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靶向微泡在调制声辐射力作用下的结合动力学。

Binding dynamics of targeted microbubbles in response to modulated acoustic radiation force.

机构信息

Department of Biomedical Engineering, University of Virginia, Charlottesville, VA 22908, USA.

出版信息

Phys Med Biol. 2014 Jan 20;59(2):465-84. doi: 10.1088/0031-9155/59/2/465. Epub 2013 Dec 30.

DOI:10.1088/0031-9155/59/2/465
PMID:24374866
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4068277/
Abstract

Detection of molecular targeted microbubbles plays a foundational role in ultrasound-based molecular imaging and targeted gene or drug delivery. In this paper, an empirical model describing the binding dynamics of targeted microbubbles in response to modulated acoustic radiation forces in large vessels is presented and experimentally verified using tissue-mimicking flow phantoms. Higher flow velocity and microbubble concentration led to faster detaching rates for specifically bound microbubbles (p < 0.001). Higher time-averaged acoustic radiation force intensity led to faster attaching rates and a higher saturation level of specifically bound microbubbles (p < 0.05). The level of residual microbubble signal in targeted experiments after cessation of radiation forces was the only response parameter that was reliably different between targeted and control experiments (p < 0.05). A related parameter, the ratio of residual-to-saturated microbubble signal (Rresid), is proposed as a measurement that is independent of absolute acoustic signal magnitude and therefore able to reliably detect targeted adhesion independently of control measurements (p < 0.01). These findings suggest the possibility of enhanced detection of specifically bound microbubbles in real-time, using relatively short imaging protocols (approximately 3 min), without waiting for free microbubble clearance.

摘要

检测分子靶向微泡在基于超声的分子成像和靶向基因或药物传递中起着基础作用。本文提出了一种经验模型,描述了在大血管中调制声辐射力作用下靶向微泡的结合动力学,并使用组织模拟流动体模进行了实验验证。较高的流速和微泡浓度导致特异性结合的微泡更快地脱离(p<0.001)。较高的时均声辐射力强度导致更快的附着率和更高的特异性结合微泡的饱和水平(p<0.05)。在停止辐射力后,靶向实验中剩余的微泡信号水平是靶向和对照实验之间唯一可靠不同的响应参数(p<0.05)。提出了一个相关参数,即剩余至饱和微泡信号的比值(Rresid),作为一种测量方法,它不依赖于绝对声信号幅度,因此能够可靠地检测靶向粘附,而无需对照测量(p<0.01)。这些发现表明,有可能在实时检测中增强特异性结合的微泡,使用相对较短的成像协议(约 3 分钟),而无需等待游离微泡清除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/1c766ab1e828/nihms553785f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/0b2b6e1c01ff/nihms553785f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/7b76a42902ab/nihms553785f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/1a6034a28d9c/nihms553785f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/e457749cb9bd/nihms553785f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/da08b022ec81/nihms553785f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/f2c8ec4339cc/nihms553785f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/fcf0ba531e5a/nihms553785f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/a878e857ed30/nihms553785f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/1c766ab1e828/nihms553785f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/0b2b6e1c01ff/nihms553785f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/7b76a42902ab/nihms553785f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/1a6034a28d9c/nihms553785f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/e457749cb9bd/nihms553785f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/da08b022ec81/nihms553785f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/f2c8ec4339cc/nihms553785f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/fcf0ba531e5a/nihms553785f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/a878e857ed30/nihms553785f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f4/4068277/1c766ab1e828/nihms553785f9.jpg

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