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气溶胶颗粒大小并不能预测儿童药代动力学确定的肺部剂量。

Aerosol particle size does not predict pharmacokinetic determined lung dose in children.

机构信息

Copenhagen Prospective Studies on Asthma in Childhood, Danish Pediatric Asthma Center, Health Sciences, University of Copenhagen, Copenhagen University Hospital, Gentofte, Copenhagen, Denmark.

出版信息

J Clin Pharmacol. 2013 May;53(5):517-22. doi: 10.1002/jcph.74. Epub 2013 Mar 30.

Abstract

In vitro measures of aerosol particles size, such as the fine particle mass, play a pivotal role for approval of inhaled anti-asthmatic drugs. However, the validity as a measure of dose to the lungs in children lacks evidence. In this study we investigated for the first time the association between an in vivo estimate of lung dose of inhaled drug in children and the corresponding particle size segments assessed ex vivo. Lung dose of fluticasone propionate after inhalation from a dry powder inhaler (Diskus®) was studied in 23 children aged 4-7 and 12-15 years with mild asthma. Six-hour pharmacokinetics was assessed after single inhalation. The corresponding emitted mass of drug in segments of aerosol particle size was assessed ex vivo by replicating the inhalation flows recorded by transducers built into the Diskus® inhaler and re-playing them in a breathing simulator. There was no correlation between any inhaled particle size segment and lung dose assessed by pharmacokinetics and adjusted for age and body size. Measures of particles size segments were not related to lung dose in children. Until further evidence is provided it may be warranted to emphasize pharmacokinetic or pharmacodynamic assessments of drug delivery to the lung.

摘要

体外气溶胶颗粒大小的测量,如细颗粒质量,在批准吸入性抗哮喘药物方面起着关键作用。然而,作为儿童肺部剂量的测量手段的有效性缺乏证据。在这项研究中,我们首次研究了儿童吸入性药物的体内估计肺剂量与体外评估的相应颗粒大小段之间的关系。在 23 名年龄在 4-7 岁和 12-15 岁之间的轻度哮喘儿童中,使用干粉吸入器(碟式吸入器)吸入丙酸氟替卡松。单次吸入后进行 6 小时药代动力学评估。通过复制内置在碟式吸入器中的传感器记录的吸入流量并在呼吸模拟器中重新播放,在体外评估了相应的气溶胶颗粒大小段中的药物发射质量。任何吸入颗粒大小段与药代动力学评估的肺剂量之间均无相关性,且经年龄和体型校正后也是如此。颗粒大小段的测量与儿童的肺剂量无关。在提供进一步证据之前,强调对药物输送到肺部的药代动力学或药效学评估可能是合理的。

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