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Bioluminescence Monitoring of Photodynamic Therapy Response of Rat Gliosarcoma In Vitro and In Vivo

机译:体外和体内对大鼠脑胶质肉瘤光动力治疗反应的生物发光监测

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摘要

Photodynamic Therapy (PDT) is a promising modality for tumor treatment that combines a photosensitizing agent and visible light resulting in the production of cytotoxic reactive oxygen species leading to cell death. Bioluminescence detection/imaging is a noninvasive technique that uses luciferase gene transfection together with administration of luciferin to generate detectable visible light. It can provide real-time assessment of tumor growth and therapeutic response. The aim of this study is to investigate the potential of bioluminescence using in vitro and in vivo models to provide quantitative spatial and temporal information of brain tumor response (9L murine gliosarcoma) following animolevulinic acid (ALA)-mediated PDT. The in vitro results show a decrease of luminescence, with an excellent correlation to the number of viable cells. In vivo, the tumor growth was monitored using a cooled CCD camera, and ALA-PDT was performed 7-10 days post tumor implantation. The results show a decrease of the bioluminescence signal from the tumor that corresponds to a decrease of viable cells within the tumor, followed by re-growth at the sub-curative PDT doses used.
机译:光动力疗法(PDT)是一种有前途的肿瘤治疗方法,结合了光敏剂和可见光,可产生细胞毒性的活性氧,导致细胞死亡。生物发光检测/成像是一种非侵入性技术,使用萤光素酶基因转染并同时施用萤光素来产生可检测的可见光。它可以提供肿瘤生长和治疗反应的实时评估。这项研究的目的是研究使用体内和体外模型提供生物发光的潜力,以提供在乙酰氨基乙酰丙酸(ALA)介导的PDT后脑肿瘤反应(9L鼠类神经胶质肉瘤)的定量时空信息。体外结果显示发光减少,与存活细胞的数量具有极好的相关性。在体内,使用冷却的CCD照相机监测肿瘤的生长,并在肿瘤植入后7-10天进行ALA-PDT。结果显示来自肿瘤的生物发光信号的减少对应于肿瘤内存活细胞的减少,随后以所使用的亚治疗性PDT剂量重新生长。

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