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哮喘与慢性阻塞性肺疾病管理的进展:运用Modulite技术提供无氯氟烃吸入疗法。

Advances in asthma and COPD management: delivering CFC-free inhaled therapy using Modulite technology.

作者信息

Acerbi D, Brambilla G, Kottakis I

机构信息

Chiesi Farmaceutici S.p.A, Drug Metabolism and Pharmacokinetics, Via Palermo 26/A, 43100 Parma, Parma, Italy.

出版信息

Pulm Pharmacol Ther. 2007;20(3):290-303. doi: 10.1016/j.pupt.2006.05.005. Epub 2006 May 27.

DOI:10.1016/j.pupt.2006.05.005
PMID:16890465
Abstract

Inhaled corticosteroids (ICS) and long-acting beta-agonists (LABA) are currently used in the management of asthma and chronic obstructive pulmonary disease (COPD). Localized targeted delivery of these drugs into the lungs is achieved by means of two types of inhalation devices; pressurized metered-dose inhalers (pMDIs) and dry powder-inhalers (DPIs). For environmental reasons, the chlorofluorocarbon (CFC) propellants used in pMDIs are now being replaced by ozone friendly hydrofluoroalkanes (HFAs). These new generation HFA-based pMDIs, developed to provide effective lung deposition of the active moiety, have a favorable safety and tolerability profile. However, HFA-based re-formulation of LABAs and ICS for pMDIs presents particular technical difficulties, especially in terms of ensuring dose content uniformity. This review focuses on the technology and clinical efficacy of the HFA solution pMDIs using Modulite platform technology (Chiesi Farmaceutici S.p.A). Modulite technology allows the development of HFA solution formulations that can mimic the established CFC-based drug formulations on a microgram to microgram basis and provides formulations with novel particle size distributions that improve on existing delivery systems; by manipulation of aerosol clouds and particle size, the delivery of HFA-formulated drugs can be optimized to either achieve fine particle fractions and deposition patterns similar to established CFC-based drug formulations, thus facilitating the transition to new environment-friendly pMDIs in the clinical setting, or achieve finer drug particles able to penetrate deeper into the bronchi for targeted drug delivery as medical need may dictate. Long-term, multiple-dose clinical studies of Modulite formulations of beclomethasone dipropionate (BDP), budesonide and formoterol have been demonstrated to be therapeutically equivalent to their respective previously established CFC or DPI formulations. As a result, a number of Modulite pMDIs have either recently gained regulatory approval in several European countries, or have completed clinical trials and are in the regulatory submission phase. Availability, in pMDI form, of drugs like formoterol, ICSs, and ICS/LABA combinations, all central to the effective management of asthma and COPD, is therefore expected to impact positively in assuring the continued availability of vital treatment options to patients and physicians.

摘要

吸入性糖皮质激素(ICS)和长效β受体激动剂(LABA)目前用于哮喘和慢性阻塞性肺疾病(COPD)的治疗。这些药物通过两种吸入装置实现肺部局部靶向给药;压力定量吸入器(pMDI)和干粉吸入器(DPI)。出于环境原因,pMDI中使用的氯氟烃(CFC)推进剂现在正被对臭氧友好的氢氟烷烃(HFA)所取代。这些新一代基于HFA的pMDI旨在使活性成分有效沉积于肺部,具有良好的安全性和耐受性。然而,将LABA和ICS重新配方为基于HFA的pMDI存在特殊技术难题,尤其是在确保剂量含量均匀性方面。本综述聚焦于使用Modulite平台技术(奇西制药公司)的HFA溶液pMDI的技术和临床疗效。Modulite技术能够开发出基于HFA的溶液制剂,可在微克到微克的基础上模拟已有的基于CFC的药物制剂,并提供具有新型粒度分布的制剂,改进现有给药系统;通过控制气溶胶云团和颗粒大小,基于HFA的药物递送可得到优化,要么实现与已有的基于CFC的药物制剂相似的细颗粒分数和沉积模式,从而便于在临床环境中向新型环保pMDI过渡,要么根据医疗需求实现更细的药物颗粒,能够更深入地穿透支气管以实现靶向给药。倍氯米松二丙酸酯(BDP)、布地奈德和福莫特罗的Modulite制剂的长期多剂量临床研究已证明在治疗上等同于各自先前已确立的CFC或DPI制剂。因此,一些Modulite pMDI最近在几个欧洲国家获得了监管批准,或者已完成临床试验并处于监管申报阶段。福莫特罗、ICS以及ICS/LABA组合等对哮喘和COPD有效管理至关重要的药物以pMDI形式可得,有望对确保患者和医生持续获得重要治疗选择产生积极影响。

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