Department of Civil and Environmental Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Water Res. 2010 May;44(10):3121-32. doi: 10.1016/j.watres.2010.03.002. Epub 2010 Mar 6.
Previous work demonstrates that widely used fluoroquinolone antibacterial agents, including ciprofloxacin, are degraded by means of aqueous ultraviolet photolytic and titanium dioxide (TiO(2)) photocatalytic (using both ultraviolet-A (UVA) and visible light (Vis) irradiation) treatment processes. In this study, we investigate the effects of photolytic and photocatalytic treatment processes on the antibacterial activity of ciprofloxacin solutions under controlled laboratory conditions. In agreement with earlier work, rates of ciprofloxacin degradation under comparable solution conditions (100microM ciprofloxacin, 0 or 0.5g/L TiO(2), pH 6, 25 degrees C) follow the trend UVA-TiO(2)>Vis-TiO(2)>UVA. Release of ammonia and fluoride ions is observed and a range of organic products have been identified with liquid chromatography-tandem mass spectrometry. However, the identified organic products all appear to retain the core quinolone structure, raising concerns about residual antibacterial potency of the treated solutions. Quantitative microbiological assays with a reference Escherichia coli strain indicate that the antimicrobial potency of ciprofloxacin solutions track closely with the undegraded ciprofloxacin concentration during photolytic or photocatalytic reactions. Quantitative analysis shows that for each mole of ciprofloxacin degraded, the antibacterial potency of irradiated solutions decreases by approximately one "mole" of activity relative to that of the untreated ciprofloxacin solution. This in turn indicates that the ciprofloxacin photo(cata)lytic transformation products retain negligible antibacterial activity relative to the parent compound. The energy demands for achieving one order of magnitude reduction in antibacterial activity within the experimental system are estimated to be 175J/cm(2) (UVA-only), 29J/cm(2) (Vis-TiO(2)), and 20J/cm(2) (UVA-TiO(2)), which indicates that the UVA-TiO(2) photocatalysis is the most energy efficient process for achieving ciprofloxacin inactivation under laboratory conditions.
先前的研究表明,包括环丙沙星在内的广泛使用的氟喹诺酮类抗菌剂可通过水相紫外光解和二氧化钛(TiO(2))光催化(使用紫外-A(UVA)和可见光(Vis)照射)处理过程进行降解。在这项研究中,我们在受控的实验室条件下研究了光解和光催化处理过程对环丙沙星溶液抗菌活性的影响。与早期的研究结果一致,在相似的溶液条件下(100μM 环丙沙星、0 或 0.5g/L TiO(2)、pH 值 6、25℃),环丙沙星的降解速率遵循 UVA-TiO(2)>Vis-TiO(2)>UVA 的趋势。观察到氨和氟化物离子的释放,并通过液相色谱-串联质谱鉴定了一系列有机产物。然而,所鉴定的有机产物似乎都保留了核心喹诺酮结构,这引起了对处理后溶液残留抗菌效力的关注。使用参考大肠杆菌菌株的定量微生物测定表明,在光解或光催化反应中,环丙沙星溶液的抗菌效力与未降解的环丙沙星浓度密切相关。定量分析表明,每降解 1 摩尔环丙沙星,辐照溶液的抗菌效力相对于未处理的环丙沙星溶液降低约 1“摩尔”活性。这反过来表明,环丙沙星光(催化)转化产物相对于母体化合物保留了可忽略不计的抗菌活性。估计在实验系统中实现抗菌活性降低一个数量级所需的能量需求分别为 175J/cm(2)(仅 UVA)、29J/cm(2)(Vis-TiO(2))和 20J/cm(2)(UVA-TiO(2)),这表明 UVA-TiO(2)光催化是在实验室条件下实现环丙沙星失活的最节能过程。