体外和体内5-ALA在血管内皮细胞中的光敏能力。

Changgeng yi xue za zhi Pub Date : 1999-06-01
C J Chang, S F Ma, F C Wei
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引用次数: 0

摘要

背景:本研究旨在探讨光动力治疗复杂性血管瘤的可行性。我们研究了光敏剂5-氨基乙酰丙酸(5-ALA)在体外和体内模型中的作用。方法:在微血管内皮细胞(MEC)培养体系中检测5-ALA的体外光敏活性。加入不同浓度的5-ALA, 630 nm光照射细胞。采用活/死法或乳酸脱氢酶(LDH)法测定MEC死亡百分率。通过测定鸡冠组织坏死的数量,研究了5-ALA辐照后630 nm光能剂量的变化对鸡冠组织坏死的影响。结果:浓度为35微克/毫升的5-ALA与波长为630 nm的100mw /cm2的激光照射组合,可使MEC培养体系中50%的细胞死亡。5-ALA剂量为200 mg/kg,功率密度为80 mW/cm2时,鸡冠组织损伤深度为362.5 +/- 27.6微米。在100mw /cm2和120mw /cm2下,梳子的损伤深度分别为732.5 +/- 29.1微米和792.5 +/- 36.0微米。结论:5-ALA对人MEC对激光照射的敏化是有效的。然而,在未来的临床研究中,应考虑不同解剖结构的吸收程度和组织破坏程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro and in vivo photosensitizing capabilities of 5-ALA in vascular endothelial cells.

Background: The object of our study is to evaluate the feasibility of photodynamic therapy for complicated hemangiomas. We studied the effect of the photosensitizing agent 5-aminolevulinic acid (5-ALA) in both in vitro and in vivo models.

Methods: The in vitro photosensitizing activity of 5-ALA was examined in a microvascular endothelial cell (MEC) culture system. 5-ALA was added in various concentrations and the cells were illuminated at 630 nm. The percentage of MEC killed was measured by either a Live/Dead assay or an lactate dehydrogenase (LDH) assay. The effect of varying the light energy dose delivered at 630 nm after the administration of 5-ALA was studied by determining the amount of necrosis produced in chicken combs.

Results: The combination of 5-ALA at a concentration of 35 micrograms/ml, and illumination by 100 mW/cm2 of laser light at 630 nm wavelength, caused 50% cell kill in the MEC culture system. Chicken combs of animals that received 200 mg/kg of 5-ALA and illumination at a power density of 80 mW/cm2 had a depth of injury of 362.5 +/- 27.6 microns upon histological examination. Those combs that received 100 or 120 mW/cm2 showed a depth of injury of 732.5 +/- 29.1 and 792.5 +/- 36.0 microns respectively.

Conclusion: 5-ALA is effective in sensitizing human MEC to laser illumination. However, the degree of absorption and tissue destruction in different anatomical structures should be considered in future clinical studies.

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