Tracking delivery of a drug surrogate in the porcine heart using photoacoustic imaging and spectroscopy
Affiliation
Univ Arizona, Dept Med ImagingIssue Date
2017-02-13Keywords
photoacoustic imagingcoronary heart disease
left anterior descending coronary artery
tracking diffusion
drug-eluting stent
ultrasound imaging
spectroscopy
intravascular ultrasound
Metadata
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Tracking delivery of a drug surrogate in the porcine heart using photoacoustic imaging and spectroscopy 2017, 22 (4):041016 Journal of Biomedical OpticsJournal
Journal of Biomedical OpticsRights
© 2017 SPIE.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Although the drug-eluting stent (DES) has dramatically reduced the rate of coronary restenosis, it still occurs in up to 20% of patients with a DES. Monitoring drug delivery could be one way to decrease restenosis rates. We demonstrate real-time photoacoustic imaging and spectroscopy (PAIS) using a wavelength-tunable visible laser and clinical ultrasound scanner to track cardiac drug delivery. The photoacoustic signal was initially calibrated using porcine myocardial samples soaked with a known concentration of a drug surrogate (Dil). Next, an in situ coronary artery was perfused with DiI for 20 min and imaged to monitor dye transport in the tissue. Finally, a partially DiI-coated stent was inserted into the porcine brachiocephalic trunk for imaging. The photoacoustic signal was proportional to the DiI concentration between 2.4 and 120 mu g/ml, and the dye was detected over 1.5 mm from the targeted coronary vessel. Photoacoustic imaging was also able to differentiate the DiI-coated portion of the stent from the uncoated region. These results suggest that PAIS can track drug delivery to cardiac tissue and detect drugs loaded onto a stent with sub-mm precision. Future work using PAIS may help improve DES design and reduce the probability of restenosis. (C) 2017 Society of Photo-Optical Instrumentation Engineers (SPIE)ISSN
1083-3668Version
Final published versionSponsors
National Science Foundation GK-12 fellowship; Technology Research Initiative Fund (TRIF)Additional Links
http://biomedicaloptics.spiedigitallibrary.org/article.aspx?doi=10.1117/1.JBO.22.4.041016ae974a485f413a2113503eed53cd6c53
10.1117/1.JBO.22.4.041016