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首页> 外文期刊>Ultrasonics sonochemistry >Sonodynamic therapy using water-dispersed TiO2-polyethylene glycol compound on glioma cells: Comparison of cytotoxic mechanism with photodynamic therapy
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Sonodynamic therapy using water-dispersed TiO2-polyethylene glycol compound on glioma cells: Comparison of cytotoxic mechanism with photodynamic therapy

机译:水分散型TiO2-聚乙二醇化合物对神经胶质瘤细胞的声动力疗法:光动力疗法对细胞毒性机制的比较

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摘要

Sonodynamic therapy is expected to be a novel therapeutic strategy for malignant gliomas. The titanium dioxide (TiO_2) nanoparticle, a photosensitizer, can be activated by ultrasound. In this study, by using water-dispersed TiO_2 nanoparticles, an in vitro comparison was made between the photodynamic and sonodynamic damages on U251 human glioblastoma cell lines. Water-dispersed TiO_2 nanoparticles were constructed by the adsorption of chemically modified polyethylene glycole (PEG) on the TiO _2 surface (TiO_2/PEG). To evaluate cytotoxicity, U251 monolayer cells were incubated in culture medium including 100 μg/ml of TiO_2/PEG for 3 h and subsequently irradiated by ultraviolet light (5.0 mW/cm~2) or 1.0 MHz ultrasound (1.0 W/cm~2). Cell survival was estimated by MTT assay 24 h after irradiation. In the presence of TiO_2/PEG, the photodynamic cytotoxic effect was not observed after 20 min of an ultraviolet light exposure, while the sonodynamic cytotoxicity effect was almost proportional to the time of sonication. In addition, photodynamic cytotoxicity of TiO_2/PEG was almost completely inhibited by radical scavenger, while suppression of the sonodynamic cytotoxic effect was not significant. Results of various fluorescent stains showed that ultrasound-treated cells lost their viability immediately after irradiation, and cell membranes were especially damaged in comparison with ultraviolet-treated cells. These findings showed a potential application of TiO_2/PEG to sonodynamic therapy as a new treatment of malignant gliomas and suggested that the mechanism of TiO_2/PEG mediated sonodynamic cytotoxicity differs from that of photodynamic cytotoxicity.
机译:声动力疗法有望成为恶性神经胶质瘤的一种新型治疗策略。可以通过超声活化光敏剂二氧化钛(TiO_2)纳米颗粒。在这项研究中,通过使用水分散的TiO_2纳米颗粒,对U251人胶质母细胞瘤细胞系的光动力和声动力损伤进行了体外比较。通过在TiO _2表面(TiO_2 / PEG)上吸附化学改性的聚乙二醇(PEG)来构建水分散的TiO_2纳米颗粒。为了评估细胞毒性,将U251单层细胞在包含100μg/ ml TiO_2 / PEG的培养基中孵育3小时,然后用紫外线(5.0 mW / cm〜2)或1.0 MHz超声波(1.0 W / cm〜2)照射。 。照射后24小时通过MTT测定估计细胞存活。在TiO_2 / PEG的存在下,紫外线照射20分钟后未观察到光动力细胞毒性作用,而声动力细胞毒性作用几乎与超声处理时间成正比。此外,自由基清除剂几乎完全抑制了TiO_2 / PEG的光动力细胞毒性,而对声动力细胞毒性作用的抑制作用并不明显。各种荧光染色的结果表明,经超声处理的细胞在照射后立即丧失了生存能力,并且与经紫外线处理的细胞相比,细胞膜尤其受到损害。这些发现表明,TiO_2 / PEG在声动力疗法中作为恶性神经胶质瘤的一种新疗法具有潜在的应用前景,并表明TiO_2 / PEG介导的声动力细胞毒性的机制不同于光动力细胞毒性。

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