Walter Alec B, Jansen E Duco
Vanderbilt University, Department of Biomedical Engineering, Nashville, Tennessee, United States.
Vanderbilt University, Biophotonics Center, Nashville, Tennessee, United States.
J Biomed Opt. 2025 Dec;30(Suppl 3):S34103. doi: 10.1117/1.JBO.30.S3.S34103. Epub 2025 May 28.
Current methods of measuring dosimetry for photodynamic therapy (PDT) have proven to be inadequate in their inability to provide accurate, real-time, and spatially resolved monitoring without interrupting the PDT treatment.
Our goal was to develop and validate a combined treatment and dosimetry system capable of monitoring implicit and explicit dosimetry in real time during non-contact PDT.
By employing both fluorescence imaging and spatial frequency domain imaging (SFDI), designed with low-cost, off-the-shelf components, the combined imaging system would be able to provide information on the spatial distributions of photosensitizer concentrations, tissue oxygenation, and delivered light dose, all while monitoring the photobleaching dynamics of the photosensitizer. Although the concept behind the combined system is not specific to any one photosensitizer, we focused on designing the system for the endogenous PDT of Gram-positive bacteria which utilizes coproporphyrin III as the photosensitizer.
The overall performance of the system was assessed, with the accuracy, precision, and resolution of the SFDI-derived optical property maps being determined to fall within comparable ranges to other systems, despite the spatial frequency utilized for the shorter wavelengths. After validating the ability of the system to correct for tissue-like optical properties, and thus produce accurate quantitative fluorescence images, a preliminary assessment of antimicrobial PDT photobleaching dosimetry was performed, and high correlations were found between the fluorescence and PDT outcomes.
Overall, the developed imaging system showcases the potential to enable a more thorough analysis of PDT dosimetry and the impact of different variables on treatment outcomes.
目前用于光动力疗法(PDT)剂量测定的方法已被证明存在不足,因为它们无法在不中断PDT治疗的情况下提供准确、实时和空间分辨的监测。
我们的目标是开发并验证一种联合治疗和剂量测定系统,该系统能够在非接触式PDT过程中实时监测隐式和显式剂量测定。
通过采用荧光成像和空间频域成像(SFDI),并使用低成本的现成组件进行设计,该联合成像系统将能够提供有关光敏剂浓度、组织氧合和输送光剂量的空间分布信息,同时监测光敏剂的光漂白动力学。尽管联合系统背后的概念并非特定于任何一种光敏剂,但我们专注于为利用粪卟啉III作为光敏剂的革兰氏阳性菌内源性PDT设计该系统。
评估了系统的整体性能,确定SFDI衍生的光学特性图的准确性、精密度和分辨率与其他系统在可比范围内,尽管较短波长使用的空间频率有所不同。在验证了系统校正类组织光学特性从而产生准确的定量荧光图像的能力后,对抗菌PDT光漂白剂量测定进行了初步评估,发现荧光与PDT结果之间存在高度相关性。
总体而言,开发的成像系统展示了更全面分析PDT剂量测定以及不同变量对治疗结果影响的潜力。