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5-氨基乙酰丙酸光动力学疗法杀伤人结肠癌两个细胞株的对比研究 被引量:2

Effect of 5-Aminolevulinic Acid(5-ALA)Mediated Photodynamic Therapy on Human Colon Carcinoma Cell Lines LoVo and CoLo205 in vitro
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摘要 目的探讨5-氨基乙酰丙酸(5-ALA)光动力学疗法(photodynamic therapy,PDT)对体外培养人结肠癌LoVo和CoLo205细胞的生物作用。方法于体外培养的LoVo和CoLo205细胞分别加入不同浓度的5-ALA(0.1、0.5、1.0、1.5、2.0和2.5 mmol/L)孵育6 h,以波长为630 nm的半导体激光进行照射,照射的功率密度为20mW/cm^2,照射能量密度分别为2、5、10、20 J/cm^2,继续孵育24h,用四唑盐(MTT)比色法测定细胞存活率;荧光分光光度计检测LoVo与CoLo205细胞内PpⅨ荧光强度。结果5-ALA-PDT对体外培养的人结肠癌LoVo和CoLo205细胞均有杀伤作用,两者无显著性差异(P>0.05)。其杀伤作用大小与5-ALA的浓度和激光剂量成正相关(P<0.01)。激光能量为20 J/cm^2,5-ALA的浓度为1.0 mmol/L时,其杀伤LoVo、CoLo205细胞的作用最明显;LoVo与CoLo205细胞内PpⅨ荧光强度差异无显著性意义(P>0.05)。结论5-ALA-PDT可有效杀伤体外培养的人结肠癌LoVo和CoLo205细胞,且对两种细胞的杀伤作用无显著性差异。 Objective To investigate the potential use of 5-aminolevulinic acid (5-ALA)-photodynamic therapy (PDT) of colon carcinoma cell lines LoVo and CoLo205 cultured in vitro. Methods LoVo and CoLo205 cells cultured in vitro were incubated in a medium contained various concentrations of 5-ALA (0.1,0.5, 1.0,1.5,2. 0 or 2. 5 mmol/L) for 4 hours and illuminated with different light doses (2,5,10 or 20 J/cm^2 ) using a semiconductor laser at 630 nm. After 24 hour incubation with 5-ALA-PDT, the survival rate of LoVo and CoLo205 cells was analyzed by MTT assay. The cellular fluorescence intensities of PpⅨ in LoVo and CoLo205 were measured with a luminescence spectrometer. Results 5-ALA-PDT may effectively kill the LoVo and CoLo205 cells cultured in vitro,while the killing effect showed no significant difference between them( P 〉0.05 ). The killing degrees were positively correlated with the concentration of 5-ALA and the dosage of radiation. The cellular PpⅨ fluorescence intensities had no significant difference between the two kinds of cells. Conclusions 5-ALA-PDT may effectively kill the LoVo and CoLo205 cells cultured in vitro.
出处 《中国激光医学杂志》 CAS CSCD 2008年第3期162-165,共4页 Chinese Journal of Laser Medicine & Surgery
基金 中国临床肿瘤学科学基金(Y20050013)
关键词 结肠癌 5-氨基乙酰丙酸 光动力学疗法 Colon carcinoma 5-Aminolevulinic acid (5-ALA) Photodynamic therapy (PDT)
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参考文献7

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