Department of Otolaryngology, College of Medicine, University of Florida, Gainesville, Florida.
Otol Neurotol. 2023 Jun 1;44(5):520-524. doi: 10.1097/MAO.0000000000003867. Epub 2023 Apr 6.
Tetracyclines are less cytotoxic to tympanic membrane (TM) fibroblasts than quinolones.
Use of quinolone ear drops after tympanostomy tube placement and for acute otitis externa has been linked to an increased risk of TM perforation. This has been verified in animal models. Cell culture studies have shown quinolones to be highly toxic to TM fibroblasts. Tetracyclines are a potential alternative to quinolones as they have been used to treat acute otitis externa and are thought to be nontoxic to the inner ear. We aimed to determine if tetracyclines are cytotoxic to TM fibroblasts.
Human TM fibroblasts were treated with 1:10 dilutions of ofloxacin 0.3%, ciprofloxacin 0.3%, doxycycline 0.3 and 0.5%, minocycline 0.3 and 0.5%, tetracycline 0.3 and 0.5%, or dilute HCl (control), twice within 24 hours or four times within 48 hours. After 2 hours of treatment, cells were returned to growth media. Cells were observed with phase-contrast microscopy until cytotoxicity was measured.
Fibroblasts had lower survival with ciprofloxacin 0.3% and doxycycline 0.5% treatment compared with the control after 24 and 48 hours (all p < 0.0001). Fibroblasts treated with minocycline 0.5% had increased cell survival after 24 hours. Minocycline 0.3 and 0.5% showed increased TM fibroblast survival after 48 hours (all p < 0.0001). Phase-contrast images mirrored the cytotoxicity findings.
Tetracyclines are less toxic to cultured TM fibroblasts than ciprofloxacin. Fibroblast tetracycline toxicity is drug and dose specific. Minocycline shows the most promise for possible otic applications in which fibroblast toxicity is a concern.
与喹诺酮类药物相比,四环素对鼓膜(TM)成纤维细胞的细胞毒性更小。
在鼓室造口管放置和急性外耳炎后使用喹诺酮类滴耳液与 TM 穿孔风险增加有关。这在动物模型中得到了验证。细胞培养研究表明,喹诺酮类药物对 TM 成纤维细胞具有高度毒性。四环素是喹诺酮类药物的潜在替代品,因为它们已被用于治疗急性外耳炎,并且被认为对内耳无毒。我们旨在确定四环素是否对 TM 成纤维细胞具有细胞毒性。
用 1:10 稀释的氧氟沙星 0.3%、环丙沙星 0.3%、强力霉素 0.3%和 0.5%、米诺环素 0.3%和 0.5%、四环素 0.3%和 0.5%、或稀盐酸(对照)处理人 TM 成纤维细胞,24 小时内处理两次或 48 小时内处理四次。治疗 2 小时后,细胞返回生长培养基。用相差显微镜观察细胞,直到测量到细胞毒性。
与对照组相比,24 小时和 48 小时后,0.3%环丙沙星和 0.5%强力霉素处理的成纤维细胞存活率较低(均 p <0.0001)。24 小时后,用 0.5%米诺环素处理的成纤维细胞存活率增加。48 小时后,0.3%和 0.5%米诺环素显示出增加的 TM 成纤维细胞存活率(均 p <0.0001)。相差显微镜图像反映了细胞毒性结果。
与环丙沙星相比,四环素对培养的 TM 成纤维细胞的毒性较小。成纤维细胞的四环素毒性具有药物和剂量特异性。米诺环素在外耳应用中最有希望,因为成纤维细胞毒性是一个问题。