Zgadzaj Anna, Kornacka Joanna, Jastrzębska Anita, Parzonko Andrzej, Sommer Sylwester, Nałęcz-Jawecki Grzegorz
Department of Environmental Health Sciences, Medical University of Warsaw, Poland.
Department of Environmental Health Sciences, Medical University of Warsaw, Poland.
J Photochem Photobiol B. 2018 Jan;178:201-210. doi: 10.1016/j.jphotobiol.2017.11.011. Epub 2017 Nov 9.
The development of innovative solutions in photosafety of photolabile pharmaceutical products may help to reduce the adverse effects of these products, caused by light exposure. Providing new data in this area of study is particularly important in case of drugs applied topically on sensitive organs such as eyes. The main goal of this research is to investigate whether two potential excipients, namely: p-coumaric acid and benzophenone-4, affect the photodegradation, phototoxicity and photogenotoxicity of water solutions of four fluoroquinolones: ciprofloxacin, lomefloxacin, fleroxacin and clinafloxacin. We conducted a set of bioassays combined with the application of high-performance liquid chromatography and mass spectrometry techniques. The significant reduction of phototoxic and photogenotoxic abilities was evaluated in mixtures with ciprofloxacin and p-coumaric acid by using the umu test with Salmonella typhimurium TA1535/pSK1002, the methylthiazol tetrazolium reduction assay, and the micronucleus assay with the V79 cell line. In the bacterial assay the opposite effect was observed for the formulation with lomefloxacin and p-coumaric acid. This may be explained by the significant differences in the profile of the lomefloxacin photodegradation products. Further, the photoprotective and antiphotomutagenic abilities of ciprofloxacin mixed with benzophenone-4 were assessed. Promising results obtained in compositions with ciprofloxacin may be a basis for further research. Nevertheless, the increase in the DNA damage potential in mixtures with p-coumaric acid and two other antibiotics shows the importance of the safety evaluation of such innovative combinations.
开发对光不稳定的药物产品的光安全性创新解决方案,可能有助于减少这些产品因光照而产生的不良反应。在局部应用于眼睛等敏感器官的药物情况下,提供该研究领域的新数据尤为重要。本研究的主要目的是调查两种潜在的辅料,即对香豆酸和二苯甲酮 - 4,是否会影响四种氟喹诺酮类药物(环丙沙星、洛美沙星、氟罗沙星和克林沙星)水溶液的光降解、光毒性和光遗传毒性。我们进行了一系列生物测定,并结合应用高效液相色谱和质谱技术。通过使用鼠伤寒沙门氏菌TA1535/pSK1002的umu试验、甲基噻唑四氮唑还原试验以及V79细胞系的微核试验,评估了环丙沙星与对香豆酸混合物中光毒性和光遗传毒性能力大幅降低的情况。在细菌试验中,观察到洛美沙星与对香豆酸制剂有相反的效果。这可能是由于洛美沙星光降解产物的谱图存在显著差异。此外,评估了环丙沙星与二苯甲酮 - 4混合后的光保护和抗光致突变能力。环丙沙星组合物中获得的有前景的结果可能是进一步研究的基础。然而,对香豆酸与另外两种抗生素混合物中DNA损伤潜力的增加表明了评估此类创新组合安全性的重要性。