Standish Beau A, Yang Victor X D, Munce Nigel R, Wong Kee Song Louis-Michel, Gardiner Geoffrey, Lin Annie, Mao Youxin I, Vitkin Alex, Marcon Norman E, Wilson Brian C
Department of Medical Biophysics, University of Toronto, Ontario Cancer Institute, Toronto, Ontario, Canada.
Gastrointest Endosc. 2007 Aug;66(2):326-33. doi: 10.1016/j.gie.2007.02.040.
Doppler optical coherence tomography (DOCT) is an imaging modality that allows assessment of the microvascular response during photodynamic therapy (PDT) and may be a powerful tool for treatment monitoring/optimization in conditions such as Barrett's esophagus (BE).
To assess the technical feasibility of catheter-based intraluminal DOCT for monitoring the microvascular response during endoluminal PDT in an animal model of BE.
Thirteen female Sprague-Dawley rats underwent esophagojejunostomy to induce enteroesophageal reflux for 35 to 42 weeks and the formation of Barrett's mucosa. Of these, 9 received PDT by using the photosensitizer Photofrin (12.5 mg/kg intravenous), followed by 635-nm intraluminal light irradiation 24 hours after drug administration. The remaining 4 surgical rats underwent light irradiation without Photofrin (controls). Another group of 5 normal rats, without esophagojejunostomy, also received PDT. DOCT imaging of the esophagus by using a catheter-based probe (1.3-mm diameter) was performed before, during, and after light irradiation in all rats.
Distinct microstructural differences between normal squamous esophagus, BE, and the transition zone between the 2 tissues were observed on DOCT images. Similar submucosal microcirculatory effects (47%-73% vascular shutdown) were observed during PDT of normal esophagus and surgically induced BE. Controls displayed no significant microvascular changes.
No apparent difference was observed in the PDT-induced vascular response between normal rat esophagus and the BE rat model. Real-time monitoring of PDT-induced vascular changes by DOCT may be beneficial in optimizing PDT dosimetry in patients undergoing this therapy for BE and other conditions.
多普勒光学相干断层扫描(DOCT)是一种成像方式,可用于评估光动力疗法(PDT)期间的微血管反应,并且可能是用于诸如巴雷特食管(BE)等病症的治疗监测/优化的有力工具。
评估基于导管的腔内DOCT在BE动物模型的腔内PDT期间监测微血管反应的技术可行性。
13只雌性斯普拉格-道利大鼠接受食管空肠吻合术以诱导肠食管反流35至42周并形成巴雷特黏膜。其中,9只大鼠通过使用光敏剂卟啉钠(12.5mg/kg静脉注射)接受PDT,给药后24小时进行635nm腔内光照射。其余4只手术大鼠在未使用卟啉钠的情况下接受光照射(对照)。另一组5只未进行食管空肠吻合术的正常大鼠也接受了PDT。在所有大鼠的光照射前、照射期间和照射后,使用基于导管的探头(直径1.3mm)对食管进行DOCT成像。
在DOCT图像上观察到正常鳞状食管、BE以及这两种组织之间的过渡区存在明显的微观结构差异。在正常食管和手术诱导的BE的PDT期间观察到类似的黏膜下微循环效应(血管关闭47%-73%)。对照组未显示出明显的微血管变化。
在正常大鼠食管和BE大鼠模型之间,未观察到PDT诱导的血管反应有明显差异。通过DOCT实时监测PDT诱导的血管变化可能有助于优化接受BE和其他病症此疗法的患者的PDT剂量测定。