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首页> 外文期刊>Methods and findings in experimental and clinical pharmacology >Initiation of apoptosis by photodynamic therapy using a novel positively charged and water-soluble near infra-red photosensitizer and white light irradiation.
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Initiation of apoptosis by photodynamic therapy using a novel positively charged and water-soluble near infra-red photosensitizer and white light irradiation.

机译:通过使用新型带正电且水溶性的近红外光敏剂和白光照射的光动力疗法启动细胞凋亡。

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摘要

Our aim was to investigate the photophysical and photodynamic properties of a new, water-soluble positively charged and chemicaly stable photosensitizer: tetrahydroporphyrin tetratosylat (THPTS). Absorption, fluorescence and (1)H NMR spectra and the intracellular distribution of THPTS were measured. The apoptosis in choroidal melanoma cells was measured using cell death detection ELISA and caspase-8 activity assay. THPTS-PDT efficiency was studied in Balb/c mice bearing C26 colon carcinoma. Subcutaneously located tumors were irradiated with a white light source at a fluence rate of 100 mW/cm(2). THPTS was administrated 3 h before illumination. The tumoricidal effect was examined 24 h after THPTS-PDT by vital staining with 0.4-ml 1% Evans blue solution, intrapertonially injected to each mouse. THPTS showed a strong absorption band at 760 nm. Its purity, measured by (1)H NMR, is better than 99%. At 24-h incubation period, CLSM revealed THPTS fluorescence in mitochondria and cell nucleus. THPTS possesses no toxic effect in preincubated CM cells without irradiation, and THPTS-PDT causes efficient apoptosis. THPTS-PDT using white light irradiation at a dose of 480 J/cm(2) caused necrosis with a depth of 8 mm in subcutaneously located C26 colon carcinoma in Balb/c-mice. In accordance with the present results, the THPTS seems to be of interest for further in vivo investigations with broad-band white light sources. (c) 2008 Prous Science, S.A.U. or its licensors. All rights reserved.
机译:我们的目的是研究一种新型的水溶性带正电荷且化学稳定的光敏剂:四氢卟啉四甲苯磺酸盐(THPTS)的光物理和光动力学性质。测量了THPTS的吸收,荧光和(1)H NMR光谱以及细胞内分布。使用细胞死亡检测ELISA和caspase-8活性测定法测量脉络膜黑色素瘤细胞的凋亡。在携带C26结肠癌的Balb / c小鼠中研究了THPTS-PDT的效率。皮下定位的肿瘤以100 mW / cm(2)的注量速率用白光源照射。在光照前3小时施用THPTS。在THPTS-PDT后24小时,通过腹膜内注射给每只小鼠的0.4 ml 1%Evans蓝溶液进行活体染色,检查其杀肿瘤作用。 THPTS在760 nm处显示出很强的吸收带。通过(1)1 H NMR测得的纯度高于99%。潜伏期为24小时,CLSM在线粒体和细胞核中显示THPTS荧光。 THPTS在未经辐射的预培养CM细胞中没有毒性作用,THPTS-PDT导致有效的细胞凋亡。使用480 J / cm(2)剂量的白光照射的THPTS-PDT在Balb / c-小鼠皮下定位的C26结肠癌中引起8 mm深度的坏死。根据目前的结果,THPTS似乎对宽带白光源的进一步体内研究很感兴趣。 (c)2008年Prous Science,S.A.U。或其许可人。版权所有。

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