Key result
Ultrasound-mediated microbubble destruction expands microsphere interstitial dispersion by ~88% versus red blood cells.
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BACKGROUND: We have previously shown that the application of ultrasound to thin-shelled microbubbles flowing through small microvessels (<7 microm in diameter) produces vessel wall ruptures in vivo. Because many intravascular drug- and gene-delivery vehicles are limited by the endothelial barrier, we hypothesized that this phenomenon could be used to deliver drug-bearing vehicles to tissue. METHODS AND RESULTS: An exteriorized rat spinotrapezius muscle preparation was used. Intravascular fluorescent red blood cells and polymer microspheres (PM) (205 and 503 nm in diameter) were delivered to the interstitium of rat skeletal muscle through microvessel ruptures created by insonifying microbubbles in vivo. On intravital microscopy, mean dispersion areas per rupture for red blood cells, 503-nm PM, and 205-nm PM were 14.5x10(3) microm2, 24. 2x10(3) microm2, and 27.2x10(3) microm2, respectively. PM dispersion areas were significantly larger than the mean dispersion area for red blood cells (P<0.05). CONCLUSIONS: Microvessel ruptures caused by insonification of microbubbles in vivo may provide a minimally invasive means for delivering colloidal particles and engineered red blood cells across the endothelial lining of a targeted tissue region.
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Price et al. (1998) studied Microvessel rupture and transendothelial delivery in vivo (rat spinotrapezius muscle preparation). Targeted microbubble destruction with ultrasound delivering polymer microspheres (205-nm and 503-nm) and fluorescent red blood cells vs. Fluorescent red blood cells was evaluated on Mean dispersion area per microvessel rupture in the interstitium (p=<0.05). Ultrasound-mediated microbubble destruction delivered 205-nm and 503-nm microspheres with larger dispersion areas (27.2x10^3 and 24.2x10^3 um2) than red blood cells (14.5x10^3 um2; P<0.05).
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