Jung Yookyung, Nichols Alexander J, Klein Oliver J, Roussakis Emmanuel, Evans Conor L
Wellman Center for Photomedicine, Harvard Medical School, Massachusetts General Hospital, Boston, Massachusetts (USA).
Isr J Chem. 2012 Sep;52(8-9):728-744. doi: 10.1002/ijch.201200009. Epub 2012 Sep 13.
A major challenge in creating and optimizing therapeutics in the fight against cancer is visualizing and understanding the microscale spatiotemporal treatment response dynamics that occur in patients. This is especially true for photodynamic therapy (PDT), where therapeutic optimization relies on understanding the interplay between factors such as photosensitizer localization and uptake, in addition to light dose and delivery rate. In vitro 3D culture systems that recapitulate many of the biological features of human disease are powerful platforms for carrying out detailed studies on PDT response and resistance. Current techniques for visualizing these models, however, often lack accuracy due to the perturbative nature of the sample preparation, with light attenuation complicating the study of intact models. Optical coherence tomography (OCT) is an ideal method for the long-term, non-perturbative study of in vitro models and their response to PDT. Monitoring the response of 3D models to PDT by time-lapse OCT methods promises to provide new perspectives and open the way to cancer treatment methodologies that can be translated towards the clinic.
在对抗癌症的过程中,创建和优化治疗方法面临的一个主要挑战是可视化和理解患者体内发生的微观时空治疗反应动态。对于光动力疗法(PDT)来说尤其如此,在该疗法中,除了光剂量和给药速率外,治疗优化还依赖于了解诸如光敏剂定位和摄取等因素之间的相互作用。能够重现人类疾病许多生物学特征的体外3D培养系统是开展关于PDT反应和耐药性详细研究的强大平台。然而,由于样品制备具有干扰性,当前用于可视化这些模型的技术往往缺乏准确性,光衰减使完整模型的研究变得复杂。光学相干断层扫描(OCT)是对体外模型及其对PDT的反应进行长期、非干扰性研究的理想方法。通过延时OCT方法监测3D模型对PDT的反应有望提供新的视角,并为可转化至临床的癌症治疗方法开辟道路。