Wallace N, Wrenn S P
Department of Chemical Engineering, Drexel University, 3141 Chestnut St, Philadelphia, PA 19104, United States.
Ultrasonics. 2015 Dec;63:31-8. doi: 10.1016/j.ultras.2015.06.006. Epub 2015 Jun 28.
When ultrasound contrast agent microbubbles are nested within a liposome, damage to the liposome membrane caused by both stable and inertial cavitation of the microbubble allows for release of the aqueous core of the liposome. Triggered release was not accomplished unless microbubbles were present within the liposome. Leakage was tested using fluorescence assays developed specifically for this drug delivery vehicle and qualitative measurements using an optical microscope. These studies were done using a 1 MHz focused ultrasound transducer while varying parameters including peak negative ultrasound pressure, average liposome diameter, and microbubble concentration. Two regimes exist for membrane disruption caused by cavitating microbubbles. A faster release rate, as well as permanent membrane damage are seen for samples exposed to high pressure (2.1-3.7 MPa). A slower release rate and dilation/temporary poration are characteristic of stable cavitation for low pressure studies (0.54-1.7 MPa).
当超声造影剂微泡包裹于脂质体内时,微泡的稳态空化和惯性空化对脂质体膜造成的损伤会使脂质体水相内核得以释放。只有脂质体内存在微泡时,才能实现触发释放。渗漏情况通过专门为此药物递送载体开发的荧光测定法以及使用光学显微镜进行的定性测量来检测。这些研究使用1兆赫聚焦超声换能器进行,同时改变包括负向超声峰值压力、脂质体平均直径和微泡浓度等参数。空化微泡导致膜破坏存在两种情况。暴露于高压(2.1 - 3.7兆帕)的样品呈现出更快的释放速率以及永久性膜损伤。对于低压研究(0.54 - 1.7兆帕),较慢的释放速率以及扩张/暂时成孔是空化稳态的特征。