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- Special Collection: Molecular Imaging
- Lindner, Jonathan RRemove Lindner, Jonathan R filter
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Special Collection: Molecular Imaging
2 Results
- Review
Seeing the Invisible—Ultrasound Molecular Imaging
Ultrasound in Medicine and BiologyVol. 46Issue 3p479–497Published online: December 30, 2019- Alexandra Kosareva
- Lotfi Abou-Elkacem
- Sayan Chowdhury
- Jonathan R. Lindner
- Beat A. Kaufmann
Cited in Scopus: 28Ultrasound molecular imaging has been developed in the past two decades with the goal of non-invasively imaging disease phenotypes on a cellular level not depicted on anatomic imaging. Such techniques already play a role in pre-clinical research for the assessment of disease mechanisms and drug effects, and are thought to in the future contribute to earlier diagnosis of disease, assessment of therapeutic effects and patient-tailored therapy in the clinical field. In this review, we first describe the chemical composition and structure as well as the in vivo behavior of the ultrasound contrast agents that have been developed for molecular imaging. - Original Contribution
Ultrasound Molecular Imaging of Atherosclerosis Using Small-Peptide Targeting Ligands Against Endothelial Markers of Inflammation and Oxidative Stress
Ultrasound in Medicine and BiologyVol. 44Issue 6p1155–1163Published online: March 13, 2018- Federico Moccetti
- Craig C. Weinkauf
- Brian P. Davidson
- J. Todd Belcik
- Edmund R. Marinelli
- Evan Unger
- and others
Cited in Scopus: 23The aim of this study was to evaluate a panel of endothelium-targeted microbubble (MB) ultrasound contrast agents bearing small peptide ligands as a human-ready approach for molecular imaging of markers of high-risk atherosclerotic plaque. Small peptide ligands with established affinity for human P-selectin, VCAM-1, LOX-1 and von Willebrand factor (VWF) were conjugated to the surface of lipid-stabilized MBs. Contrast-enhanced ultrasound (CEUS) molecular imaging of the thoracic aorta was performed in wild-type and gene-targeted mice with advanced atherosclerosis (DKO).