Journal
APPLIED PHYSICS LETTERS
Volume 110, Issue 7, Pages -Publisher
AMER INST PHYSICS
DOI: 10.1063/1.4976105
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Funding
- National Institutes of Health [R01-EB018975]
- Human Frontiers Science Program Cross-Disciplinary Postdoctoral Fellowship [LT000637/2016]
- NSF graduate research fellowship [1144469]
- Taipei Veterans General Hospital / National Yang-Ming University Excellent Physician Scientists Cultivation Program [103-Y-A-003]
- Heritage Medical Research Institute
- Burroughs Wellcome Career Award at the Scientific Interface
- Pew Scholarship in the Biomedical Sciences
- Packard Fellowship for Science and Engineering
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Ultrasound imaging is widely used to probe the mechanical structure of tissues and visualize blood flow. However, the ability of ultrasound to observe specific molecular and cellular signals is limited. Recently, a unique class of gas-filled protein nanostructures called gas vesicles (GVs) was introduced as nanoscale (similar to 250 nm) contrast agents for ultrasound, accompanied by the possibilities of genetic engineering, imaging of targets outside the vasculature and monitoring of cellular signals such as gene expression. These possibilities would be aided by methods to discriminate GV-generated ultrasound signals from anatomical background. Here, we show that the nonlinear response of engineered GVs to acoustic pressure enables selective imaging of these nanostructures using a tailored amplitude modulation strategy. Finite element modeling predicted a strongly nonlinear mechanical deformation and acoustic response to ultrasound in engineered GVs. This response was confirmed with ultrasound measurements in the range of 10 to 25MHz. An amplitude modulation pulse sequence based on this nonlinear response allows engineered GVs to be distinguished from linear scatterers and other GV types with a contrast ratio greater than 11.5 dB. We demonstrate the effectiveness of this nonlinear imaging strategy in vitro, in cellulo, and in vivo. Published by AIP Publishing.
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