4.5 Article

VISUALIZING THE HISTOTRIPSY PROCESS: BUBBLE CLOUD-CANCER CELL INTERACTIONS IN A TISSUE-MIMICKING ENVIRONMENT

期刊

ULTRASOUND IN MEDICINE AND BIOLOGY
卷 42, 期 10, 页码 2466-2477

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ultrasmedbio.2016.05.018

关键词

Histotripsy; Cavitation; Cancer; Cell-bubble interactions; Tissue fractionation

资金

  1. National Science Foundation Graduate Research Fellowship
  2. National Institute of Biomedical Imaging and Bioengineering (NIBIB) of the National Institutes of Health (NIH) [R01 EB008998]
  3. National Institute of Neurological Disorders and Stroke (NINDS) of the NIH [R21 NS093121]
  4. American Cancer Society [RSG-13-101-01-CCE]
  5. National Science Foundation [CBET 1253157]
  6. Hartwell Foundation
  7. Directorate For Engineering
  8. Div Of Chem, Bioeng, Env, & Transp Sys [1253157] Funding Source: National Science Foundation

向作者/读者索取更多资源

Histotripsy is a non-invasive ultrasonic ablation method that uses cavitation to mechanically fractionate tissue into acellular debris. With a sufficient number of pulses, histotripsy can completely fractionate tissue into a liquid-appearing homogenate with no cellular structures. The location, shape and size of lesion formation closely match those of the cavitation cloud. Previous work has led to the hypothesis that the rapid expansion and collapse of histotripsy bubbles fractionate tissue by inducing large stress and strain on the tissue structures immediately adjacent to the bubbles. In the work described here, the histotripsy bulk tissue fractionation process is visualized at the cellular level for the first time using a custom-built 2-MHz transducer incorporated into a microscope stage. A layer of breast cancer cells were cultured within an optically transparent fibrin-based gel phantom to mimic cells inside a 3-D extracellular matrix. To test the hypothesis, the cellular response to single and multiple histotripsy pulses was investigated using high-speed optical imaging. Bubbles were always generated in the extracellular space, and significant cell displacement/deformation was observed for cells directly adjacent to the bubble during both bubble expansion and collapse. The largest displacements were observed during collapse for cells immediately adjacent to the bubble, with cells moving more than 150-300 mu m in less than 100 mu s. Cells often underwent multiple large deformations (>150% strain) over multiple pulses, resulting in the bisection of cells multiple times before complete removal. To provide theoretical support to the experimental observations, a numerical simulation was conducted using a single-bubble model, which indicated that histotripsy exerts the largest strains and cell displacements in the regions immediately adjacent to the bubble. The experimental and simulation results support our hypothesis, which helps to explain the formation of the sharp lesions formed in histotripsy therapy localized to the regions directly exposed to the bubbles. (C) 2016 World Federation for Ultrasound in Medicine & Biology.

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