Tracking delivery of a drug surrogate in the porcine heart using photoacoustic imaging and spectroscopy
dc.contributor.author | Furdella, Kenneth J. | |
dc.contributor.author | Witte, Russell S. | |
dc.contributor.author | Vande Geest, Jonathan P. | |
dc.date.accessioned | 2017-06-23T23:02:11Z | |
dc.date.available | 2017-06-23T23:02:11Z | |
dc.date.issued | 2017-02-13 | |
dc.identifier.citation | Tracking delivery of a drug surrogate in the porcine heart using photoacoustic imaging and spectroscopy 2017, 22 (4):041016 Journal of Biomedical Optics | en |
dc.identifier.issn | 1083-3668 | |
dc.identifier.doi | 10.1117/1.JBO.22.4.041016 | |
dc.identifier.uri | http://hdl.handle.net/10150/624370 | |
dc.description.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) | |
dc.description.sponsorship | National Science Foundation GK-12 fellowship; Technology Research Initiative Fund (TRIF) | en |
dc.language.iso | en | en |
dc.publisher | SPIE-SOC PHOTO-OPTICAL INSTRUMENTATION ENGINEERS | en |
dc.relation.url | http://biomedicaloptics.spiedigitallibrary.org/article.aspx?doi=10.1117/1.JBO.22.4.041016 | en |
dc.rights | © 2017 SPIE. | en |
dc.rights.uri | http://rightsstatements.org/vocab/InC/1.0/ | |
dc.subject | photoacoustic imaging | en |
dc.subject | coronary heart disease | en |
dc.subject | left anterior descending coronary artery | en |
dc.subject | tracking diffusion | en |
dc.subject | drug-eluting stent | en |
dc.subject | ultrasound imaging | en |
dc.subject | spectroscopy | en |
dc.subject | intravascular ultrasound | en |
dc.title | Tracking delivery of a drug surrogate in the porcine heart using photoacoustic imaging and spectroscopy | en |
dc.type | Article | en |
dc.contributor.department | Univ Arizona, Dept Med Imaging | en |
dc.identifier.journal | Journal of Biomedical Optics | en |
dc.description.collectioninformation | 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. | en |
dc.eprint.version | Final published version | en |
dc.contributor.institution | University of Pittsburgh, Department of Bioengineering, Pittsburgh, Pennsylvania, United States | |
dc.contributor.institution | University of Arizona, Department of Medical Imaging, Tucson, Arizona, United States | |
dc.contributor.institution | University of Pittsburgh, Department of Bioengineering, Pittsburgh, Pennsylvania, United States | |
refterms.dateFOA | 2018-09-11T20:25:19Z | |
html.description.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) |