MR imaging of biodegradable polymeric microparticles: A potential method of monitoring local drug delivery

Gadolinium diethylenetriamine pentaacetic acid (Gd‐DTPA) was encapsulated into biodegradable, bioadhesive polymeric microparticles to enable noninvasive monitoring of their local intravesical delivery with MRI. The microparticles were characterized by contrast agent encapsulation and release kinetic...

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Veröffentlicht in:Magnetic resonance in medicine 2005-03, Vol.53 (3), p.614-620
Hauptverfasser: Chen, Hunter H., Le Visage, Catherine, Qiu, Bensheng, Du, Xiangying, Ouwerkerk, Ronald, Leong, Kam W., Yang, Xiaoming
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Sprache:eng
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Zusammenfassung:Gadolinium diethylenetriamine pentaacetic acid (Gd‐DTPA) was encapsulated into biodegradable, bioadhesive polymeric microparticles to enable noninvasive monitoring of their local intravesical delivery with MRI. The microparticles were characterized by contrast agent encapsulation and release kinetics, T1 relaxation rates, and contrast enhancement in vivo. The level of Gd‐DTPA loading into microparticles was 14.3 ± 0.6 μg/mg polymer. The measured T1 relaxation rates of the microparticles showed a direct dependence on Gd‐DPTA content. Both 1.5T and 4.7T MR scanners were used to image murine bladders instilled intravesically with Gd‐DTPA‐loaded particles in vivo. MR images showed ring‐shaped regions of enhancement inscribing the bladder wall, which were attributed to the microparticles that were preferentially adherent to the mucosa lining the urothelium. The images of controls exhibited no such enhancement. The normalized signal intensities measured from post‐instillation images were significantly greater (P < 0.05) than those in the pre‐instillation images. Contrast enhancement was observed for at least 5 days after the initial instillation, although the enhancement decreased due to microparticle degradation or mucosa renewal. The localized distribution of biodegradable, bioadhesive microparticles encapsulating Gd‐DTPA was successfully visualized with MRI in vivo, allowing particle‐mediated delivery to be temporally and spatially monitored noninvasively. Magn Reson Med 53:614–620, 2005. © 2005 Wiley‐Liss, Inc.
ISSN:0740-3194
1522-2594
DOI:10.1002/mrm.20395