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治疗性超声造影剂的动力学

Dynamics of therapeutic ultrasound contrast agents.

作者信息

Allen John S, May Donovan J, Ferrara Katherine W

机构信息

Department of Biomedical Engineering, University of California at Davis, Davis, CA 95616, USA.

出版信息

Ultrasound Med Biol. 2002 Jun;28(6):805-16. doi: 10.1016/s0301-5629(02)00522-7.

Abstract

Novel therapeutic contrast agents offer great potential for localized drug delivery. Localized delivery should significantly improve the efficacy of drug delivery and reduce any toxic exposure to the healthy tissue. This work describes a preliminary theoretical description of agents, such as those developed by the ImaRx Corporation, enclosed by a relatively thick fluid shell. A theoretical extension is made to a generalized Rayleigh-Plesset formulation that allows it to be solved for an encapsulating liquid shell of arbitrary thickness and density. The equation is used to investigate the role of shell thickness, density and viscosity on the radial dynamics and velocity of the inner and outer radii. Comparisons are made with experimental measurements of the maximum radial expansions for agents with triacetin shells. For a seven-cycle driving acoustic pulse with a center frequency of 1.5 MHz and peak amplitude of 1.6 MPa, the equation predicts maximum expansions from 5.5 to 1.3 times the initial radius for agents 1 to 10 microm, respectively, in initial radius with a 500-nm (28.0 cP) encapsulating shell. These predictions have reasonable agreement with the maximum radial expansions obtained from optical experimental data of fragmenting and intact agents. Approximate agreement between theory and experiment for a similar range of agent sizes is also demonstrated for a pulse with the same pressure amplitude at 2.5 MHz. At 2.5 MHz, smaller radial expansion amplitudes from 1.1 to 4.1 times the initial radius were found for agents 1 to 10 microm in initial radius, respectively. Discrepancies are attributed to shape instabilities and their associated fragmentation effects not incorporated in the equation. A significant difference in the inner and outer wall velocities is predicted for agents with a 500-nm triacetin shell. A 2.5 microm initial radius agent driven with a seven-cycle pulse at 2.5 MHz and 1.6 MPa achieves a maximum negative inner wall velocity of 364 m/s and outer wall velocity of 63 m/s. For parameters that correspond to large differences between the inner and outer wall velocities, fragmentation is typically observed experimentally.

摘要

新型治疗性造影剂在局部药物递送方面具有巨大潜力。局部递送应能显著提高药物递送的疗效,并减少对健康组织的任何毒性暴露。这项工作描述了对诸如ImaRx公司研发的被相对较厚的流体壳包裹的造影剂的初步理论描述。对广义瑞利 - 普莱斯方程进行了理论扩展,使其能够求解任意厚度和密度的包裹液壳。该方程用于研究壳厚度、密度和粘度对内外半径的径向动力学和速度的作用。将其与具有三醋精壳的造影剂的最大径向膨胀的实验测量结果进行了比较。对于中心频率为1.5 MHz、峰值幅度为1.6 MPa的七周期驱动声脉冲,该方程预测,对于初始半径为1至10微米、包裹壳厚度为500纳米(粘度为28.0厘泊)的造影剂,最大膨胀分别为初始半径的5.5至1.3倍。这些预测与从破碎和完整造影剂的光学实验数据获得的最大径向膨胀有合理的一致性。对于在2.5 MHz具有相同压力幅度的脉冲,在类似大小的造影剂范围内,理论与实验也显示出近似的一致性。在2.5 MHz时,初始半径为1至10微米的造影剂的径向膨胀幅度较小,分别为初始半径的1.1至4.1倍。差异归因于方程中未纳入的形状不稳定性及其相关的破碎效应。对于具有500纳米三醋精壳的造影剂,预测其内壁和外壁速度存在显著差异。一个初始半径为2.5微米的造影剂在2.5 MHz和1.6 MPa下由七周期脉冲驱动时,内壁最大负速度达到364 m/s,外壁速度为63 m/s。对于对应于内壁和外壁速度有较大差异的参数,实验中通常会观察到破碎现象。

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