TY - JOUR
T1 - Secondary Bjerknes Forces Deform Targeted Microbubbles
AU - Kokhuis, Tom J.A.
AU - Garbin, Valeria
AU - Kooiman, Klazina
AU - Naaijkens, Benno A.
AU - Juffermans, Lynda J.M.
AU - Kamp, Otto
AU - van der Steen, Antonius F.W.
AU - Versluis, Michel
AU - de Jong, Nico
PY - 2013
Y1 - 2013
N2 - In this study, we investigated the effect of secondary Bjerknes forces on targeted microbubbles using high-speed optical imaging. We observed that targeted microbubbles attached to an underlying surface and subject to secondary Bjerknes forces deform in the direction of their neighboring bubble, thereby tending toward a prolate shape. The deformation induces an elastic restoring force, causing the bubbles to recoil back to their equilibrium position; typically within 100 μs after low-intensity ultrasound application. The temporal dynamics of the recoil was modeled as a simple mass-spring system, from which a value for the effective spring constant k of the order 10−3 Nm−1 was obtained. Moreover, the translational dynamics of interacting targeted microbubbles was predicted by a hydrodynamic point particle model, including a value of the spring stiffness k of the very same order as derived experimentally from the recoiling curves. For higher acoustic pressures, secondary Bjerknes forces rupture the molecular adhesion of the bubbles to the surface. We used this mutual attraction to quantify the binding force between a single biotinylated microbubble and an avidin-coated surface, which was found to be between 0.9 and 2 nanonewtons (nN). The observation of patches of lipids left at the initial binding site suggests that lipid anchors are pulled out of the microbubble shell, rather than biotin molecules unbinding from avidin. Understanding the effect of ultrasound application on targeted microbubbles is crucial for further advances in the realm of molecular imaging.
AB - In this study, we investigated the effect of secondary Bjerknes forces on targeted microbubbles using high-speed optical imaging. We observed that targeted microbubbles attached to an underlying surface and subject to secondary Bjerknes forces deform in the direction of their neighboring bubble, thereby tending toward a prolate shape. The deformation induces an elastic restoring force, causing the bubbles to recoil back to their equilibrium position; typically within 100 μs after low-intensity ultrasound application. The temporal dynamics of the recoil was modeled as a simple mass-spring system, from which a value for the effective spring constant k of the order 10−3 Nm−1 was obtained. Moreover, the translational dynamics of interacting targeted microbubbles was predicted by a hydrodynamic point particle model, including a value of the spring stiffness k of the very same order as derived experimentally from the recoiling curves. For higher acoustic pressures, secondary Bjerknes forces rupture the molecular adhesion of the bubbles to the surface. We used this mutual attraction to quantify the binding force between a single biotinylated microbubble and an avidin-coated surface, which was found to be between 0.9 and 2 nanonewtons (nN). The observation of patches of lipids left at the initial binding site suggests that lipid anchors are pulled out of the microbubble shell, rather than biotin molecules unbinding from avidin. Understanding the effect of ultrasound application on targeted microbubbles is crucial for further advances in the realm of molecular imaging.
KW - Targeted microbubbles
KW - Binding force
KW - Acoustic radiation force
KW - Secondary Bjerknes force
KW - Translational dynamics
KW - Microbubble detachment
KW - Ultrasound contrast agents
KW - Lipid pullout
KW - Bubble deformation
KW - Molecular imaging
U2 - 10.1016/j.ultrasmedbio.2012.09.025
DO - 10.1016/j.ultrasmedbio.2012.09.025
M3 - Article
SN - 0301-5629
VL - 39
SP - 490
EP - 506
JO - Ultrasound in medicine and biology
JF - Ultrasound in medicine and biology
IS - 3
ER -