TY - JOUR
T1 - A Dual-Modality Hybrid Imaging System Harnesses Radioluminescence and Sound to Reveal Molecular Pathology of Atherosclerotic Plaques
AU - Zaman, Raiyan T.
AU - Yousefi, Siavash
AU - Long, Steven R.
AU - Saito, Toshinobu
AU - Mandella, Michael
AU - Qiu, Zhen
AU - Chen, Ruimin
AU - Contag, Christopher H.
AU - Gambhir, Sanjiv S.
AU - Chin, Frederick T.
AU - Khuri-Yakub, Butras T.
AU - McConnell, Michael V.
AU - Shung, K. Kirk
AU - Xing, Lei
N1 - Funding Information:
The authors of this manuscript are gratefully acknowledge the help of Mr. Eric Marple, Kirk Urmey from Emvision LLC for machining the stainless steel tubes for the probe packaging; Mr. Matthew Chuck from the Stanford University Physics Machine Shop for machining the scintillating imaging window; Dr. Paul Cristman for helping us with the trouble shooting of our PAT system; Drs. Ronald L. Dalman, Matthew Mell, Jason T. Lee, Venita Chandra for providing human endarterectomy samples. The authors of this study are gratefully acknowledge the following funding agencies for supporting their research work. This study was fully supported by the NIH K99/R00 award (1 K99 HL127180-01), partly supported by generous gifts from the Chambers Family Foundation for Excellence in Pediatric Research (CHC), the Child Health Research Institute (CHRI) at Stanford (CHC), and an NIH Shared Instrumentation Grant (S10OD010344-01A1).
Funding Information:
This study was fully supported by the NIH K99/R00 award (1 K99 HL127180-01), partly supported by generous gifts from the Chambers Family Foundation for Excellence in Pediatric Research (CHC), the Child Health Research Institute (CHRI) at Stanford (CHC), and an NIH Shared Instrumentation Grant (S10OD010344-01A1)
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Atherosclerosis is a progressive inflammatory condition caused by an unstable lesion, called thin-cap fibro atheromata (TCFA) that underlies coronary artery disease (CAD) - one of the leading causes of death worldwide. Therefore, early clinical diagnosis and effective risk stratification is important for CAD management as well as preventing progression to catastrophic events. However, early detection could be difficult due to their small size, motion, obscuring 18F-FDG uptake by adjacent myocardium, and complex morphological/biological features. To overcome these limitations, we developed a catheter-based Circumferential-Intravascular-Radioluminescence-Photoacoustic-Imaging (CIRPI) system that can detect vulnerable plaques in coronary arteries and characterizes them with respect to pathology and biology. Our CIRPI system combined two imaging modalities: Circumferential Radioluminescence Imaging (CRI) and PhotoAcoustic Tomography (PAT) within a novel optical probe. The probe's CaF2:Eu based scintillating imaging window provides a 360° view of human (n = 7) and murine carotid (n = 10) arterial plaques by converting β-particles into visible photons during 18F-FDG decay. A 60× and 63× higher radioluminescent signals were detected from the human and murine plaque inflammations, respectively, compared to the control. The system's photoacoustic imaging provided a comprehensive analysis of the plaque compositions and its morphologic information. These results were further verified with IVIS-200, immunohistochemical analysis, and autoradiography.
AB - Atherosclerosis is a progressive inflammatory condition caused by an unstable lesion, called thin-cap fibro atheromata (TCFA) that underlies coronary artery disease (CAD) - one of the leading causes of death worldwide. Therefore, early clinical diagnosis and effective risk stratification is important for CAD management as well as preventing progression to catastrophic events. However, early detection could be difficult due to their small size, motion, obscuring 18F-FDG uptake by adjacent myocardium, and complex morphological/biological features. To overcome these limitations, we developed a catheter-based Circumferential-Intravascular-Radioluminescence-Photoacoustic-Imaging (CIRPI) system that can detect vulnerable plaques in coronary arteries and characterizes them with respect to pathology and biology. Our CIRPI system combined two imaging modalities: Circumferential Radioluminescence Imaging (CRI) and PhotoAcoustic Tomography (PAT) within a novel optical probe. The probe's CaF2:Eu based scintillating imaging window provides a 360° view of human (n = 7) and murine carotid (n = 10) arterial plaques by converting β-particles into visible photons during 18F-FDG decay. A 60× and 63× higher radioluminescent signals were detected from the human and murine plaque inflammations, respectively, compared to the control. The system's photoacoustic imaging provided a comprehensive analysis of the plaque compositions and its morphologic information. These results were further verified with IVIS-200, immunohistochemical analysis, and autoradiography.
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U2 - 10.1038/s41598-018-26696-8
DO - 10.1038/s41598-018-26696-8
M3 - Article
C2 - 29895966
AN - SCOPUS:85048793159
SN - 2045-2322
VL - 8
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 8992
ER -