Ryerson University, Department of Physics, Toronto, Canada.
Institute for Biomedical Engineering, Science and Technology, St. Michael's Hospital, Keenan Researc, Canada.
J Biomed Opt. 2019 Nov;24(11):1-8. doi: 10.1117/1.JBO.24.11.116001.
Solid tumors are typically supplied nutrients by a network of irregular blood vessels. By targeting these vascular networks, it might be possible to hinder cancer growth and metastasis. Vascular disrupting agents induce intertumoral hemorrhaging, making photoacoustic (PA) imaging well positioned to detect bleeding due to its sensitivity to hemoglobin and its various states. We introduce a fractal-based numerical model of intertumoral hemorrhaging to simulate the PA signals from disrupted tumor blood vessels. The fractal model uses bifurcated cylinders to represent vascular trees. To mimic bleeding from blood vessels, hemoglobin diffusion from microvessels was simulated. In the simulations, the PA signals were detected by a linear array transducer (30 MHz center frequency) of four different vascular trees. The power spectrum of each beamformed PA signal was computed and fitted to a straight line within the −6-dB bandwidth of the receiving transducer. The spectral slope and midband fit (MBF) based on the fit decreased by 0.11 dB / MHz and 2.12 dB, respectively, 1 h post bleeding, while the y-intercept increased by 1.21 dB. The results suggest that spectral PA analysis can be used to measure changes in the concentration and spatial distribution of hemoglobin in tissue without the need to resolve individual vessels. The simulations support the feasibility of using PA imaging and spectral analysis in cancer treatment monitoring by detecting microvessel disruption.
实体瘤通常由不规则的血管网络供应营养。通过靶向这些血管网络,有可能阻碍癌症的生长和转移。血管破坏剂诱导肿瘤间出血,使得光声(PA)成像非常适合检测由于其对血红蛋白及其各种状态的敏感性而导致的出血。我们引入了一种基于分形的肿瘤间出血数值模型,以模拟从受损肿瘤血管发出的 PA 信号。分形模型使用分叉圆柱来表示血管树。为了模拟血管出血,模拟了从微血管扩散的血红蛋白。在模拟中,线性阵列换能器(30 MHz 中心频率)检测了四个不同血管树的 PA 信号。计算了每个波束形成的 PA 信号的功率谱,并在接收换能器的−6 dB 带宽内拟合为一条直线。拟合后的光谱斜率和中带拟合(MBF)分别降低了 0.11 dB / MHz 和 2.12 dB,而 y 截距增加了 1.21 dB。结果表明,光谱 PA 分析可用于测量组织中血红蛋白浓度和空间分布的变化,而无需分辨单个血管。这些模拟支持了使用 PA 成像和光谱分析在癌症治疗监测中检测微血管破坏的可行性。