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Monitoring of the tumor response to nano-graphene oxide-mediated photothermal/photodynamic therapy by diffusion-weighted and BOLD MRI

机译:监测肿瘤反应nano-grapheneoxide-mediated光热光谱分析/光动力治疗diffusion-weighted和大胆的核磁共振

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摘要

Photothermal therapy (PTT) and photodynamic therapy (PDT) are promising cancer treatment modalities. Because each modality has its own set of advantages and limitations, there has been interest in developing methods that can co-deliver the two regimens for enhanced tumor treatment. Among the efforts, nano-graphene oxide-mediated phototherapies have recently attracted much attention. Nano-graphene oxide has a broad absorbance spectrum and can be loaded with photosensitizers, such as chlorin e6, with high efficiency. Chlorin e6-loaded and PEGylated nano-graphene (GO-PEG-Ce6) can be excited at 660 nm, 808 nm, or both, to induce PDT, PTT, or PDT/PTT combination. Despite the potential of the treatments, there is a lack of a diagnostic tool which can monitor their therapeutic response in a noninvasive and prognostic manner; such an ability is urgently needed for the transformation and translation of the technologies. In this study, we performed diffusion-weighted and blood oxygenation level dependent (BOLD) magnetic resonance imaging (MRI) after GO-PEG-Ce6-mediated PTT, PDT, or PTT/PDT. We found that after efficient PTT, there is a significant increase of the tumor apparent diffusion coefficient (ADC) value in diffusion-weighted imaging (DWI) maps; meanwhile, an efficient PDT led to an increase of R-2* in BOLD images. In both the cases, the amplitude of the ADC/R-2* increase was correlated with the treatment outcomes. More interestingly, a synergistic treatment efficacy was observed when the PTT/PDT combination was applied, and the combination was associated with a greater ADC and R-2* increase than when either modality was used alone. In particular, the PTT/PDT condition that induced the most dramatic short-term increase of the ADC value (>70%) caused the most effective tumor control in the long-run, with 60% of the treated animals being tumor-free after 60 days. These results suggest the great promise of the combination of DWI and BOLD MRI as a tool for accurate monitoring and prognosis of phototherapies, which is of great value to the future developments of the methodologies.
机译:光照疗法(PTT)和光能疗法(PDT)是有前途的癌症治疗形式。的优势和局限性,兴趣发展的方法co-deliver增强肿瘤的两种方案治疗。oxide-mediated光疗最近吸引了很多注意力。广泛的吸收光谱,可以加载敏化,如氯e6效率高。在660 nano-graphene (GO-PEG-Ce6)可以兴奋nm, 808海里,或者两者兼有,诱导PDT, PTT、PDT / PTT的组合。治疗,缺乏一种诊断工具可以监视他们的治疗反应非侵入性和预后的方式;能力是迫切需要的转变和翻译的技术。研究中,我们表现diffusion-weighted和血液氧化程度依赖(粗体)磁磁共振成像(MRI) GO-PEG-Ce6-mediated之后PTT、PDT或PTT / PDT。有效的PTT,有显著增加肿瘤表观扩散系数(ADC)价值diffusion-weighted成像(驾车)地图;与此同时,一个高效的PDT导致增加r2 *粗体图像。ADC的振幅/ r2 *增加相关治疗结果。协同治疗疗效观察PTT / PDT组合应用时,被关联到一个更大的ADC和组合r2 *增加比形态时使用一个人。诱导最引人注目的短期增长ADC值(> 70%)最有效的引起的在长期肿瘤控制,60%的对待动物是患肿瘤后60天。这些结果说明伟大的承诺醉酒驾车和大胆的磁共振成像作为一种工具准确的监测和预后光疗,具有十分重要的价值未来发展的方法。

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