface of natural NEs and then loading urokinase (UK) coupled silver (Ag) nanoparticles (Ag-UK) to obtain the UM-NEs (Ag-UK) system. Urease catalytic endogenous urea is used to generate thrust by producing ammonia and carbon dioxide, which propels NEs actively targeting the thrombus. The UM-NEs (Ag-UK) can be activated by enriched inflammatory cytokines to release NETs at the thrombosis site, resulting in a concomitant release of Ag-UK. Ag-UK induces thrombolysis to restore vascular recanalization. This urease micromotor-driven NEs drug delivery system can significantly reduce the hemorrhagic side effects, promote thrombolysis, and inhibit rethrombosis with high bioavailability and biosafety, which can be used for the treatment of thrombotic diseases.
利用嗜中性粒细胞 (NEs) 靶向并将纳米药物递送至炎症部位已受到广泛关注。NEs 通过转化为中性粒细胞胞外陷阱 (NETs) 参与血栓的形成和发展;这表明 NEs 可能是一种天然的溶栓药物递送载体。然而,NEs 缺乏有效的动力系统来克服血流阻力并提高靶向效率。在此,我们报告了一种脲酶催化微马达驱动的 NEs 纳米药物递送系统在促进溶栓和抑制再血栓形成方面的应用。通过将酶不对称地固定在天然 NEs 的表面,然后负载尿激酶 (UK) 偶联的银 (Ag) 纳米颗粒 (Ag-UK),制备了脲酶微马达驱动的 Janus NEs (UM-NEs),得到了 UM-NEs (Ag-UK) 系统。脲酶催化内源性尿素通过产生氨和二氧化碳产生推力,从而主动推动靶向血栓的 NEs。UM-NEs (Ag-UK) 可被富含炎症细胞因子激活,在血栓部位释放 NETs,同时释放 Ag-UK。Ag-UK 诱导溶栓以恢复血管再通。这种脲酶微马达驱动的 NEs 药物递送系统具有较高的生物利用度和生物安全性,可显著减少出血副作用,促进溶栓,并抑制再血栓形成,可用于治疗血栓性疾病。