Department of Neurosurgery, University of Marburg, Marburg, Germany.
Eur J Pharm Biopharm. 2011 Apr;77(3):424-9. doi: 10.1016/j.ejpb.2010.12.003. Epub 2010 Dec 17.
In the present study, we investigated the sonothrombolytic effect of new nanoscaled lipid formulations in human blood clots, using diagnostic ultrasound. Human blood clots of 1 ml were incubated with 1 μl of the different lipid dispersions DPPC/CH, DPPC/PEG40S, DSPC/PEG40S and the commercially available ultrasound contrast agent SonoVue®. Clots were stored for 3 days at 5 °C to obtain maximal clot retraction and lytic resistance. Each clot weight was determined before and after continuous insonation for 1h of insonation at 1.4 MHz. The pressure in the insonation chamber was 80 mm Hg to mimic middle arterial blood pressure. There were no significant differences in thrombus weight before insonation. All nanoscaled formulations and SonoVue® were able to reduce thrombus weight compared to the weight loss of clots that were not insonated but kept under pressure for one hour (p < 0.001). We found a highly significant weight reduction with DSPC/PEG40S compared to SonoVue® (p = 0.007). Nanoscaled DSPC/PEG40S dispersion could be a promising formulation in ultrasound enhanced thrombolysis even without thrombolytic drugs. Stable cavitation is a crucial parameter in fragmentation of thrombus architecture. Further studies of physicochemical properties of DSPC/PEG40S are necessary to corroborate our hypothesis.
在本研究中,我们使用诊断超声研究了新型纳米级脂质制剂在人血凝块中的超声溶栓作用。将 1ml 人血凝块与 1μl 不同脂质分散体 DPPC/CH、DPPC/PEG40S、DSPC/PEG40S 和市售超声造影剂 SonoVue®孵育。将凝块在 5°C 下储存 3 天以获得最大的凝块回缩和溶栓抵抗。在 1.4MHz 下连续照射 1 小时之前和之后,每个凝块的重量都进行了测定。声腔中的压力为 80mmHg,以模拟中动脉血压。在照射前,血栓的重量没有明显差异。与未照射但保持压力 1 小时的血栓相比,所有纳米制剂和 SonoVue®均能降低血栓重量(p<0.001)。与 SonoVue®相比,DSPC/PEG40S 具有显著的重量减轻(p=0.007)。即使没有溶栓药物,纳米级 DSPC/PEG40S 分散体也可能成为超声增强溶栓的有前途的制剂。稳定空化是血栓结构碎裂的关键参数。需要进一步研究 DSPC/PEG40S 的物理化学性质来证实我们的假设。