Horio T, Miyauchi H, Asada Y, Aoki Y, Harada M
Department of Dermatology, Kansai Medical University, Osaka, Japan.
J Dermatol Sci. 1994 Apr;7(2):130-5. doi: 10.1016/0923-1811(94)90086-8.
Clinical reports indicate that the fluoroquinolone group of antibiotics can induce cutaneous photosensitivity reactions. In the present study, phototoxicity and photoallergenicity of quinolones including nalidixic acid (NA) norfloxacin (NFLX), ofloxacin (OFLX), enoxacin (ENX), ciprofloxacin (CPFX), lomefloxacin (LFLX), and tosufloxacin (TFLX) were experimentally examined in an in vivo system using the guinea pig. Phototoxicity of all quinolones tested was demonstrated after a single, oral administration of the drugs and subsequent exposure to long-wave ultraviolet (UVA) at a dose of 30 J/cm2. The phototoxic potencies were: ENX, LFLX > OFLX > NA, TFLX > NFLX, CPFX. Photoallergic reaction was also induced to LFLX and NA by pretreatment with cyclophosphamide, an immunoadjuvant. No cross-reactions in photoallergy were observed among quinolones. The photo-ingestion test was positive in photoallergically sensitized animals, while the photopatch test was negative. This is the first report which demonstrated experimentally the photoallergenicity of quinolones. Clinical features of the photosensitivity due to quinolones can be explained by the results of the present experiments.
临床报告表明,氟喹诺酮类抗生素可引发皮肤光敏反应。在本研究中,使用豚鼠在体内系统中对包括萘啶酸(NA)、诺氟沙星(NFLX)、氧氟沙星(OFLX)、依诺沙星(ENX)、环丙沙星(CPFX)、洛美沙星(LFLX)和妥舒沙星(TFLX)在内的喹诺酮类药物的光毒性和光致敏性进行了实验研究。单次口服给药并随后以30 J/cm2的剂量暴露于长波紫外线(UVA)后,所测试的所有喹诺酮类药物均表现出光毒性。光毒性强度为:ENX、LFLX>OFLX>NA、TFLX>NFLX、CPFX。通过免疫佐剂环磷酰胺预处理,还可诱导对LFLX和NA产生光过敏反应。喹诺酮类药物之间未观察到光过敏交叉反应。光过敏致敏动物的光摄入试验呈阳性,而光斑贴试验呈阴性。这是第一份通过实验证明喹诺酮类药物光致敏性的报告。喹诺酮类药物引起的光敏反应的临床特征可以用本实验结果来解释。