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从储雾罐中提取的气雾剂特征作为实际剂量的决定因素。

Aerosol profile extracted from spacers as a determinant of actual dose.

作者信息

Verbanck Sylvia, Vervaet Chris, Schuermans Daniël, Vincken Walter

机构信息

Academic Hospital, Vrije Universiteit Brussel, 1090 Brussels, Belgium.

出版信息

Pharm Res. 2004 Dec;21(12):2213-8. doi: 10.1007/s11095-004-7673-7.

Abstract

PURPOSE

We propose a novel method to evaluate the efficacy of a pressurized metered dose inhaler (pMDI) in combination with a spacer, by not only considering the total dose extractable from the spacer but also the dependence of dose on the volume available for aerosol inhalation.

METHODS

We studied volume-dependence of aerosol concentration during extraction from two commonly used plastic spacers (150 ml AerochamberPlus; 750 ml Volumatic) after a single puff of a 100 microg salbutamol pMDI (HFA-Ventolin), using laser photometric measurements.

RESULTS

After a delay of is in each spacer, the aerosol peak dose for AerochamberPlus was 2-fold that for Volumatic (p < 0.001), with the peak appearing well within the first 0.5 L even for the largest spacer. The opposite dose relationship is reached when considering total cumulative dose, which was 2-fold higher for Volumatic than for AerochamberPlus (p < 0.001); >95% of total cumulative dose was extracted well within 3 L for the largest spacer. The 2-fold cumulative dose relationship was confirmed by chemical assay on an absolute filter [AerochamberPlus: 21.4+/-3.2 (SD) microg; Volumatic: 43.8+/-9.1 (SD) microg].

CONCLUSIONS

Actual aerosol dose available to patients during inhalation via spacers can only be done on the basis of a quantification of aerosol peak dose and cumulative dose as a function of extracted volume.

摘要

目的

我们提出一种新方法来评估压力定量吸入器(pMDI)与储物罐联合使用的效果,该方法不仅考虑从储物罐中可提取的总剂量,还考虑剂量对可供气溶胶吸入的体积的依赖性。

方法

我们使用激光光度测量法,研究了在单次按压100微克沙丁胺醇pMDI(HFA-万托林)后,从两种常用塑料储物罐(150毫升AerochamberPlus;750毫升Volumatic)中提取气溶胶时气溶胶浓度的体积依赖性。

结果

在每个储物罐中都有延迟后,AerochamberPlus的气溶胶峰值剂量是Volumatic的2倍(p<0.001),即使对于最大的储物罐,峰值也出现在最初的0.5升内。考虑总累积剂量时,剂量关系相反,Volumatic的总累积剂量比AerochamberPlus高2倍(p<0.001);对于最大的储物罐,>95%的总累积剂量在3升内被很好地提取。通过绝对过滤器上的化学分析证实了2倍的累积剂量关系[AerochamberPlus:21.4±3.2(标准差)微克;Volumatic:43.8±9.1(标准差)微克]。

结论

通过储物罐吸入时患者实际可获得的气溶胶剂量,只能基于将气溶胶峰值剂量和累积剂量作为提取体积的函数进行量化来确定。

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