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630纳米脉冲激光照射对血卟啉(®)介导的光动力疗法中HeLa细胞增殖的影响

Effect of 630-NM pulsed laser irradiation on the proliferation of HeLa cells in Photofrin(®)-mediated photodynamic therapy.

作者信息

Miyamoto Yuichi, Nishikiori Daisuke, Hagino Fumika, Wakita Masayoshi, Tanabe Ichiro, Toida Masahiro

机构信息

Faculty of Health and Medical Care, Saitama Medical University, Saitama 350-1241, Japan.

出版信息

Laser Ther. 2011;20(2):135-8. doi: 10.5978/islsm.20.135.

Abstract

BACKGROUND AND AIMS

Red laser light of wavelength 630 nm is usually used for Photofrin(®)-mediated photodynamic therapy (PDT). The 630-nm light employed in PDT corresponds to the region of the wavelength used in low-level laser therapy (LLLT) may influence on the photodynamic effect required for killing cancer cells. The aim of this in vitro study was to investigate the changes in cell viability and degree of cell proliferation after Photofrin(®)-mediated PDT using 630-nm pulsed laser irradiation (10 Hz repetition rate and 7-9 ns pulse width), which was clinically found to induce no remarkable cell injury.

MATERIALS AND METHODS

A study has been conducted in which HeLa cells are incubated with Photofrin(®) for 15 min (10 µg/ml). Irradiation was carried out at an average fluence rate of 50 mW/cm(2) with light doses of 1, 3, and 5 J/cm(2). The cytotoxic effects on the cells are evaluated by the XTT (2,3-bis[2-methoxy-4-nitro-5-sulfophenyl]-5-[(phenylamino)carbonyl]-2H-tetrazolium hydroxide) assay.

RESULTS

The results showed that the laser irradiated cells exhibited a greater clonogenic activity than normal and PDT treated cells for a short period after the laser irradiation.

CONCLUSION

If the level of 630-nm pulsed laser irradiation employed in a PDT is comparatively lowered, it would have a biostimulatory effect like that of in LLLT.

摘要

背景与目的

波长630nm的红色激光通常用于卟啉钠介导的光动力疗法(PDT)。PDT中使用的630nm光对应于低强度激光疗法(LLLT)中使用的波长区域,可能会影响杀死癌细胞所需的光动力效应。本体外研究的目的是调查使用630nm脉冲激光照射(重复频率10Hz,脉冲宽度7 - 9ns)进行卟啉钠介导的PDT后细胞活力和细胞增殖程度的变化,临床研究发现该照射不会引起明显的细胞损伤。

材料与方法

进行了一项研究,将HeLa细胞与卟啉钠孵育15分钟(10μg/ml)。以50mW/cm²的平均通量率,分别给予1、3和5J/cm²的光剂量进行照射。通过XTT(2,3 - 双[2 - 甲氧基 - 4 - 硝基 - 5 - 磺基苯基] - 5 - [(苯基氨基)羰基] - 2H - 四唑氢氧化合物)测定法评估对细胞的细胞毒性作用。

结果

结果表明,激光照射后的细胞在短时间内比正常细胞和接受PDT处理的细胞表现出更高的克隆形成活性。

结论

如果PDT中使用的630nm脉冲激光照射水平相对降低,它将具有类似于LLLT的生物刺激作用。

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