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Doxorubicin and paclitaxel loaded microbubbles for ultrasound triggered drug delivery
Journal article   Open access   Peer reviewed

Doxorubicin and paclitaxel loaded microbubbles for ultrasound triggered drug delivery

Michael C Cochran, John Eisenbrey, Richard O Ouma, Michael Soulen and Margaret A Wheatley
International journal of pharmaceutics, v 414(1), pp 161-170
2011
PMID: 21609756
url
https://doi.org/10.1016/j.ijpharm.2011.05.030View
Published, Version of Record (VoR) Open

Abstract

Ultrasound contrast agent Targeted drug delivery Microbubble Nanoparticle Paclitaxel
Ultrasound contrast agents are destroyed with focused ultrasound, resulting in drug loaded polymer fragments less than 400 nm in diameter capable of escaping the leaky vasculature of a tumor and providing a sustained release of drug. A polymer ultrasound contrast agent (UCA) developed in our lab has been shown to greatly reduce in size when exposed to ultrasound, resulting in nanoparticles less than 400 nm in diameter capable of escaping the leaky vasculature of a tumor to provide a sustained release of drug. Previous studies with the hydrophilic drug doxorubicin (DOX) demonstrated enhanced drug delivery to tumors when triggered with ultrasound. However the therapeutic potential has been limited due to the relatively low payload of DOX. This study compares the effects of loading the hydrophobic drug paclitaxel (PTX) on the agent's acoustic properties, drug payload, tumoricidal activity, and the ability to deliver drugs through 400 nm pores. A maximum payload of 129.46 ± 1.80 μg PTX/mg UCA (encapsulation efficiency 71.92 ± 0.99%) was achieved, 20 times greater than the maximum payload of DOX (6.2 μg/mg), while maintaining the acoustic properties. In vitro, the tumoricidal activity of paclitaxel loaded UCA exposed to ultrasound was significantly greater than controls not exposed to ultrasound ( p < 0.0016). This study has shown that PTX loaded UCA triggered with focused ultrasound have the potential to provide a targeted and sustained delivery of drug to tumors.

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Collaboration types
Domestic collaboration
Web of Science research areas
Pharmacology & Pharmacy
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