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Improvement of depth resolution on photoacoustic imaging using multiphoton absorption

机译:使用多光子吸收提高光声成像的深度分辨率

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Commercial imaging systems, such as computed tomography and magnetic resonance imaging, are frequently used powerful tools for observing structures deep within the human body. However, they cannot precisely visualized several-tens micrometer-sized structures for lack of spatial resolution. In this presentation, we propose photoacoustic imaging using multiphoton absorption technique to generate ultrasonic waves as a means of improving depth resolution. Since the multiphoton absorption occurs at only the focus point and the employed infrared pulses deeply penetrate living tissues, it enables us to extract characteristic features of structures embedded in the living tissue. When nanosecond pulses from a 1064-nm Nd:YAG laser were focused on Rhodamine B/chloroform solution (absorption peak: 540 nm), the peak intensity of the generated photoacoustic signal was proportional to the square of the input pulse energy. This result shows that the photoacoustic signals can be induced by the two-photon absorption of infrared nanosecond pulse laser and also can be detected by a commercial low-frequency MHz transducer. Furthermore, in order to evaluate the depth resolution of multiphoton-photoacoustic imaging, we investigated the dependence of photoacoustic signal on depth position using a 1-mm-thick phantom in a water bath. We found that the depth resolution of two-photon photoacoustic imaging (1064 nm) is greater than that of one-photon photoacoustic imaging (532 nm). We conclude that evolving multiphoton-photoacoustic imaging technology renders feasible the investigation of biomedical phenomena at the deep layer in living tissue.
机译:商业成像系统,例如计算机断层扫描和磁共振成像,通常是用于观察人体深处结构的强大工具。但是,由于缺乏空间分辨率,它们无法精确地可视化数十微米大小的结构。在此演示文稿中,我们提出了使用多光子吸收技术来产生超声波作为改善深度分辨率的手段的光声成像。由于多光子吸收仅发生在焦点上,并且所使用的红外脉冲会深深地穿透生物组织,这使我们能够提取嵌入生物组织中的结构的特征。当将来自1064 nm的Nd:YAG激光器的纳秒脉冲聚焦在若丹明B /氯仿溶液上(吸收峰:540 nm)时,所产生的光声信号的峰强度与输入脉冲能量的平方成正比。该结果表明,光声信号可以由红外纳秒脉冲激光的双光子吸收引起,并且也可以由商业低频MHz换能器检测到。此外,为了评估多光子-光声成像的深度分辨率,我们使用1毫米厚的幻影在水浴中研究了光声信号对深度位置的依赖性。我们发现,二光子光声成像的深度分辨率(1064 nm)大于一光子光声成像的深度分辨率(532 nm)。我们得出的结论是,不断发展的多光子-光声成像技术使在活组织深层进行生物医学现象的研究变得可行。

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