Suppr超能文献

布地奈德 来自氢氟烷烃-134A定量吸入器的口服与吸入丙酸倍氯米松的相对生物利用度。

Beclomethasone relative availability of oral versus inhaled beclomethasone dipropionate from an HFA-134A metered dose inhaler.

作者信息

Soria I, Harrison L I, Machacek J H, Cline A C, Stampone P A

机构信息

Department of Pharmacokinetics and Drug Metabolism, St. Paul, MN 55144-1000, USA.

出版信息

Biopharm Drug Dispos. 1998 Jul;19(5):297-302. doi: 10.1002/(sici)1099-081x(199807)19:5<297::aid-bdd105>3.0.co;2-i.

Abstract

3M has formulated a new chlorofluorocarbon-free (CFC-free) beclomethasone dipropionate (BDP) metered-dose inhaler (MDI) with the use of the propellant HFA-134a (HFA). Lung deposition studies demonstrated that the HFA BDP MDI delivers to the lungs approximately 56% of the BDP dose (ex-adaptor), a substantially higher percentage than the 5-30% delivered by conventional CFC BDP MDIs. As new sensitive bioanalytical methods are becoming available to quantitate systemic levels of inhaled corticosteroids, pharmacokinetic evaluations are emerging as sensitive and reproducible methods that can be used as a complement to the data obtained from lung deposition studies to assess and compare the performance of MDIs. The present study was designed to determine the beclomethasone (BOH) availability of oral BDP relative to inhaled HFA BDP as a first step to alloy MDI product comparisons in the future. Forty mild asthmatic patients completed this open-label, randomized, single-dose, two-period crossover study. Each patient received an oral dose of BDP (0.2, 0.5, 1, 2 or 5 mg) in one period and an inhaled dose of BDP (0.2 or 0.8 mg) in the other period, with four patients allocated to each of ten different treatment sequences. The BOH availability of orally administered BDP was approximately 40% relative to inhaled HFA BDP. In addition, the fraction of an oral dose that reaches the systemic circulation was estimated from the 40% relative availability and previous lung deposition data to be 0.26. These estimated pharmacokinetic parameters will be used in the future to further characterize the pharmacokinetics of inhaled BDP and to compare the performance of different MDI products.

摘要

3M公司已使用推进剂HFA-134a(HFA)配制出一种新型无氯氟烃(不含CFC)的丙酸倍氯米松(BDP)定量吸入器(MDI)。肺部沉积研究表明,HFA BDP MDI可将约56%的BDP剂量(适配器外)输送至肺部,这一比例显著高于传统含CFC的BDP MDI所输送的5%-30%。随着用于定量吸入性皮质类固醇全身水平的新型灵敏生物分析方法不断涌现,药代动力学评估正成为灵敏且可重复的方法,可作为对肺部沉积研究所得数据的补充,用于评估和比较MDI的性能。本研究旨在确定口服BDP相对于吸入HFA BDP的倍氯米松(BOH)可用性,作为未来进行MDI产品比较的第一步。40名轻度哮喘患者完成了这项开放标签、随机、单剂量、两期交叉研究。每位患者在一个时期接受口服BDP剂量(0.2、0.5、1、2或5毫克),在另一个时期接受吸入BDP剂量(0.2或0.8毫克),10种不同治疗顺序各分配4名患者。口服BDP的BOH可用性相对于吸入HFA BDP约为40%。此外,根据40%的相对可用性和先前的肺部沉积数据估计,口服剂量中进入体循环的部分为0.26。这些估计的药代动力学参数将在未来用于进一步表征吸入BDP的药代动力学,并比较不同MDI产品的性能。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验