Department of Ophthalmology, Örebro University Hospital, 701 85, Örebro, Sweden.
Graefes Arch Clin Exp Ophthalmol. 2013 Feb;251(2):509-14. doi: 10.1007/s00417-012-2176-4. Epub 2012 Oct 19.
To investigate whether ultraviolet light (UVA) at 365 nm can inhibit/eliminate Acanthamoeba growth and if riboflavin would potentiate such an association.
Acanthamoeba castellanii in a fluid medium with a concentration of approximately 1.7 × 10(4) protozoa/ml were prepared with (0.01 %) and without riboflavin. Exposure of UVA (dose 5.475 J/cm(2)) took place twice, with each illumination period followed by culturing of 10 μl in peptone yeast-extract glucose (PYG) medium for 7 days. Every suspension prepared had a non-exposed control solution. Determination of Acanthamoeba was conducted daily, by count in Burker chamber days 4 through 7 after exposure. Statistical analysis was done by repeated-measurement ANOVA and post-hoc analysis for unpaired samples.
The exposure of ultraviolet light resulted in an inhibited growth of Acanthamoeba compared to the non-exposed solutions, with a statistically significant reduction over time (p = 0.0003). The addition of riboflavin did not amplify the effect, and there were no tendencies for an interaction effect between UVA and riboflavin.
The antiprotozoal effect of the UVA wavelength, utilized in CXL, is solely mediated by ultraviolet light, and riboflavin does not seem to amplify the antimicrobial efficacy.
研究 365nm 紫外线(UVA)是否能抑制/消除棘阿米巴的生长,以及核黄素是否能增强这种作用。
用含有约 1.7×10(4)个原生动物/ml 的核黄素(0.01%)和不含核黄素的流体介质制备棘阿米巴 Castellanii。两次暴露于 UVA(剂量为 5.475J/cm(2)),每次光照后用 10μl 胰蛋白胨酵母提取物葡萄糖(PYG)培养基培养 7 天。每个悬液都有一个未经照射的对照溶液。在照射后第 4 天至第 7 天,每天通过布勒室计数来确定棘阿米巴的数量。采用重复测量方差分析和非配对样本的事后分析进行统计分析。
与未暴露的溶液相比,紫外线照射导致棘阿米巴的生长受到抑制,且随时间推移具有统计学意义(p=0.0003)。核黄素的添加并没有增强这种作用,而且 UVA 和核黄素之间也没有相互作用的趋势。
在 CXL 中使用的 UVA 波长的抗原生动物作用仅由紫外线介导,核黄素似乎不会增强其抗菌效果。