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dc.contributor.authorFurdella, Kenneth J.
dc.contributor.authorWitte, Russell S.
dc.contributor.authorVande Geest, Jonathan P.
dc.date.accessioned2017-06-23T23:02:11Z
dc.date.available2017-06-23T23:02:11Z
dc.date.issued2017-02-13
dc.identifier.citationTracking delivery of a drug surrogate in the porcine heart using photoacoustic imaging and spectroscopy 2017, 22 (4):041016 Journal of Biomedical Opticsen
dc.identifier.issn1083-3668
dc.identifier.doi10.1117/1.JBO.22.4.041016
dc.identifier.urihttp://hdl.handle.net/10150/624370
dc.description.abstractAlthough 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.sponsorshipNational Science Foundation GK-12 fellowship; Technology Research Initiative Fund (TRIF)en
dc.language.isoenen
dc.publisherSPIE-SOC PHOTO-OPTICAL INSTRUMENTATION ENGINEERSen
dc.relation.urlhttp://biomedicaloptics.spiedigitallibrary.org/article.aspx?doi=10.1117/1.JBO.22.4.041016en
dc.rights© 2017 SPIE.en
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/
dc.subjectphotoacoustic imagingen
dc.subjectcoronary heart diseaseen
dc.subjectleft anterior descending coronary arteryen
dc.subjecttracking diffusionen
dc.subjectdrug-eluting stenten
dc.subjectultrasound imagingen
dc.subjectspectroscopyen
dc.subjectintravascular ultrasounden
dc.titleTracking delivery of a drug surrogate in the porcine heart using photoacoustic imaging and spectroscopyen
dc.typeArticleen
dc.contributor.departmentUniv Arizona, Dept Med Imagingen
dc.identifier.journalJournal of Biomedical Opticsen
dc.description.collectioninformationThis 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.versionFinal published versionen
dc.contributor.institutionUniversity of Pittsburgh, Department of Bioengineering, Pittsburgh, Pennsylvania, United States
dc.contributor.institutionUniversity of Arizona, Department of Medical Imaging, Tucson, Arizona, United States
dc.contributor.institutionUniversity of Pittsburgh, Department of Bioengineering, Pittsburgh, Pennsylvania, United States
refterms.dateFOA2018-09-11T20:25:19Z
html.description.abstractAlthough 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)


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