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一种用于肿瘤成像和光疗的双功能光敏剂的新方法。

A novel approach to a bifunctional photosensitizer for tumor imaging and phototherapy.

作者信息

Chen Yihui, Gryshuk Amy, Achilefu Samuel, Ohulchansky Tymish, Potter William, Zhong Tuoxiu, Morgan Janet, Chance Britton, Prasad Paras N, Henderson Barbara W, Oseroff Allan, Pandey Ravindra K

机构信息

PDT Center, Cell Stress Biology, Roswell Park Cancer Institute, Buffalo, New York 14263, USA.

出版信息

Bioconjug Chem. 2005 Sep-Oct;16(5):1264-74. doi: 10.1021/bc050177o.

Abstract

Optical imaging has attracted a great attention for studying molecular recognitions because minute fluorescent tracers can be detected in homogeneous and heterogeneous media with existing laboratory instruments. In our preliminary study, a clinically relevant photosensitizer (HPPH, a chlorophyll-a analog) was linked with a cyanine dye (with required photophysical characteristics but limited tumor selectivity), and the resulting conjugate was found to be an efficient tumor imaging (fluorescence imaging) and photosensitizing agent. Compared to HPPH, the presence of the cyanine dye moiety in the conjugate produced a significantly higher uptake in tumor than skin. At a therapeutic/imaging dose, the conjugate did not show any significant skin phototoxicity, a major drawback associated with most of the porphyrin-based photosensitizers. These results suggest that tumor-avid porphyrin-based compounds can be used as "vehicles" to deliver the desired fluorescent agent(s) to tumor. The development of tumor imaging or improved photodynamic therapy agent(s) by itself represents an important step, but a dual function agent (fluorescence imaging and photodynamic therapy) provides the potential for tumor detection and targeted photodynamic therapy, combining two modalities into a single cost-effective "see and treat" approach.

摘要

光学成像因能利用现有实验室仪器在均相和非均相介质中检测微量荧光示踪剂,在研究分子识别方面备受关注。在我们的初步研究中,一种临床相关的光敏剂(HPPH,一种叶绿素 - a类似物)与一种菁染料(具有所需的光物理特性但肿瘤选择性有限)相连,结果发现所得的共轭物是一种有效的肿瘤成像(荧光成像)和光致敏剂。与HPPH相比,共轭物中菁染料部分的存在使其在肿瘤中的摄取量显著高于皮肤。在治疗/成像剂量下,该共轭物未表现出任何明显的皮肤光毒性,而这是大多数基于卟啉的光敏剂的主要缺点。这些结果表明,基于卟啉的亲肿瘤化合物可作为“载体”,将所需的荧光剂递送至肿瘤。开发肿瘤成像或改进的光动力治疗剂本身就是重要的一步,但双功能剂(荧光成像和光动力治疗)为肿瘤检测和靶向光动力治疗提供了潜力,将两种模式结合成一种经济高效的“可视即治疗”方法。

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