Faculty of Engineering and Physical Sciences, Department of Mechanical Engineering, University of Southampton, UK; Centre for Human Development, Stem Cells and Regeneration, Bioengineering Sciences, Faculty of Medicine, University of Southampton, UK; Institute for Life Sciences (IfLS), University of Southampton, UK.
Department of Engineering Science, University of Oxford, UK.
Ultrason Sonochem. 2021 May;73:105482. doi: 10.1016/j.ultsonch.2021.105482. Epub 2021 Feb 3.
Liquid perfluorocarbon nanodroplets (NDs) are an attractive alternative to microbubbles (MBs) for ultrasound-mediated therapeutic and diagnostic applications. ND size and size distribution have a strong influence on their behaviour in vivo, including extravasation efficiency, circulation time, and response to ultrasound stimulation. Thus, it is desirable to identify ways to tailor the ND size and size distribution during manufacturing. In this study phospholipid-coated NDs, comprising a perfluoro-n-pentane (PFP) core stabilised by a DSPC/PEG40s (1,2-distearoyl-sn-glycero-3-phosphocholine and polyoxyethylene(40)stearate, 9:1 molar ratio) shell, were produced in phosphate-buffered saline (PBS) by sonication. The effect of the following production-related parameters on ND size was investigated: PFP concentration, power and duration of sonication, and incorporation of a lipophilic fluorescent dye. ND stability was also assessed at both 4 °C and 37 °C. When a sonication pulse of 6 s and 15% duty cycle was employed, increasing the volumetric concentration of PFP from 5% to 15% v/v in PBS resulted in an increase in ND diameter from 215.8 ± 16.8 nm to 408.9 ± 171.2 nm. An increase in the intensity of sonication from 48 to 72 W (with 10% PFP v/v in PBS) led to a decrease in ND size from 354.6 ± 127.2 nm to 315.0 ± 100.5 nm. Increasing the sonication time from 20 s to 40 s (using a pulsed sonication with 30% duty cycle) did not result in a significant change in ND size (in the range 278-314 nm); however, when it was increased to 60 s, the average ND diameter reduced to 249.7 ± 9.7 nm, which also presented a significantly lower standard deviation compared to the other experimental conditions investigated (i.e., 9.7 nm vs. > 49.4 nm). The addition of the fluorescent dye DiI at different molar ratios did not affect the ND size distribution. NDs were stable at 4 °C for up to 6 days and at 37 °C for up to 110 min; however, some evidence of ND-to-MB phase transition was observed after 40 min at 37 °C. Finally, phase transition of NDs into MBs was demonstrated using a tissue-mimicking flow phantom under therapeutic ultrasound exposure conditions (ultrasound frequency: 0.5 MHz, acoustic pressure: 2-4 MPa, and pulse repetition frequency: 100 Hz).
液态全氟碳纳米液滴(NDs)是一种有吸引力的替代微泡(MBs)的选择,可用于超声介导的治疗和诊断应用。ND 的大小和分布对其在体内的行为有很强的影响,包括外渗效率、循环时间和对超声刺激的反应。因此,希望找到在制造过程中调整 ND 大小和分布的方法。在这项研究中,采用声振法在磷酸盐缓冲盐水(PBS)中制备了由全氟正戊烷(PFP)核和 DSPC/PEG40s(1,2-二硬脂酰-sn-甘油-3-磷酸胆碱和聚氧乙烯(40)硬脂酸,9:1 摩尔比)壳稳定的磷脂包覆的 NDs。研究了以下与生产相关的参数对 ND 大小的影响:PFP 浓度、声振功率和时间以及脂溶性荧光染料的掺入。还在 4°C 和 37°C 下评估了 ND 的稳定性。当使用 6 s 的声振脉冲和 15%的占空比时,PBS 中 PFP 体积浓度从 5%增加到 15%,导致 ND 直径从 215.8±16.8nm 增加到 408.9±171.2nm。声振强度从 48 W 增加到 72 W(PBS 中 10%PFP v/v),导致 ND 尺寸从 354.6±127.2nm 减小到 315.0±100.5nm。将声振时间从 20 s 增加到 40 s(使用 30%占空比的脉冲声振)不会导致 ND 尺寸发生显著变化(范围为 278-314nm);然而,当增加到 60 s 时,平均 ND 直径减小到 249.7±9.7nm,与研究的其他实验条件相比,标准偏差也显著降低(即 9.7nm 与>49.4nm)。以不同摩尔比添加荧光染料 DiI 不会影响 ND 大小分布。ND 在 4°C 下可稳定保存长达 6 天,在 37°C 下可稳定保存长达 110 分钟;然而,在 37°C 下 40 分钟后观察到 ND 向 MB 相转变的一些证据。最后,在治疗超声暴露条件下(超声频率:0.5MHz,声压:2-4MPa,脉冲重复频率:100Hz),使用组织模拟流动体模证明了 ND 向 MB 的相变。