Zhang Hongyi, Lu Chang, Yu Alfred C H, Qin Peng
School of Automation and Intelligent Sensing, Shanghai Jiao Tong University, Shanghai 200240, China.
Schlegel Research Institute for Aging, University of Waterloo, Waterloo, ON N2L3G1, Canada.
Acta Biomater. 2025 Sep 15;204:596-609. doi: 10.1016/j.actbio.2025.08.017. Epub 2025 Aug 8.
The stability and acoustic-induced oscillation of microbubbles strongly depend on their shell properties. Determining the relationships between the shell composition and bubble stability and shell elasticity is crucial for improving microbubble-based ultrasound imaging and therapy. We used a flow-focusing microfluidic to fabricate monodisperse microbubbles with a primary lipid and pegylated-lipid at different molar ratios. The lipid density on the shell was regulated via the ambient pressure. The measured pressure-dependent resonance-frequency curve was used to characterize bubble states (i.e., elasticity, rupture, buckling, elastic-rupture transition, and elastic-buckling transition). Further, by tracking pressure-dependent resonance-frequency curves over time during dissolution, the rate of bubble dissolution (i.e., stability) was quantified. The surface-area-dependent elasticity was obtained by fitting the bubble oscillation model to the measured pressure-dependent attenuation spectra. With decreasing molar fraction of pegylated-lipid, the evolution rate of microbubbles from the elasticity to elastic-buckling regimes gradually increased, corresponding to a decrease in stability of microbubbles. Upon bubble expansion, the elasticity first peaked, then decreased to the elasticity-rupture transition point, followed by a quick decrease to the rupture regime. Upon bubble compression, the elasticity plateaued until the elastic-buckling transition point, and then rapidly declined to the buckling regime. Significantly lower elasticity was found in microbubbles with 5 %-10 % pegylated-lipid than those with 1 % and 2 %; above and below 5 %, the molar fraction did not affect the elasticity. This work represents a reliable and accurate approach to understand the bubble stability and shell viscoelastic mechanisms, and to tailor phospholipids for microbubble-based medical applications. STATEMENT OF SIGNIFICANCE: Determining the relationships between shell composition, bubble stability and shell elasticity is critical for designing state-of-art microbubbles and improving ultrasound-based imaging and therapy. The pressure-dependent resonance-frequency curves over time was used to characterize monodisperse microbubble states (i.e., elasticity, rupture, buckling, elastic-rupture transition, and elastic-buckling transition) and to quantify the bubble dissolution rate (i.e., stability). With decreasing pegylated-lipid content on the shell, the bubble dissolution rate increased while stability decreased. Additionally, the pressure-dependent attenuation spectra were used to characterize nonlinear surface-area-dependent elasticity. The chain configurations (e.g., mushroom or brush) of pegylated-lipid dominated shell elasticity. This work deepens the understanding of viscoelastic mechanisms of bubble shell, and provides a systematic approach to tailor shell compositions for optimized microbubble-based medical applications.
微泡的稳定性和声致振荡强烈依赖于其壳层特性。确定壳层组成与气泡稳定性及壳层弹性之间的关系对于改进基于微泡的超声成像和治疗至关重要。我们使用流动聚焦微流体技术制备了具有不同摩尔比的主要脂质和聚乙二醇化脂质的单分散微泡。壳层上的脂质密度通过环境压力进行调节。测量的压力依赖性共振频率曲线用于表征气泡状态(即弹性、破裂、屈曲、弹性 - 破裂转变和弹性 - 屈曲转变)。此外,通过在溶解过程中随时间跟踪压力依赖性共振频率曲线,对气泡溶解速率(即稳定性)进行了量化。通过将气泡振荡模型拟合到测量的压力依赖性衰减光谱来获得表面积依赖性弹性。随着聚乙二醇化脂质摩尔分数的降低,微泡从弹性状态到弹性 - 屈曲状态的演化速率逐渐增加,这对应于微泡稳定性的降低。在气泡膨胀时,弹性首先达到峰值,然后降至弹性 - 破裂转变点,随后迅速降至破裂状态。在气泡压缩时,弹性保持平稳直至弹性 - 屈曲转变点,然后迅速下降至屈曲状态。发现聚乙二醇化脂质含量为5% - 10%的微泡的弹性明显低于含量为1%和2%的微泡;在5%之上和之下,摩尔分数不影响弹性。这项工作代表了一种可靠且准确的方法,用于理解气泡稳定性和壳层粘弹性机制,并为基于微泡的医学应用定制磷脂。重要性声明:确定壳层组成、气泡稳定性和壳层弹性之间的关系对于设计先进的微泡以及改进基于超声的成像和治疗至关重要。随时间变化的压力依赖性共振频率曲线用于表征单分散微泡状态(即弹性、破裂、屈曲、弹性 - 破裂转变和弹性 - 屈曲转变)并量化气泡溶解速率(即稳定性)。随着壳层上聚乙二醇化脂质含量的降低,气泡溶解速率增加而稳定性降低。此外,压力依赖性衰减光谱用于表征非线性表面积依赖性弹性。聚乙二醇化脂质的链构型(例如蘑菇状或刷状)主导壳层弹性。这项工作加深了对气泡壳层粘弹性机制的理解,并提供了一种系统方法来定制壳层组成以优化基于微泡的医学应用。