Measuring the effects of ultrasound on contrast agents

S. Podell, Brent Golec, Rolf Lohnnann
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引用次数: 2

Abstract

In vitro acoustic studies generally assume that known and reproducible quantities of contrast media are being evaluated, without need for agent retesting after dilution and handling. This assumption is incorrect, because duration of ultrasound contrast is substantially reduced by dilution of encapsulated, gas-filled agents into gas-poor solutions. Contrast agent persistence is enhanced and diffusive gas loss is slowed, but not eliminated, by filling microspheres with core gases having lower aqueous solubility. Since diffusive gas loss promotes safe elimination of gas bubbles in vivo, it is a desirable property that may prove unavoidable for commercial contrast agents. For non-encapsulated contrast agents containing emulsified perfluorocarbon liquids, exposure to threshold levels of ultrasound energy increased the dose of available contrast, by causing superheated liquid droplets to boil and form new microbubbles. This sudden activation threshold was not observed in encapsulated microsphere formulations, where the same perfluorocarbon was converted to vapor phase prior to insonation. These findings show that effective contrast agent doses can rapidly increase or decrease under conditions commonly used for in vitro acoustic testing. To avoid potential misinterpretation of experimental results, the effects of ultrasound independent factors on contrast agent stability need to be carefully considered.
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测量超声对造影剂的影响
体外声学研究通常假设正在评估已知和可重复数量的造影剂,不需要在稀释和处理后重新测试造影剂。这种假设是不正确的,因为将封装的充气剂稀释到无气溶液中,超声造影剂的持续时间大大缩短。用溶解度较低的核心气体填充微球,可以增强造影剂的持久性,减缓弥漫性气体的损失,但不能消除。由于弥漫性气体损失促进了体内气泡的安全消除,这是一种理想的特性,对于商业造影剂来说可能是不可避免的。对于含有乳化全氟碳液体的非封装造影剂,暴露在超声能量阈值水平下会导致过热的液滴沸腾并形成新的微泡,从而增加可用造影剂的剂量。在封装的微球配方中没有观察到这种突然的激活阈值,在这种配方中,相同的全氟碳化合物在照射前转化为气相。这些发现表明,在通常用于体外声学测试的条件下,有效造影剂剂量可以迅速增加或减少。为了避免对实验结果的误读,需要仔细考虑超声无关因素对造影剂稳定性的影响。
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