Amplitude-Modulated Singular Value Decomposition for Ultrafast Ultrasound Imaging of Gas Vesicles
Creators
Abstract
Ultrasound imaging holds significant promise for the observation of molecular and cellular phenomena through the utilization of acoustic contrast agents and acoustic reporter genes. Optimizing imaging methodologies for enhanced detection represents an imperative advancement in this field. Most advanced techniques relying on amplitude modulation schemes such as cross amplitude modulation (xAM) and ultrafast amplitude modulation (uAM) combined with Hadamard encoded multiplane wave transmissions have shown efficacy in capturing the acoustic signals of gas vesicles (GVs). Nonetheless, uAM sequence requires odd- or even-element transmissions leading to imprecise amplitude modulation emitting scheme, and the complex multiplane wave transmission scheme inherently yields overlong pulse durations. xAM sequence is limited in terms of field of view and imaging depth. To overcome these limitations, we introduce an innovative ultrafast imaging sequence called amplitude-modulated singular value decomposition (SVD) processing. Our method demonstrates a contrast imaging sensitivity comparable to the current gold-standard xAM and uAM, while requiring 4.8 times fewer pulse transmissions. With a similar number of transmit pulses, amplitude-modulated SVD outperforms xAM and uAM in terms of an improvement in signal-to-background ratio of +4.78 ±0.35 dB and +8.29 ±3.52 dB, respectively. Furthermore, the method exhibits superior robustness across a wide range of acoustic pressures and enables high-contrast imaging in ex vivo and in vivo settings. Furthermore, amplitude-modulated SVD is envisioned to be applicable for the detection of slow moving microbubbles in ultrasound localization microscopy (ULM).
Copyright and License
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and similar technologies.
Acknowledgement
Mikhail G. Shapiro is an investigator of the Howard Hughes Medical Institute.
Funding
This work was supported in part by the Inserm Research Accelerator (Inserm ART) in Biomedical Ultrasound, in part by the French National Research Agency (ANR) through the Project SonoGT under Grant ANR-21-CE19-0050,
and in part by the Region Ile de France–Convention DIM Empowering Life sciences with Innovative Technologies (ELICIT) Innovative Technologies for Life Science.
Additional details
Funding
- Inserm research accelerator
- Inserm research accelerator (Inserm ART) in Biomed
- French national research agency
- ANR-21-CE19-0050 program (Project SonoGT)
- Region Ile de France - Convention DIM ELICIT Innovative Technologies for Life Science
Dates
- Submitted
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2025-04-02
- Accepted
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2025-04-24
- Available
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2025-04-28Published
- Available
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2025-08-01Version of record
Caltech Custom Metadata
- Caltech groups
- Division of Chemistry and Chemical Engineering (CCE) , Division of Engineering and Applied Science (EAS)
- Publication Status
- Published