...
首页> 外文期刊>Theranostics >WST11 Vascular Targeted Photodynamic Therapy Effect Monitoring by Multispectral Optoacoustic Tomography (MSOT) in Mice
【24h】

WST11 Vascular Targeted Photodynamic Therapy Effect Monitoring by Multispectral Optoacoustic Tomography (MSOT) in Mice

机译:WST11通过多光谱光声层析成像(MSOT)监测小鼠的血管靶向光动力治疗效果。

获取原文

摘要

Objective: Monitoring emerging vascular-targeted photodynamic therapy (VTP) and understanding the time-dynamics of treatment effects remains challenging. We interrogated whether handheld multispectral optoacoustic tomography (MSOT) could noninvasively monitor the effect of VTP using WST11, a vascular-acting photosensitizer, on tumor tissues over time using a renal cell cancer mouse model. We also investigated whether MSOT illumination can induce VTP, to implement a single-modality theranostic approach. Materials and Methods: Eight BalB/c mice were subcutaneously implanted with murine renal adenocarcinoma cells (RENCA) on the flank. Three weeks later VTP was performed (10 min continuous illumination at 753 nm following intravenous infusion) using WST11 or saline as control. Handheld MSOT images were collected prior to VTP administration and subsequently thereafter over the course of the first hour, at 24 and 48 h. Data collected were unmixed for blood oxygen saturation in tissue (SO2) based on the spectral signatures of deoxy- and oxygenated hemoglobin. Changes in oxygen saturation over time, relative to baseline, were examined by paired t-test for statistical significance (p 2 decreased by more than 60% over baseline (p 0.1) in the sham-treated group. Moreover, unlike in the control group, SO2 in treated tumors further decreased over the course of 24 to 48 h post-treatment, concomitant with the propagation of profound central tumor necrosis present in histological analysis. We further show that pulsed MSOT illumination can activate WST11 as efficiently as the continuous wave irradiation employed for treatment. Conclusion: Handheld MSOT non-invasively monitored WST11-VTP effects based on the SO2 signal and detected blood saturation changes within the first 20 min post-treatment. MSOT may potentially serve as a means for both VTP induction and real-time VTP monitoring in a theranostic approach.
机译:目的:监测新兴的以血管为靶标的光动力疗法(VTP)并了解治疗效果的时间动态性仍然具有挑战性。我们询问了手持多光谱光声层析成像(MSOT)是否可以使用肾细胞癌小鼠模型随时间推移使用WST11(一种血管作用光敏剂)对肿瘤组织进行无创监测VTP的效果。我们还调查了MSOT照明是否可以诱导VTP,以实现单模态治疗方法。材料与方法:将八只BalB / c小鼠皮下植入鼠肾腺癌细胞(RENCA)。三周后,使用WST11或生理盐水作为对照,进行VTP(静脉输注后在753 nm处连续照明10分钟)。在VTP给药之前和随后的第一个小时的24小时和48小时内,收集了手持MSOT图像。根据脱氧和氧合血红蛋白的光谱特征,将收集的数据进行混合以获取组织中的血氧饱和度(SO 2 )。通过配对t-检验检验了相对于基线的氧饱和度随时间的变化的统计学显着性(在假治疗组中,p 2 比基线(p 0.1)降低了60%以上。在对照组中,治疗后肿瘤中的SO 2 在治疗后24至48小时内进一步降低,与组织学分析中所见的深部中央肿瘤坏死的扩散相伴。结论:基于SO 2 信号的手持式MSOT无创监测WST11-VTP效应并检测到前20个血中饱和度变化,MSOT照明可以像连续波照射一样有效地激活WST11。 MSOT可能可以作为治疗诊断方法中的VTP诱导和实时VTP监测的手段。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号