Abstract

Nanobubbles have gained attention for their use as highly stable ultrasound (US) contrast agents, but assessment of individual nanobubble size remains a challenge. Current sizing techniques require either extensive sample preparation or depend on assumed values of nanobubble density that are not well characterized. An US based approach would be desirable; however, probing individual nanobubbles using US transducers at clinical frequencies is not feasible due to the comparatively long acoustic wavelengths employed. Here we present a technique which can be used to estimate nano- or microbubble size by virtue of the amount of motion detected in an M-Mode image acquired using an acoustic microscope equipped with a 200 MHz transducer. A sample of a bubble-containing solution is incorporated into a phantom composed of molten agarose. The solidified agarose gel contains pores with well-defined sizes dictated by the agarose concentration. Bubbles in the gel matrix that are smaller in diameter than the gel pore size are capable of undergoing stochastic motion which manifests as intensity fluctuations in M-Mode images. Conversely, bubbles which are larger than the agarose pores become trapped and produce static M-Mode intensity patterns. In this study, agarose gels with concentrations ranging from 0.25% to 1.25% (mean pore sizes ranging from 2.68 μm to 0.34 μm) were loaded with either nanobubbles (mean diameter 0.326 μm) or microbubbles (mean diameter 2.71 μm) and imaged at 200 MHz. In the nanobubble loaded gels, M-Mode fluctuations were clearly visible up to a gel concentration of 1% (pore size of 0.39 μm). In contrast, the microbubble loaded gels exhibited minimal M-Mode fluctuation even at agarose concentrations of 0.25% (2.68 μm pore size). Autocorrelation curves generated from the M-Mode data demonstrated a clear trend of curve flattening (loss of motion) when the pore size was comparable to mean bubble diameter, indicating that individual bubbles trapped in the agarose pores are the main source of acoustic backscatter. In the future, decay parameters extracted from the autocorrelation curves could potentially be used as indicators of mean bubble diameter for bubble populations of unknown size.

Highlights

  • The term nanobubble (NB) is used to refer to a bubble with sub-micron diameter, commonly composed of a lipid shell surrounding a gas-core.[1]

  • For the Resonance mass measurement (RMM) system, 2 μL of NB stock was diluted in 1 mL of water

  • The Archimedes system used to measure the NB size automatically selected the limit of detection for each experiment, which determined the cutoff of the lower size limit set for the NB size distribution

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Summary

Introduction

The term nanobubble (NB) is used to refer to a bubble with sub-micron diameter, commonly composed of a lipid shell surrounding a gas-core.[1] NBs have a wide range of industrial applications including cleaning, disinfection, water treatment, and manufacturing of functional materials.[2] In biomedical applications, NBs can be used to deliver therapeutic agents into tumors[3] while providing enhanced ultrasound (US) contrast for diagnostic purposes,[4] and assessing treatment efficacy.[5] When compared to commercial microbubbles (MB), NBs provide similar or better US contrast,[6] have higher mass transportation efficiencies,[2] and have greater temporal stability, with decay half-lives over 10 times longer when used in murine models.[7] As with MBs, the stability and size of a population of NBs is directly related to the composition of their gas core, their shell material, and the presence of membrane stiffeners in their shells.[1] Recently developed ultra-stable NB formulations, such as PGG (Propylene Glycol and Glycerol) NBs,[8] contain perfluorocarbon gas and phospholipids including poly-ethylene glycol (PEG) which further increase in vivo halflife and biocompatibility.[9] Another advantage of NBs is their

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