首页> 美国卫生研究院文献>Journal of Aerosol Medicine and Pulmonary Drug Delivery >In Vitro Characterization of the eFlow Closed System Nebulizer with Glycopyrrolate Inhalation Solution
【2h】

In Vitro Characterization of the eFlow Closed System Nebulizer with Glycopyrrolate Inhalation Solution

机译:格隆溴铵吸入溶液对eFlow封闭系统雾化器的体外表征

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>Background: Glycopyrrolate administered by a novel, investigational eFlow® Closed System (CS) nebulizer (eFlow CS) is being evaluated for the maintenance treatment of chronic obstructive pulmonary disease (COPD). The eFlow CS is a hand-held, vibrating membrane nebulizer optimized to deliver 1 mL of glycopyrrolate solution into the lung in <3 minutes. Clinical studies have shown improvements in lung function of subjects treated with nebulized glycopyrrolate.>Methods: The aerosol performance of the eFlow CS nebulizer was characterized by delivered dose, aerodynamic droplet size distribution and nebulization time. Simulated use nebulizer performance over 60 days was assessed by volume median diameter (VMD), nebulized amount, and nebulization time. Nebulization outputs were assayed to ensure adequate delivery of glycopyrrolate with an acceptable impurity profile. Aerosol condensates were analyzed for glycopyrrolate concentration and impurities by ultra-high-performance liquid chromatography and compared with non-nebulized samples.>Results: The mean mass median aerodynamic diameter, geometric standard deviation, and fine particle fraction were 3.7 μm, 1.7, and 72%, respectively, and independent of formulation strength (25 and 50 μg/mL). Delivered dose was 88% of the nominal dose for both formulation strengths. The mean delivered dose, assessed by breathing simulation, was 56.8% for 25 μg/mL and 62.6% for 50 μg/mL. Nebulization times were 1–2.5 minutes with no apparent increasing trend with use over a 60-day period. The nebulized amount showed no significant changes, whereas the VMD showed a slight, but not pharmaceutically relevant, increase (0.1–0.2 μm) after 60-day simulated use. Glycopyrrolate concentration and impurity levels of nebulized samples were statistically similar to those of non-nebulized samples.>Conclusion: The eFlow CS generates glycopyrrolate aerosols with high delivered dose, short treatment time, and small droplet size with narrow size distribution suitable for central and peripheral airway deposition. The unit dose vial mitigates medication misuse and ensures dose uniformity. Results support the use of glycopyrrolate/eFlow CS for the treatment of COPD.
机译:>背景:正在评估一种新型的研究性eFlow ®密闭系统(CS)雾化器(eFlow CS)雾化的格隆溴铵是否可用于慢性阻塞性肺疾病(COPD)的维持治疗。 eFlow CS是一款手持式振动膜雾化器,经过优化可在不到3分钟的时间内将1毫升的格隆溴铵溶液输送到肺中。临床研究表明,雾化的格隆溴铵治疗的受试者的肺功能有所改善。>方法: eFlow CS雾化器的气溶胶性能通过给药剂量,空气动力学液滴尺寸分布和雾化时间来表征。通过体积中值直径(VMD),雾化量和雾化时间评估60天内的模拟使用雾化器性能。分析雾化输出以确保以可接受的杂质分布充分递送格隆溴铵。通过超高效液相色谱法分析了气溶胶冷凝物中的格隆溴铵浓度和杂质,并与非雾化样品进行了比较。>结果:平均质量平均空气动力学直径,几何标准偏差和细颗粒分数为分别为3.7μm,1.7和72%,并且与制剂强度(25和50μg/ mL)无关。两种制剂强度的递送剂量均为标称剂量的88%。通过呼吸模拟评估的平均递送剂量对于25μg/ mL为56.8%,对于50μg/ mL为62.6%。雾化时间为1-2.5分钟,在60天的使用时间内没有明显的增加趋势。在模拟使用60天后,雾化的量没有显着变化,而VMD则有轻微的增加,但与药物无关,增加了(0.1-0.2μm)。雾化样品中的甘草检定浓度和杂质水平与非雾化样品在统计学上相似。>结论: eFlow CS产生了吡咯烷酸盐气雾剂,其递送剂量高,处理时间短,液滴尺寸小且尺寸窄适用于中央和周围气道沉积的分布。单位剂量的药水瓶可减轻药物滥用并确保剂量均匀性。结果支持使用格隆溴铵/ eFlow CS治疗COPD。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号