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用磺化铝酞菁(AlPcS(4))进行光动力疗法(PDT)后线粒体、内质网和肌动蛋白丝的分析

Analysis of mitochondria, endoplasmic reticulum and actin filaments after PDT with AlPcS(4).

作者信息

Ferreira S D R M, Tedesco A C, Sousa G, Zângaro R A, Silva N S, Pacheco M T T, Pacheco-Soares C

机构信息

Laboratory of Cellular and Tecidual Biology, Instituto de Pesquisa e Desenvolvimento, Universidade do Vale do Paraíba, Av. Shishima Hifumi 2911, 12244-000, São José dos Campos, SP, Brazil.

出版信息

Lasers Med Sci. 2004;18(4):207-12. doi: 10.1007/s10103-003-0282-6. Epub 2004 Jan 14.

Abstract

Photodynamic therapy (PDT) is a therapeutic modality for the treatment of tumors. This technique uses a visible light to activate a photosensitizer compounds, leading to a photo-oxidation process of biological tissue that can induce apoptosis or necrosis both in vivo and in vitro. However many of the cytotoxic effects remain an open question to be investigated. The cytotoxicity to specific cellular targets of classical photosensitizers used in the PDT in vitro has been analyzed in this work. The photosensitizing effects of Chloroaluminum Phthalocyanine Tetrasulfonate (AlPcS(4)) were studied on the mitochondria, cytoskeleton and endoplasmic reticulum of HeLa cells. The cells were irradiated with a diode laser (working at 670 nm; energy density of 4.5 J/cm(2 )and power density of 45 mW/cm(2)). The spectrofluorimetric analysis of the mitochondria showed changes in membrane potential. Cytoskeleton and endoplasmic reticulum showed basic alterations in distribution after PDT treatment, as an indicator of cellular death process.

摘要

光动力疗法(PDT)是一种治疗肿瘤的方法。该技术利用可见光激活光敏剂化合物,引发生物组织的光氧化过程,此过程在体内和体外均可诱导细胞凋亡或坏死。然而,许多细胞毒性作用仍是有待研究的开放性问题。在这项工作中,分析了光动力疗法中使用的经典光敏剂在体外对特定细胞靶点的细胞毒性。研究了四磺酸氯铝酞菁(AlPcS(4))对HeLa细胞线粒体、细胞骨架和内质网的光敏作用。用二极管激光(工作波长670nm;能量密度4.5J/cm²,功率密度45mW/cm²)照射细胞。线粒体的荧光光谱分析显示膜电位发生变化。细胞骨架和内质网在光动力疗法处理后显示出分布的基本改变,作为细胞死亡过程的指标。

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