光声断层成像技术用于腹主动脉下段血液与脂质的成像

Photoacoustic tomography uses single-wavelength laser light absorbed by specific chemical bonds in tissue. This absorption causes molecular vibration and transient heating, triggering thermoelastic expansion that produces ultrasonic waves. An ultrasound transducer detects these acoustic waves, yielding composition-specific tomographic images without contrast agents.

Photoacoustic tomography uses 1,100-nanometer light to target blood and 1,210-nanometer light to target lipids. This wavelength selectivity allows users to distinguish between different biological components in the same tissue region. The bond-selective absorption of light at these specific wavelengths enables compositional imaging.

Photoacoustic tomography is rapid, non-invasive, and contrast agent-free, addressing limitations of existing modalities like long acquisition times, high costs, and harmful contrast agents. When combined with ultrasound, it provides structural and compositional information simultaneously. It also enables deeper tissue imaging than other optical techniques without invasive procedures.

Animals are anesthetized with isoflurane and placed on a heated stage with monitoring electrodes and rectal temperature probe. Hair is removed from the abdomen using depilatory cream. The ultrasound transducer is positioned on the abdomen to locate the infrarenal aorta using anatomical landmarks like the left renal vein and aortic trifurcation.

Photoacoustic tomography enables neurobiological applications by detecting deep brain features and hemoglobin oxygenation for evaluating normal and pathological tissue. In vascular medicine, it characterizes plaques as vulnerable or stable, predicting rupture-prone lesions that might cause myocardial infarction or ischemic stroke, supporting near-infrared fluorescence imaging of abdominal aortic aneurysms.

The photoacoustic effect occurs when absorbed light causes molecular vibration and transient heating, producing thermoelastic tissue expansion and ultrasonic wave propagation. Mathematically, the light-induced acoustic wave is governed by the Gruneisen parameter, absorption coefficient, and optical fluence. For each millikelvin temperature rise, an 800-pascal pressure wave is generated and detected.

Photoacoustic tomography uses wavelength-specific imaging: 1,100-nanometer light targets blood within the aorta, while 1,210-nanometer light targets subcutaneous and periaortic fat accumulation. Ultrasound imaging provides structural information to interpret compositional data. Subcutaneous fat follows skin geometry, while periaortic fat follows the aorta's contour.