School of Mechanical and Mining Engineering, University of Queensland, Brisbane, Australia.
School of Pharmacy, University of Queensland, Brisbane, Australia.
Phys Eng Sci Med. 2021 Mar;44(1):79-91. doi: 10.1007/s13246-020-00954-4. Epub 2021 Jan 4.
This paper investigates the shell elastic properties and the number-concentration stability of a new acoustofluidic delivery agent liposome in comparison to Definity™, a monolayer ultrasonic contrast agent microbubble. The frequency dependent attenuation of an acoustic beam passing through a microbubble suspension was measured to estimate the shell parameters. The excitation voltage was adjusted to ensure constant acoustic pressure at all frequencies. The pressure was kept at the lowest possible magnitude to ensure that effects from nonlinear bubble behaviour which are not considered in the analytical model were minimal. The acoustofluidic delivery agent shell stiffness S and friction S parameters were determined as (S = 0.11 N/m, S = 0.31 × 10 Kg/s at 25 °C) in comparison to the Definity™ monolayer ultrasound contrast agent which were (S = 1.53 N/m, S = 1.51 × 10 Kg/s at 25 °C). When the temperature was raised to physiological levels, the friction coefficient S decreased by 28% for the monolayer microbubbles and by only 9% for the liposomes. The stiffness parameter S of the monolayer microbubble decreased by 23% while the stiffness parameter of the liposome increased by a similar margin (27%) when the temperature was raised to 37 °C. The size distribution of the bubbles was measured using Tunable Resistive Pulse Sensing (TRPS) for freshly prepared microbubbles and for bubble solutions at 6 h and 24 h after activation to investigate their number-concentration stability profile. The liposome maintained >80% of their number-concentration for 24 h at physiological temperature, while the monolayer microbubbles maintained only 27% of their number-concentration over the same period. These results are important input parameters for the design of effective acoustofluidic delivery systems using the new liposomes.
本文研究了一种新的声流控递送试剂脂质体的壳弹性特性和浓度稳定性,与单层超声造影剂微泡 Definity™进行了比较。通过测量穿过微泡悬浮液的声束的频率依赖性衰减来估计壳参数。调整激励电压以确保在所有频率下都保持恒定的声压。将压力保持在尽可能低的水平,以确保不会出现分析模型中未考虑的非线性气泡行为的影响。与 Definity™单层超声造影剂相比,声流控递送试剂的壳硬度 S 和摩擦 S 参数分别为(S = 0.11 N/m,S = 0.31×10 Kg/s 在 25°C),而 Definity™单层超声造影剂的壳硬度 S 和摩擦 S 参数分别为(S = 1.53 N/m,S = 1.51×10 Kg/s 在 25°C)。当温度升高到生理水平时,单层微泡的摩擦系数 S 降低了 28%,而脂质体仅降低了 9%。当温度升高到 37°C 时,单层微泡的刚度参数 S 降低了 23%,而脂质体的刚度参数增加了相似的幅度(27%)。使用可调电阻脉冲传感(TRPS)测量新制备的微泡和激活后 6 小时和 24 小时的微泡溶液的气泡尺寸分布,以研究其浓度稳定性。脂质体在生理温度下保持 >80%的浓度 24 小时,而单层微泡在相同时间内仅保持 27%的浓度。这些结果是使用新脂质体设计有效声流控递送系统的重要输入参数。