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首页> 外文期刊>Photodiagnosis and Photodynamic Therapy >Photoacoustic diagnosis of pharmacokinetics and vascular shutdown effects in photodynamic treatment with indocyanine green-lactosome for a subcutaneous tumor in mice
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Photoacoustic diagnosis of pharmacokinetics and vascular shutdown effects in photodynamic treatment with indocyanine green-lactosome for a subcutaneous tumor in mice

机译:对小鼠皮下肿瘤的吲哚菁绿乳酸光动力学治疗的药代动力学和血管关断效应的光声诊断

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摘要

Indocyanine green lactosome (ICG-lactosome) is an attractive new-generation agent for photodynamic therapy (PDT) that is characterized by a near-infrared excitation wavelength and high stability in the bloodstream. Fluorescence imaging has been used to examine its pharmacokinetics in vivo, but no depth-resolved information can be obtained with this method. In this study, we applied photoacoustic (PA) imaging to visualize the depth distribution of ICG-lactosome in a mouse subcutaneous tumor model. With this method, the depth distribution of blood vessels can also be visualized, enabling detection of vascular shutdown effects due to PDT. We performed PA imaging of both the distributions of ICG-lactosome and blood vessels in a tumor before and after PDT, and we found that PA signals originating from ICG-lactosome were greatly increased at 18 h after drug injection but rapidly decreased after PDT. These results indicate efficient accumulation of ICG-lactosome and rapid photo bleaching due to the PDT reaction in the tumor, respectively. After PDT, PA amplitudes of hemoglobin were significantly decreased, being attributable to vascular shutdown effects. These results show the usefulness of PA imaging for monitoring not only photosensitizer accumulation and bleaching but also vascular responses in PDT with ICG-lactosome. This method can be applied to the diagnosis of many types of PDT processes.
机译:吲哚菁绿色乳酸(ICG-乳酸杆菌)是一种用于光动力治疗(PDT)的有吸引力的新一代剂,其特征在于近红外激发波长和血液中的高稳定性。荧光成像已用于在体内检查其药代动力学,但没有通过该方法获得深度分辨的信息。在这项研究中,我们施加了光声(PA)成像,以使小鼠皮下肿瘤模型中ICG-乳糜体的深度分布。通过这种方法,还可以可视化血管的深度分布,从而能够检测由于PDT引起的血管停机效应。我们在PDT之前和之后进行了肿瘤中ICG-嗜睡和血管分布的PA成像,我们发现,在注射药物注射后18小时,源自ICG-乳糜体的PA信号大大增加,但在PDT后迅速降低。这些结果分别表示由于肿瘤中的PDT反应而有效地积累ICG-乳酸和快速光照漂白。 PDT后,血红蛋白的PA振荡显着降低,可归因于血管停机效应。这些结果表明,PA成像用于监测的有用性,不仅是光敏剂积聚和漂白,而且在PDT与ICG-乳糜组体中的血管反应。该方法可以应用于许多类型的PDT过程的诊断。

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