Skip to main content
. Author manuscript; available in PMC: 2018 Apr 1.
Published in final edited form as: Mol Imaging Biol. 2017 Apr;19(2):194–202. doi: 10.1007/s11307-016-0991-4

Fig. 1.

Fig. 1

Data acquisition and image processing flow for both superharmonic (acoustic angiography; top row) and multi-pulse (bottom row) ultrasound molecular imaging. All animals were imaged using both systems on the same day. a 3D B-mode and contrast-specific pre-scans are acquired using a motorized motion stage. b Targeted contrast agent is administered and 3D images are acquired in contrast-specific imaging modes after a 12 min wait. Targeted bubbles are then destroyed by high MI scanning, and a post-scan is acquired. c Free microbubbles are administered and a microvascular imaging or “acoustic angiography” scan is acquired for the superharmonic imaging case only. Using the described data sets, it is now possible to combine d 3D molecular imaging data sets on both systems, with e either vascular or B-mode data to produce f combined visualizations of anatomical and functional imaging data.