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靶向纳米气泡的深穿透增强了溶栓能力的空化效应。

Deep Penetration of Targeted Nanobubbles Enhanced Cavitation Effect on Thrombolytic Capacity.

机构信息

Department of Ultrasound , Ningbo First Hospital , Ningbo 315010 , China.

Cixi Institute of Biomedical Engineering, CAS Key Laboratory of Magnetic Materials and Devices, Key Laboratory of Additive Manufacturing Materials of Zhejiang Province , Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences , Ningbo 315201 , China.

出版信息

Bioconjug Chem. 2020 Feb 19;31(2):369-374. doi: 10.1021/acs.bioconjchem.9b00653. Epub 2019 Dec 4.

DOI:10.1021/acs.bioconjchem.9b00653
PMID:31765569
Abstract

Sonothrombolysis with microbubbles can enhance the dissolution of thrombus through the cavitation effect of microbubbles under ultrasound irradiation. However, the detailed mechanism of thrombolysis with microscaled or nanoscaled bubbles is still not so clear. This study compared the thrombolytic capacity of cRGD-targeted or nontargeted bubbles with different particle sizes combined with urokinase (UK). The size of the microscaled bubbles (Mbs or Mbs-cRGD) was mostly approximately 3 μm, while the nanoscaled bubbles (Nbs or Nbs-cRGD) were mainly around 220 nm. testing was performed on an extracorporeal circulation device that mimics human vascular thromboembolism. The rabbit clots in Mbs with UK groups showed peripheral worm-like dissolution, while the clots in Nbs with UK groups showed internal fissure-like collapse. In addition, the thrombolysis rate of Nbs-cRGD with the UK group was the highest. Furthermore, the scanning electron microscopic images showed that the fibrin network was the most severely damaged by the Nbs-cRGD, and most of the fibrin strands were dissolved. Especially, the Nbs-cRGD can penetrate much deeper than Mbs-cRGD into the thrombus and loosen the fibrin network. Taken together, benefiting from the specific identification and deep penetration to thrombus, our developed novel targeted Nbs may have broad application prospects in the clinic.

摘要

超声辐射下微泡的声空化效应可增强血栓的溶解。然而,微泡和纳泡在溶栓方面的详细机制仍不清楚。本研究对比了载靶向或非靶向配体的不同粒径的微泡和纳泡联合尿激酶(UK)的溶栓能力。微泡(Mbs 或 Mbs-cRGD)的粒径主要约为 3μm,而纳泡(Nbs 或 Nbs-cRGD)主要约为 220nm。通过模拟人体血管血栓栓塞的体外循环装置进行检测。载 UK 的 Mbs 组中的兔血栓显示出周边虫状溶解,而载 UK 的 Nbs 组中的血栓显示出内部裂隙状塌陷。此外,载 UK 的 Nbs-cRGD 组的溶栓率最高。此外,扫描电子显微镜图像显示,Nbs-cRGD 对纤维蛋白网络的破坏最严重,大部分纤维蛋白链溶解。特别是,Nbs-cRGD 比 Mbs-cRGD 能更深地渗透到血栓中,并疏松纤维蛋白网络。综上所述,由于具有特异性识别和深层渗透到血栓的特性,我们开发的新型靶向 Nbs 可能具有广阔的临床应用前景。

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