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声辐射力增强超声造影微泡的靶向递送:体外验证

Acoustic radiation force enhances targeted delivery of ultrasound contrast microbubbles: in vitro verification.

作者信息

Rychak Joshua J, Klibanov Alexander L, Hossack John A

机构信息

University of Virginia, Charlottesville, VA 22904, USA.

出版信息

IEEE Trans Ultrason Ferroelectr Freq Control. 2005 Mar;52(3):421-33. doi: 10.1109/tuffc.2005.1417264.

Abstract

Recent research has shown that targeted ultrasound contrast microbubbles achieve specific adhesion to regions of intravascular pathology, but not in areas of high flow. It has been suggested that acoustic radiation can be used to force free-stream microbubbles toward the target, but this has not been verified for actual targeted contrast agents. We present evidence that acoustic radiation indeed increases the specific targeted accumulation of microbubbles. Lipid microbubbles bearing an antibody as a targeting ligand were infused through a microcapillary flow chamber coated with P-selectin as the target protein. A 2.0 MHz ultrasonic pulse was applied perpendicular to the flow direction. Microbubble accumulation was observed on the flow chamber surface opposite the transducer. An acoustic pressure of 122 kPa enhanced microbubble adhesion up to 60-fold in a microbubble concentration range of 0.25 x 10(6) to 75 x 106) ml(-1). Acoustic pressure mediated the greatest adhesion enhancement at concentrations within the clinical dosing range. Acoustic pressure enhanced targeting nearly 80-fold at a wall shear rate of 1244 s(-1), suggesting that this mechanism is appropriate for achieving targeted microbubble delivery in high-flow vessels. Microbubble adhesion increased with the square of acoustic pressure between 25 and 122 kPa, and decreased substantially at higher pressures.

摘要

最近的研究表明,靶向超声造影微泡可实现对血管内病变区域的特异性黏附,但在高血流区域则不然。有人提出可以利用声辐射将自由流动的微泡推向目标,但这一点尚未在实际的靶向造影剂中得到验证。我们提供的证据表明,声辐射确实会增加微泡的特异性靶向聚集。将带有作为靶向配体的抗体的脂质微泡通过涂有作为靶蛋白的P-选择素的微毛细管流动腔注入。施加一个2.0 MHz的超声脉冲,使其垂直于流动方向。在换能器对面的流动腔表面观察到微泡聚集。在0.25×10⁶至75×10⁶个/毫升的微泡浓度范围内,122 kPa的声压可使微泡黏附增强高达60倍。在临床给药范围内的浓度下,声压介导的黏附增强作用最大。在壁面剪切速率为1244 s⁻¹时,声压使靶向作用增强近80倍,这表明该机制适用于在高血流血管中实现靶向微泡递送。在25至122 kPa之间,微泡黏附随声压的平方增加,而在更高压力下则大幅下降。

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