Wang Lai-Xing, Li Jian-Wei, Huang Jian-Yue, Li Jian-Hong, Zhang Li-Jun, O'Shea Donal, Chen Zhi-Long
Changhai Hospital, Shanghai, 201620, People's Republic of China.
Yiwu City Central Hospital, Zhejiang, 322000, People's Republic of China.
Tumour Biol. 2015 Sep;36(9):6839-47. doi: 10.1007/s13277-015-3395-1. Epub 2015 Apr 7.
Chlorin derivatives are promising photosensitive agents for photodynamic therapy (PDT) of tumors. The aim of the current study is to investigate the PDT therapeutic effects of a novel chlorin-based photosensitizer, meso-tetra[3-(N,N-diethyl)aminomethyl-4-methoxy]phenyl chlorin (TMPC) for gliomas in vitro and in vivo. Physicochemical characteristics of TMPC were recorded by ultraviolet visible spectrophotometer and fluorescence spectrometer. The rate of singlet oxygen generation of TMPC upon photo-excitation was detected by using 1,3-diphenylisobenzofuran (DPBF). The accumulation of TMPC in gliomas U87 MG cells was measured by fluorescence spectrometer. The efficiency of TMPC-PDT in vitro was analyzed by MTT assay and clonogenic assay. The biodistribution and clearance of TMPC were determined by fluorescence measuring. Human gliomas U87 MG tumor-bearing mice model was used to evaluate the antitumor effects of TMPC-PDT. TMPC shows a singlet oxygen generation rate of 0.05 and displays a characteristic long wavelength absorption peak at 653 nm (ε = 15,400). The accumulation of TMPC increased with the increase of incubation time. In vitro, PDT using TMPC and laser showed laser dose- and concentration-dependent cytotoxicity to U87 MG cells. In U87 MG tumor-bearing mice, TMPC-PDT significantly reduced the growth of the tumors. Both in vitro and in vivo, TMPC showed little dark toxicity. In vitro and in vivo studies, it found that TMPC has excellent antitumor activities. It suggests that TMPC is a potential photosensitizer of photodynamic therapy for cancer.
二氢卟吩衍生物是用于肿瘤光动力疗法(PDT)的有前景的光敏剂。本研究的目的是在体外和体内研究一种新型的基于二氢卟吩的光敏剂——中-四[3-(N,N-二乙基)氨基甲基-4-甲氧基]苯基二氢卟吩(TMPC)对胶质瘤的PDT治疗效果。通过紫外可见分光光度计和荧光光谱仪记录TMPC的物理化学特性。使用1,3-二苯基异苯并呋喃(DPBF)检测光激发后TMPC的单线态氧生成速率。通过荧光光谱仪测量TMPC在胶质瘤U87 MG细胞中的积累。通过MTT法和克隆形成试验分析TMPC-PDT在体外的效率。通过荧光测量确定TMPC的生物分布和清除情况。使用人胶质瘤U87 MG荷瘤小鼠模型评估TMPC-PDT的抗肿瘤效果。TMPC的单线态氧生成速率为0.05,并在653 nm处显示特征性的长波长吸收峰(ε = 15,400)。TMPC的积累随着孵育时间的增加而增加。在体外,使用TMPC和激光的PDT对U87 MG细胞显示出激光剂量和浓度依赖性细胞毒性。在U87 MG荷瘤小鼠中,TMPC-PDT显著抑制了肿瘤生长。在体外和体内,TMPC均显示出极低的暗毒性。在体外和体内研究中,发现TMPC具有优异的抗肿瘤活性。这表明TMPC是一种潜在的癌症光动力治疗光敏剂。