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Pharmacokinetics of ciprofloxacin and fluocinolone acetonide otic solution in pediatric patients

机译:环丙沙星和氟轻松乙酮耳溶液在儿科患者中的药代动力学

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? 2022 Elsevier Inc.Purpose: To describe the pharmacokinetics (PK) of ciprofloxacin 0.3 and fluocinolone acetonide 0.025 otic solution (CIPRO+FLUO), ciprofloxacin 0.3 otic solution alone (CIPRO), and fluocinolone acetonide 0.025 otic solution alone (FLUO) administered into the middle ears of pediatric patients with Acute Otitis Media with Tympanostomy Tubes (AOMT). Materials and methods: We performed a PK analysis of patients who participated in two multicenter, randomized, double-blind AOMT clinical trials (SALVAT studies CIFLOTIII/10IA02 and CIFLOTIII/10IA04). Each patient received 0.25 mL of CIPRO+FLUO, CIPRO, or FLUO twice a day instilled into the ear canal(s) for 7 days to treat AOMT. Blood samples of patients with unilateral AOMT were collected before the administration of the first dose of study medication at Visit 1 (day 1) and within 1–2 h after the last dose on day 7. Blood samples were analyzed to detect ciprofloxacin and fluocinolone acetonide concentrations using two validated liquid chromatography-tandem mass spectrometry (LC-MS-MS) methods, with the lower limit of quantification for ciprofloxacin and fluocinolone acetonide in plasma samples being 1 ng/mL. Thirty randomly selected patients between 10 months and 10 years of age (mean age, 4.4 years) were included in the study. Although all available samples were analyzed, only PK data of the 22 patients with both samples and unilateral disease were considered for study purposes. Results: No detectable concentrations of ciprofloxacin or fluocinolone acetonide in plasma were observed (<1 ng/mL). Conclusions: These results demonstrated negligible systemic exposure to ciprofloxacin and fluocinolone acetonide following topical otic administration in pediatric patients with AOMT.
机译:?2022 Elsevier Inc.目的:描述环丙沙星 0.3% 和氟轻松乙酮 0.025% 耳溶液 (CIPRO+FLUO)、环丙沙星 0.3% 单独耳溶液 (CIPRO) 和氟轻松乙酮 0.025% 单独耳溶液 (FLUO) 给药到小儿急性中耳炎中耳的药代动力学 (PK) 鼓膜造瘘管 (AOMT)。材料和方法:我们对参加两项多中心、随机、双盲 AOMT 临床试验(SALVAT 研究 CIFLOTIII/10IA02 和 CIFLOTIII/10IA04)的患者进行了 PK 分析。每位患者每天两次接受 0.25 mL CIPRO+FLUO、CIPRO 或 FLUO,滴入耳道持续 7 天以治疗 AOMT。在第 1 次就诊(第 1 天)给药第一剂研究药物之前和第 7 天最后一次给药后 1-2 小时内收集单侧 AOMT 患者的血样。使用两种经验证的液相色谱-串联质谱 (LC-MS-MS) 方法分析血液样本以检测环丙沙星和氟轻松乙酮浓度,血浆样本中环丙沙星和氟轻松乙酮的定量下限为 1 ng/mL。该研究纳入了30名随机选择的10个月至10岁(平均年龄为4.4岁)的患者。尽管分析了所有可用样本,但仅考虑了 22 名同时具有样本和单侧疾病的患者的 PK 数据用于研究目的。结果:血浆中未观察到环丙沙星或氟轻松乙酮的可检测浓度(<1 ng/mL)。结论:这些结果表明,AOMT儿科患者局部耳科给药后,环丙沙星和氟轻松乙酮的全身暴露可忽略不计。

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