Tracking delivery of a drug surrogate in the porcine heart using photoacoustic imaging and spectroscopy

被引:5
|
作者
Furdella, Kenneth J. [1 ]
Witte, Russell S. [2 ]
Vande Geest, Jonathan P. [1 ]
机构
[1] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA 15260 USA
[2] Univ Arizona, Dept Med Imaging, Tucson, AZ USA
基金
美国国家科学基金会;
关键词
photoacoustic imaging; coronary heart disease; left anterior descending coronary artery; tracking diffusion; drug-eluting stent; ultrasound imaging; spectroscopy; intravascular ultrasound; PACLITAXEL-ELUTING STENTS; CORONARY ANGIOPLASTY; TRANSPORT-PROPERTIES; LOCATION; RESTENOSIS; RAPAMYCIN;
D O I
10.1117/1.JBO.22.4.041016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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)
引用
收藏
页数:7
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