首页> 外文期刊>Investigative ophthalmology & visual science >Phototoxicity of indocyanine green and brilliant blue G under continuous fluorescent illumination on cultured human retinal pigment epithelial cells
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Phototoxicity of indocyanine green and brilliant blue G under continuous fluorescent illumination on cultured human retinal pigment epithelial cells

机译:连续荧光照射下吲哚菁绿和艳蓝G对培养的人视网膜色素上皮细胞的光毒性

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PURPOSE. We compared the phototoxicity of indocyanine green (ICG) and Brilliant Blue G (BBG) in cultured RPE cells under fluorescent lamp illumination imitating ambient light. METHODS. Cultured human RPE line cells were stained with ICG or BBG solution at concentrations of clinical use, and cultured in a colorless medium for 24 hours in the dark or under illumination from a fluorescent lamp. After culture, cell morphology and TUNEL-positive apoptotic cells were observed. Cell viability and cell death rate were evaluated. Absorption spectral changes of BBG before and after incubation were measured. RESULTS. ICG-stained cells cultured under illumination changed to an oval morphology with increased number of apoptotic cells, whereas ICG-stained cells cultured in the dark, and BBGstained cells cultured under illumination and dark conditions maintained a flat morphology without increase in apoptotic cells. Cell viability decreased and cell death rate increased only in cells stained by ICG followed by culture under illumination. Staining cells with ICG at one-tenth concentration of clinical usage induced no cytotoxicity after culture under illumination. Approximately 30% of total BBG retained in the stained cells was released into the culture supernatant after incubation for 24 hours. The absorption spectrum of BBG did not change after fluorescent light irradiation. CONCLUSIONS. Illumination with a fluorescent lamp caused cell death via apoptosis in ICG-exposed, but not in BBG-exposed cultured RPE cells. BBG may be a safer dye than ICG because of low light-induced cytotoxicity and rapid elution from stained cells.
机译:目的。我们比较了在模拟环境光的荧光灯照明下培养的RPE细胞中吲哚菁绿(ICG)和亮蓝G(BBG)的光毒性。方法。将培养的人RPE系细胞用临床浓度的ICG或BBG溶液染色,并在无色培养基中在黑暗中或在荧光灯照射下培养24小时。培养后,观察细胞形态和TUNEL阳性凋亡细胞。评价细胞活力和细胞死亡率。测量了孵育前后BBG的吸收光谱变化。结果。在光照下培养的ICG染色的细胞变为凋亡细胞数量增加的椭圆形形态,而在黑暗中培养的ICG染色的细胞和在光照和黑暗条件下培养的BBG染色的细胞保持平坦的形态而凋亡细胞没有增加。仅在ICG染色并随后在光照下培养的细胞中,细胞活力降低且细胞死亡率增加。用ICG染色浓度为临床使用浓度的十分之一的细胞在光照下培养后不会引起细胞毒性。温育24小时后,保留在染色细胞中的总BBG的约30%释放到培养上清液中。荧光照射后,BBG的吸收光谱没有变化。结论。荧光灯照射通过暴露于ICG的细胞凋亡导致细胞死亡,但没有暴露于BBG的培养RPE细胞。 BBG可能是比ICG更安全的染料,因为它的光诱导细胞毒性低,并且可以从染色细胞中快速洗脱。

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