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首页> 外文期刊>Journal of aerosol medicine and pulmonary drug delivery >Validation of methodology for recording breathing and simulating drug delivery through spacers and valved holding chambers.
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Validation of methodology for recording breathing and simulating drug delivery through spacers and valved holding chambers.

机译:记录呼吸并模拟通过垫片和带阀保持室的药物输送方法的验证。

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BACKGROUND: Output from spacers (or valved holding chambers) is sensitive to changes in breathing pattern. Different spacers have unique characteristics that may influence breathing. A method used for breathing simulation, where the simulated breathing can be recorded on subjects while they are using spacers, may allow for more accurate in vitro estimation of drug delivery in specific populations, using specific spacers. METHODS: A flow chamber was used to record breathing while salbutamol was administered to two adult subjects through different spacers. Each subject performed a series of breathing patterns over a range of different inhalation volumes and flows. Salbutamol "inhaled" by subjects was captured on inspiratory filters and quantified by ultraviolet spectrophotometry. Recorded breathing patterns were simulated and ex vivo drug delivery was compared to in vitro drug delivery. Three equipment configurations were used to validate different aspects of the methodology. Configuration 1: breathing recorded by pneumotachometer placed directly between a human subject and the spacer. Breathing simulation performed with an identical setup. Configuration 2: spacer enclosed within a flow-chamber while breathing was recorded. Breathing simulation performed with an identical setup. Configuration 3: spacer enclosed in flow chamber to record breathing, but not when simulating breathing. In each configuration, the ex vivo and in vitro (simulated) filter doses were compared. RESULTS: Configuration 1: the median difference between ex vivo and in vitro filter doses was 0.4% (range: -12.2 to 6.9%). Configuration 2: the median difference was -2.3% (range: -9.0 to 5.0%). Configuration 3: the median difference was 1.7% (range: -11.5 to 3.9%). CONCLUSION: Our results indicate that in vitro simulated drug delivery using this method of recording using a flow chamber, closely approximates ex vivo total drug delivery. This technique allows for recording of breathing on patients while they are using spacers, with minimum increase in dead space or resistance, and no physical alteration in the patient-device interface.
机译:背景:垫片(或带阀的保持腔)的输出对呼吸模式的变化很敏感。不同的垫片具有可能影响呼吸的独特特征。一种用于呼吸模拟的方法,其中可以在使用间隔物的情况下在对象上记录模拟的呼吸,该方法可以允许使用特定的间隔物在特定人群中进行更准确的体外药物递送估计。方法:使用流动室记录呼吸,同时通过两个不同的垫片将沙丁胺醇施用于两名成年受试者。每个受试者在一系列不同的吸入量和流量下执行一系列呼吸模式。被受试者“吸入”的沙丁胺醇在吸气过滤器上捕获并通过紫外分光光度法定量。模拟记录的呼吸模式,并将离体药物递送与体外药物递送进行比较。使用三种设备配置来验证方法的不同方面。配置1:由气动转速计记录的呼吸直接置于人体和间隔物之间​​。以相同的设置执行呼吸模拟。配置2:记录呼吸时封闭在流动室内的垫片。以相同的设置执行呼吸模拟。配置3:封闭在流动室中的垫片记录呼吸,但在模拟呼吸时不记录。在每种配置中,比较了离体和体外(模拟)过滤器的剂量。结果:配置1:离体和体外过滤剂量之间的中位数差异为0.4%(范围:-12.2至6.9%)。配置2:中位数差异为-2.3%(范围:-9.0至5.0%)。配置3:中位数差异为1.7%(范围:-11.5至3.9%)。结论:我们的结果表明,使用这种使用流室记录的方法进行的体外模拟药物递送非常接近离体总药物递送。这项技术可以记录患者在使用间隔物时的呼吸情况,使死腔或阻力的增加降到最低,并且患者-设备界面不会发生物理变化。

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