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超声动力与光动力效应对 MDA-MB-231 细胞的比较。

Comparison between sonodynamic and photodynamic effect on MDA-MB-231 cells.

机构信息

Key Laboratory of Medicinal Resources and Natural Pharmaceutical Chemistry, Ministry of Education, National Engineering Laboratory for Resource Developing of Endangered Chinese Crude Drugs in Northwest of China, College of Life Sciences, Shaanxi Normal University, Xi'an 710062, Shaanxi, China.

出版信息

J Photochem Photobiol B. 2013 Oct 5;127:182-91. doi: 10.1016/j.jphotobiol.2013.08.015. Epub 2013 Aug 31.

Abstract

Photodynamic therapy (PDT) and sonodynamic therapy (SDT) are therapeutic modalities for tumors. In this study we investigated the combined cytotoxic effect of 0.36W/cm(2) and 0.72W/cm(2) ultrasound with various Ce6 concentrations (1, 2, 5, 10μg/ml), and that of 1μg/ml Ce6 with different laser light dose (650nm; 10.4mW/cm(2); 0.3, 0.6, 1.2 and 2.5J/cm(2)) on MDA-MB-231 cells. Both high reactive oxygen species (ROS) production and a decline in mitochondrial membrane potential (MMP) were detected with high Ce6 concentrations (5 and 10μg/ml) combined with 0.72W/cm(2) ultrasound and 1.2, 2.5J/cm(2) laser light with 1μg/ml Ce6. In addition, cell membrane integrity was evaluated by using propidium iodide (PI), revealing membrane damage was aggravated with the increasing ultrasound intensity, but no significant difference on cell membrane integrity could be observed after PDT treatment. These results suggest ROS may play an important role both in SDT and PDT. Besides, mitochondria may be an initial target in PDT while SDT can cause multi-site damages in MDA-MB-231 cells.

摘要

光动力疗法(PDT)和声动力疗法(SDT)是肿瘤的治疗方式。在这项研究中,我们研究了 0.36W/cm(2) 和 0.72W/cm(2) 超声与不同 Ce6 浓度(1、2、5、10μg/ml)联合的细胞毒性作用,以及 1μg/ml Ce6 与不同激光光剂量(650nm;10.4mW/cm(2);0.3、0.6、1.2 和 2.5J/cm(2))对 MDA-MB-231 细胞的联合细胞毒性作用。高 Ce6 浓度(5 和 10μg/ml)与 0.72W/cm(2) 超声联合,以及 1μg/ml Ce6 与 1.2、2.5J/cm(2) 激光光联合,均检测到活性氧(ROS)的大量产生和线粒体膜电位(MMP)的下降。此外,通过使用碘化丙啶(PI)评估细胞膜完整性,结果表明随着超声强度的增加,细胞膜完整性受损加剧,但 PDT 处理后,细胞膜完整性没有明显差异。这些结果表明 ROS 可能在 SDT 和 PDT 中均发挥重要作用。此外,线粒体可能是 PDT 的初始靶标,而 SDT 可以在 MDA-MB-231 细胞中造成多部位损伤。

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