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布地奈德与福莫特罗干粉吸入剂组合在体外的吸入器内及吸入器间流速依赖性剂量释放

In-vitro intra- and inter-inhaler flow rate-dependent dosage emission from a combination of budesonide and eformoterol in a dry powder inhaler.

作者信息

Tarsin W, Assi K H, Chrystyn H

机构信息

School of Pharmacy, University of Bradford, Bradford BD7 1DP, United Kingdom.

出版信息

J Aerosol Med. 2004 Spring;17(1):25-32. doi: 10.1089/089426804322994433.

Abstract

Some dry powder inhalers have profound inhalation flow rate-dependent dosage emission, and it has been suggested that there are links between the in vitro emitted dose, total lung deposition, and subsequent clinical response. We have measured the in vitro dosage delivery for a combination of budesonide and eformoterol in a new version of the Turbuhaler. At inhalation flow rates of 30, 60, and 90 Lmin(-1), the total dose emission for 10 separate inhalations from each of six inhalers was determined. The aerodynamic characteristics of the emitted dose using inhalation flow rates of 28.3 and 60 Lmin(-1) were measured using the Andersen Cascade Impactor. The mean (SD) emitted dose for budesonide, at 30, 60, and 90 Lmin(-1), was 37.5%(18.2%), 64.4%(16.6%), and 107.4%(36.0%) (of the nominal emitted dose), respectively, and for eformoterol were 38.0%(20.3%), 65.0%(16.8%), and 104.9%(36.2%) (of the nominal emitted dose), respectively. Variability of dose emission characteristics from each inhaler and between inhalers at each flow rate was found. The aerodynamic particle size characterization of the emitted dose at flow rates of 28.3 and 60 Lmin(-1) revealed a mean fine particle dose for budesonide of 11.9% and 28.6% of the nominal emitted dose, respectively, and similarly 10.0% and 26.3% for eformoterol. At 28.3 Lmin(-1), the majority of the emitted dose (54.8% for budesonide and 64.5% for eformoterol) was deposited in the throat and preseparator of the Andersen Cascade Impactor. The mass median aerodynamic diameters for budesonide and eformoterol at 28.3 Lmin(-1) were 3.2 and 3.6 microm, respectively, and similarly at 60 Lmin(-1) were 2.4 and 2.5 microm. The modified Turbuhaler containing a budesonide and eformoterol combined formulation shows intra- and inter-inhaler flow-dependent dosage emission. The clinical significance of the in vitro dose-dependent properties should be investigated.

摘要

一些干粉吸入器的剂量释放与吸入流速密切相关,有人认为体外释放剂量、肺内总沉积量与后续临床反应之间存在联系。我们测量了新型都保装置中布地奈德和福莫特罗组合制剂的体外给药剂量。在吸入流速为30、60和90 Lmin(-1)时,测定了六个吸入器中每个吸入器10次单独吸入的总剂量释放。使用安德森级联撞击器测量了吸入流速为28.3和60 Lmin(-1)时释放剂量的空气动力学特性。布地奈德在30、60和90 Lmin(-1)时的平均(标准差)释放剂量分别为(标称释放剂量的)37.5%(18.2%)、64.4%(16.6%)和107.4%(36.0%),福莫特罗分别为38.0%(20.3%)、65.0%(16.8%)和104.9%(36.2%)。发现了每个吸入器以及不同吸入器在每个流速下剂量释放特性的变异性。在28.3和60 Lmin(-1)流速下释放剂量的空气动力学粒径特征显示,布地奈德的平均细颗粒剂量分别为标称释放剂量的11.9%和28.6%,福莫特罗同样分别为10.0%和26.3%。在28.3 Lmin(-1)时,大部分释放剂量(布地奈德为54.8%,福莫特罗为64.5%)沉积在安德森级联撞击器的喉部和预分离器中。布地奈德和福莫特罗在28.3 Lmin(-1)时的质量中值空气动力学直径分别为3.2和3.6微米,在60 Lmin(-1)时同样分别为2.4和2.5微米。含有布地奈德和福莫特罗联合制剂的改良都保装置显示出吸入器内和吸入器间流速依赖性剂量释放。体外剂量依赖性特性的临床意义应予以研究。

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