On-chip preparation of nanoscale contrast agents towards high-resolution ultrasound imaging

Micron-sized lipid-stabilised bubbles of heavy gas have been utilised as contrast agents for diagnostic ultrasound (US) imaging for many years. Typically bubbles between 1 and 8 μm in diameter are produced to enhance imaging in US by scattering sound waves more efficiently than surrounding tissue. A...

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Published inLab on a chip Vol. 16; no. 4; pp. 679 - 687
Main Authors Peyman, Sally A, McLaughlan, James R, Abou-Saleh, Radwa H, Marston, Gemma, Johnson, Benjamin R. G, Freear, Steven, Coletta, P. Louise, Markham, Alexander F, Evans, Stephen D
Format Journal Article
LanguageEnglish
Published England 01.01.2016
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Summary:Micron-sized lipid-stabilised bubbles of heavy gas have been utilised as contrast agents for diagnostic ultrasound (US) imaging for many years. Typically bubbles between 1 and 8 μm in diameter are produced to enhance imaging in US by scattering sound waves more efficiently than surrounding tissue. A potential area of interest for Contrast Enhanced Ultrasound (CEUS) are bubbles with diameters <1 μm or 'nanobubbles.' As bubble diameter decreases, ultrasonic resonant frequency increases, which could lead to an improvement in resolution for high-frequency imaging applications when using nanobubbles. In addition, current US contrast agents are limited by their size to the vasculature in vivo . However, molecular-targeted nanobubbles could penetrate into the extra-vascular space of cancerous tissue providing contrast in regions inaccessible to traditional microbubbles. This paper reports a new microfluidic method for the generation of sub-micron sized lipid stabilised particles containing perfluorocarbon (PFC). The nanoparticles are produced in a unique atomisation-like flow regime at high production rates, in excess of 10 6 particles per s and at high concentration, typically >10 11 particles per mL. The average particle diameter appears to be around 100-200 nm. These particles, suspected of being a mix of liquid and gaseous C 4 F 10 due to Laplace pressure, then phase convert into nanometer sized bubbles on the application of US. In vitro ultrasound characterisation from these nanoparticle populations showed strong backscattering compared to aqueous filled liposomes of a similar size. The nanoparticles were stable upon injection and gave excellent contrast enhancement when used for in vivo imaging, compared to microbubbles with an equivalent shell composition. We present the first on-chip atomisation-like production of phase-change contrast agents at high concentrations towards high-resolution contrast imaging for diagnostic ultrasound.
Bibliography:vs.
Electronic supplementary information (ESI) available: Supporting information S1: video of a bubble sample in a viewing chamber showing microbubbles rising to the top and underneath a population of smaller bubbles moving with Brownian motion. Supporting information S2: high speed imaging of the microspray regime (100 000 000 fps) showing the velocity of the microspray was still too high to capture single bubble formation. Supporting information S3: effect of lipid concentration on microspray particle size and concentration. S4: expansion ratio model used to calculate the predicted increase in nanoparticle diameter on the increase of temperature in Fig. 4a from
ref. 42
Supporting information S5: comparison of lipid solution only passing through tubes of the set-up compared to lipid solution going through the microfluidic device. S6: plot to show change in resonant frequency
observations in Fig. 7, TIC curves for microbubble only and nanobubble only. See DOI
in vivo
10.1039/c5lc01394a
bubble diameter. S7: time
intensity curves to support
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ISSN:1473-0197
1473-0189
DOI:10.1039/c5lc01394a