Joint Department of Biomedical Engineering, University of North Carolina and North Carolina State University, Chapel Hill, North Carolina 27599, USA.
Langmuir. 2011 Sep 6;27(17):10412-20. doi: 10.1021/la2013705. Epub 2011 Jul 28.
Recent efforts in the area of acoustic droplet vaporization with the objective of designing extravascular ultrasound contrast agents has led to the development of stabilized, lipid-encapsulated nanodroplets of the highly volatile compound decafluorobutane (DFB). We developed two methods of generating DFB droplets, the first of which involves condensing DFB gas (boiling point from -1.1 to -2 °C) followed by extrusion with a lipid formulation in HEPES buffer. Acoustic droplet vaporization of micrometer-sized lipid-coated droplets at diagnostic ultrasound frequencies and mechanical indices were confirmed optically. In our second formulation methodology, we demonstrate the formulation of submicrometer-sized lipid-coated nanodroplets based upon condensation of preformed microbubbles containing DFB. The droplets are routinely in the 200-300 nm range and yield microbubbles on the order of 1-5 μm once vaporized, consistent with ideal gas law expansion predictions. The simple and effective nature of this methodology allows for the development of a variety of different formulations that can be used for imaging, drug and gene delivery, and therapy. This study is the first to our knowledge to demonstrate both a method of generating ADV agents by microbubble condensation and formulation of primarily submicrometer droplets of decafluorobutane that remain stable at physiological temperatures. Finally, activation of DFB nanodroplets is demonstrated using pressures within the FDA guidelines for diagnostic imaging, which may minimize the potential for bioeffects in humans. This methodology offers a new means of developing extravascular contrast agents for diagnostic and therapeutic applications.
近年来,人们致力于研究声学空化作用,旨在设计血管外超声对比剂,从而推动了具有挥发性的全氟丁烷(DFB)的稳定脂包纳米液滴的发展。我们开发了两种生成 DFB 液滴的方法,第一种方法涉及 DFB 气体的冷凝(沸点为-1.1 至-2°C),然后与 HEPES 缓冲液中的脂质制剂一起挤压。在诊断超声频率和机械指数下,对微米级脂质包裹液滴的声致空化作用进行了光学确认。在我们的第二种配方方法中,我们展示了基于含有 DFB 的预形成微泡的冷凝来制备亚微米级脂质包裹纳米液滴的方法。这些液滴通常在 200-300nm 范围内,一旦蒸发,就会产生 1-5μm 的微泡,这与理想气体定律的膨胀预测一致。这种方法简单有效,允许开发各种不同的制剂,可用于成像、药物和基因传递以及治疗。据我们所知,这项研究首次证明了一种通过微泡冷凝生成 ADV 试剂的方法,并证明了主要由亚微米级 DFB 液滴组成的制剂在生理温度下保持稳定。最后,使用符合 FDA 诊断成像指南的压力来证明 DFB 纳米液滴的激活,这可能会最大限度地减少对人体产生生物效应的潜在风险。这种方法为开发用于诊断和治疗应用的血管外对比剂提供了一种新手段。