Dartmouth College, Thayer School of Engineering, Hanover, New Hampshire, United States.
Massachusetts General Hospital, Harvard Medical School, Wellman Center for Photomedicine, Boston, Ma, United States.
J Biomed Opt. 2019 Dec;25(6):1-13. doi: 10.1117/1.JBO.25.6.063802.
: While clinical treatment of actinic keratosis by photodynamic therapy (PDT) is widely practiced, there is a well-known variability in response, primarily caused by heterogeneous accumulation of the photosensitizer protoporphyrin IX (PpIX) between patients and between lesions, but measurement of this is rarely done. : Develop a smartphone-based fluorescence imager for simple quantitative photography of the lesions and their PpIX levels that can be used in a new clinical workflow to guide the reliability of aminolevulinic acid (ALA) application for improved lesion clearance. : The smartphone fluorescence imager uses an iPhone and a custom iOS application for image acquisition, a 3D-printed base for measurement standardization, an emission filter for PpIX fluorescence isolation, and a 405-nm LED ring for optical excitation. System performance was tested to ensure measurement reproducibility and the ability to capture photosensitizer accumulation and photobleaching in pre-clinical and clinical settings. : PpIX fluorescence signal from tissue-simulating phantoms showed linear sensitivity in the 0.01 to 2.0 μM range. Murine studies with Ameluz® aminolevulinic acid (ALA) gel and initial human testing with Levulan® ALA cream verified that in-vivo imaging was feasible, including that PpIX production over 1 h is easily captured and that photobleaching from the light treatment could be quantified. : The presented device is the first quantitative wide-field fluorescence imaging system for PDT dosimetry designed for clinical skin use and for maximal ease of translation into clinical workflow. The results lay the foundation for using the system in clinical studies to establish treatment thresholds for the individualization of PDT treatment.
: 尽管光动力疗法(PDT)在临床上广泛用于治疗光化性角化病,但众所周知,其疗效存在很大的个体差异,主要是由于患者之间和病变之间的光敏剂原卟啉 IX(PpIX)的积累存在异质性,但很少进行这种测量。: 开发一种基于智能手机的荧光成像仪,用于对病变及其 PpIX 水平进行简单的定量摄影,该成像仪可用于新的临床工作流程,以指导氨基酮戊酸(ALA)应用的可靠性,从而提高病变清除率。: 智能手机荧光成像仪使用 iPhone 和定制的 iOS 应用程序进行图像采集,3D 打印的底座用于测量标准化,发射滤波器用于 PpIX 荧光分离,以及 405nm LED 环用于光学激发。对系统性能进行了测试,以确保测量的可重复性以及在临床前和临床环境中捕获光敏剂积累和光漂白的能力。: 组织模拟体中的 PpIX 荧光信号在 0.01 至 2.0 μM 范围内具有线性灵敏度。使用 Ameluz®氨基酮戊酸(ALA)凝胶进行的小鼠研究和使用 Levulan®ALA 乳膏进行的初步人体测试证实,体内成像是可行的,包括在 1 小时内很容易捕获 PpIX 的产生,并且可以量化来自光疗的光漂白。: 所提出的设备是第一个用于 PDT 剂量测定的临床皮肤使用的定量宽场荧光成像系统,旨在最大程度地简化其转化为临床工作流程。这些结果为在临床研究中使用该系统建立个体化 PDT 治疗的治疗阈值奠定了基础。