This work was motivated by an ongoing development of a potential embolotherapy technique to occlude blood flow to tumors using gas bubbles selectively formed by in vivo acoustic droplet vaporization (ADV) of liquid perfluorocarbon droplets. Mechanisms behind the ADV, transport and lodging of emboli need to be understood before gas embolotherapy can translate to the clinic.

Evolution of a bubble from acoustic droplet vaporization in a rigid tube, under physiological and room temperature conditions, was observed via ultra-high speed imaging. Effective radii and radial expansion ratios were obtained by processing the images using Image] software. At physiological temperature, a radial expansion ratio of 5.05 was attained, consistent with theoretical prediction. The initial radial growth rate was linear, after which the growth rate increased proportionally with square root of time. Nondimensionalization revealed that the subsequent growth rate also varied inversely with square root of initial radius. Eventually growth became asymptotic. No collapse was observed.

A theoretical model derived from a modified Bernoulli equation, and a computational model by Ye & Bull (2004), were compared respectively with experimental results. Initial growth rates were predicted correctly by both models. Experimental results showed heavy damping of growth rate as the bubble grew towards the wall, whereas both models predicted an overshoot in growth followed by multiple oscillations. The theoretical model broke down near the wall; the computational model gave a reasonable bubble shape near the wall but would require correct initial pressure values to be accurate.

At room temperature, the expansion ratio shot to 1.43 initially and oscillated down to 1.11, far below the theoretical prediction. Failure of the bubble to expand fully could be due to unconsumed or condensed liquid perfluorocarbon.

A new fabrication method via non-lithographic means was devised to make a circular-lumen microchannel out of PDMS, with a diameter as small as 80 microns to mimic the size of a medium arteriole. The microchannel was endothelialized successfully, with a fairly homogeneous distribution along the length. Cell viability assays confirmed the viability of cells maintained in the microchannel. Bubble motion experiments performed with the benchtop microvascular model demonstrated its feasibility.