In Vivo Near-Infrared Fluorescence Imaging of Atherosclerosis Using Local Delivery of Novel Targeted Molecular Probes.
Animals
Aorta
/ metabolism
Atherosclerosis
/ diagnosis
Collagen Type I
/ metabolism
Feasibility Studies
Fluorescent Dyes
/ chemistry
Humans
Intercellular Adhesion Molecule-1
/ metabolism
Male
Molecular Probes
/ chemistry
Optical Imaging
/ methods
Plaque, Atherosclerotic
/ diagnosis
Rabbits
Reproducibility of Results
Spectroscopy, Near-Infrared
/ methods
Ultrasonography, Interventional
/ methods
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
25 02 2019
25 02 2019
Historique:
received:
03
05
2018
accepted:
08
01
2019
entrez:
27
2
2019
pubmed:
26
2
2019
medline:
15
9
2020
Statut:
epublish
Résumé
This study aimed to evaluate the feasibility and accuracy of a technique for atherosclerosis imaging using local delivery of relatively small quantities (0.04-0.4 mg/kg) of labeled-specific imaging tracers targeting ICAM-1 and unpolymerized type I collagen or negative controls in 13 rabbits with atheroma induced by balloon injury in the abdominal aorta and a 12-week high-cholesterol diet. Immediately after local infusion, in vivo intravascular ultrasonography (IVUS)-NIRF imaging was performed at different time-points over a 40-minute period. The in vivo peak NIRF signal was significantly higher in the molecular tracer-injected rabbits than in the control-injected animals (P < 0.05). Ex vivo peak NIRF signal was significantly higher in the ICAM-1 probe-injected rabbits than in controls (P = 0.04), but not in the collagen probe-injected group (P = 0.29). NIRF signal discrimination following dual-probe delivery was also shown to be feasible in a single animal and thus offers the possibility of combining several distinct biological imaging agents in future studies. This innovative imaging strategy using in vivo local delivery of low concentrations of labeled molecular tracers followed by IVUS-NIRF catheter-based imaging holds potential for detection of vulnerable human coronary artery plaques.
Identifiants
pubmed: 30804367
doi: 10.1038/s41598-019-38970-4
pii: 10.1038/s41598-019-38970-4
pmc: PMC6389905
doi:
Substances chimiques
Collagen Type I
0
Fluorescent Dyes
0
Molecular Probes
0
Intercellular Adhesion Molecule-1
126547-89-5
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2670Subventions
Organisme : CIHR
ID : 273578
Pays : Canada
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