4.8 Article

Characterization of the interaction of nanobubble ultrasound contrast agents with human blood components

期刊

BIOACTIVE MATERIALS
卷 19, 期 -, 页码 642-652

出版社

KEAI PUBLISHING LTD
DOI: 10.1016/j.bioactmat.2022.05.001

关键词

Nanobubbles; Ultrasound contrast agents; Red blood cells; Hitchhiking; Ultrasound; Drug delivery

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This study examined the effects of blood components on the acoustic response of nanobubbles. The results showed that nanobubbles in human whole blood had a gradual increase in signal enhancement and attached to the surface of red blood cells, indicating that direct interaction between nanobubbles and red blood cells may be key to extending their circulation time.
Nanoscale ultrasound contrast agents, or nanobubbles, are being explored in preclinical applications ranging from vascular and cardiac imaging to targeted drug delivery in cancer. These sub-micron particles are approximately 10x smaller than clinically available microbubbles. This allows them to effectively traverse compromised physiological barriers and circulate for extended periods of time. While various aspects of nanobubble behavior have been previously examined, their behavior in human whole blood has not yet been explored. Accordingly, herein we examined, for the first time, the short and long-term effects of blood components on nanobubble acoustic response. We observed differences in the kinetics of backscatter from nanobubble suspensions in whole blood compared to bubbles in phosphate buffered saline (PBS), plasma, or red blood cell solutions (RBCs). Specifically, after introducing nanobubbles to fresh human whole blood, signal enhancement, or the magnitude of nonlinear ultrasound signal, gradually increased by 22.8 +/- 13.1% throughout our experiment, with peak intensity reached within 145 s. In contrast, nanobubbles in PBS had a stable signal with negligible change in intensity (-1.7 +/- 3.2%) over 8 min. Under the same conditions, microbubbles made with the same lipid formulation showed a -56.8 +/- 6.1% decrease in enhancement in whole blood. Subsequent confocal, fluorescent, and scanning electron microscopy analysis revealed attachment of the nanobubbles to the surface of RBCs, suggesting that direct interactions, or hitchhiking, of nanobubbles on RBCs in the presence of plasma may be a possible mechanism for the observed effects. This phenomenon could be key to extending nanobubble circulation time and has broad implications in drug delivery, where RBC interaction with nanoparticles could be exploited to improve delivery efficiency.

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