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首页> 外文期刊>Journal of aerosol medicine and pulmonary drug delivery >Evaluation of in vitro and in vivo flow rate dependency of budesonide/formoterol easyhaler?
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Evaluation of in vitro and in vivo flow rate dependency of budesonide/formoterol easyhaler?

机译:评价布地奈德/福莫特罗easyhaler的体外和体内流速依赖性?

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摘要

Methods: Inspiratory flow parameters via EH and Symbicort? Turbuhaler? (TH) inhalers were evaluated in 187 patients with asthma and COPD. The 10th, 50th, and 90thpercentile flow rates achieved by patients were utilized to study in vitro flow rate dependency of budesonide/formoterol EH and Symbicort TH. In addition, an exploratory pharmacokinetic study on pulmonary deposition of active substances for budesonide/formoterol EH in healthy volunteers was performed.Results: Mean inspiratory flow rates through EH were 64 and 56 L/min in asthmatics and COPD patients, and through TH 79 and 72 L/min, respectively. Children with asthma had marginally lower PIF values than the adults. The inspiratory volumes were similar in all groups between the inhalers. Using weighted 10th, 50th, and 90thpercentile flows the in vitro delivered doses (DDs) and fine particle doses (FPDs) for EH were rather independent of flow as 98% of the median flow DDs and 89%-93% of FPDs were delivered already at 10thpercentile air flow. Using±15% limits, EH and TH had similar flow rate dependency profiles between 10thand 90thpercentile flows. The pharmacokinetic study with budesonide/formoterol EH in healthy subjects (n=16) revealed a trend for a flow-dependent increase in lung deposition for both budesonide and formoterol.Conclusions: Comparable in vitro flow rate dependency between budesonide/formoterol EH and Symbicort TH was found using the range of clinically relevant flow rates. The results of the pharmacokinetic study were in accordance with the in vitro results showing only a trend of flow rate-dependant increase in lung deposition of active substances with EH.Background: The Easyhaler? (EH) device-metered dry powder inhaler containing budesonide and formoterol is being developed for asthma and chronic obstructive pulmonary disease (COPD). As a part of product optimization, a series of in vitro and in vivo studies on flow rate dependency were carried out.
机译:方法:通过EH和Symbicort吸气流量参数?涡轮增压器?在187例哮喘和COPD患者中评估了(TH)吸入器。将患者获得的第10、50和90%的流速用于研究布地奈德/福莫特罗EH和Symbicort TH的体外流速依赖性。此外,在健康志愿者中进行了布地奈德/福莫特罗EH活性物质肺部沉积的探索性药代动力学研究。结果:哮喘患者和COPD患者通过EH的平均吸气流速分别为64和56 L / min,通过TH 79和分别为72 L / min。哮喘患儿的PIF值略低于成年人。吸入器之间所有组的吸气量相似。使用加权的10%,50%和90%百分位流量,EH的体外递送剂量(DDs)和细颗粒剂量(FPDs)与流量无关,因为已经有98%的中位数DDs和89%-93%的FPD递送了空气流量为10%。在±15%的限制范围内,EH和TH在10%和90%的流量之间具有相似的流速依赖性曲线。布地奈德/福莫特罗EH在健康受试者中的药代动力学研究(n = 16)显示了布地奈德和福莫特罗的肺部血流依赖性增加趋势。结论:布地奈德/福莫特罗EH与Symbicort TH的体外流速依赖性相当使用临床相关流速范围发现。药代动力学研究的结果与体外结果一致,结果表明,EH活性物质在肺部沉积的速率仅依赖流速增加。趋势:Easyhaler? (EH)设备计量的含有布地奈德和福莫特罗的干粉吸入器正在开发中,用于治疗哮喘和慢性阻塞性肺疾病(COPD)。作为产品优化的一部分,进行了一系列有关流速依赖性的体外和体内研究。

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