Lea-Banks Harriet, Teo Boon, Stride Eleanor, Coussios Constantin C
Phys Med Biol. 2016 Nov 21;61(22):7906-7918. doi: 10.1088/0031-9155/61/22/7906. Epub 2016 Oct 25.
A significant barrier to successful drug delivery is the limited penetration of nanoscale therapeutics beyond the vasculature. Building on recent in vivo findings in the context of cancer drug delivery, the current study investigates whether modification of nanoparticle drug-carriers to increase their density can be used to enhance their penetration into viscoelastic materials under ultrasound exposure. A computational model is first presented to predict the transport of identically sized nanoparticles of different densities in an ultrasonic field in the presence of an oscillating microbubble, by a combination of primary and secondary acoustic radiation forces, acoustic streaming and microstreaming. Experiments are then described in which near monodisperse (polydispersity index <0.2) nanoparticles of approximate mean diameter 200 nm and densities ranging from 1.01 g cm to 5.58 g cm were fabricated and delivered to a tissue-mimicking material in the presence or absence of a microbubble ultrasound contrast agent, at ultrasound frequencies of 0.5 MHz and 1.6 MHz and a peak negative pressure of 1 MPa. Both the theoretical and experimental results confirm that denser particles exhibit significantly greater ultrasound-mediated transport than their lower density counterparts, indicating that density is a key consideration in the design of nanoscale therapeutics.
成功进行药物递送的一个重大障碍是纳米级治疗剂在脉管系统之外的穿透能力有限。基于近期在癌症药物递送背景下的体内研究结果,本研究调查了对纳米颗粒药物载体进行改性以增加其密度,是否可用于在超声照射下增强其对粘弹性材料的穿透能力。首先提出了一个计算模型,通过初级和次级声辐射力、声流和微流的组合,预测在存在振荡微泡的超声场中不同密度的相同尺寸纳米颗粒的传输。然后描述了实验,其中制备了平均直径约为200nm、密度范围为1.01g/cm至5.58g/cm的近单分散(多分散指数<0.2)纳米颗粒,并在有或没有微泡超声造影剂的情况下,以0.5MHz和1.6MHz的超声频率以及1MPa的峰值负压递送至组织模拟材料中。理论和实验结果均证实,密度较大的颗粒比密度较低的颗粒表现出明显更大的超声介导传输,这表明密度是纳米级治疗剂设计中的一个关键考虑因素。