Leach C L, Davidson P J, Boudreau R J
3M Pharmaceuticals, ST Paul, MN 55144-1000, USA.
Eur Respir J. 1998 Dec;12(6):1346-53. doi: 10.1183/09031936.98.12061346.
Hydrofluoroalkane-134a (HFA) beclomethasone dipropionate (BDP) was formulated in a metered-dose inhaler (MDI) to deliver a particle size of 1.1 microm compared with 35 microns for currently marketed chlorofluorocarbon (CFC)-BDP products. Two phase I single-dose human deposition studies were conducted using technetium 99m-radiolabelled BDP in a press-and-breathe actuator without an add-on spacer. A healthy volunteer study (n=6) showed that 55-60% of the HFA-BDP ex-actuator dose was deposited in the lungs, with 29-30% deposited in the oropharynx. CFC-BDP deposition was 4-7% in the lungs and 90-94% in the oropharynx. The pattern of deposition within the lung showed that HFA-BDP was spread diffusely throughout the lung airways, whereas CFC-BDP was confined to the central airways with little, if any, peripheral airway deposition. A second study with asthmatics (n=16) confirmed that 56% of the HFA-BDP dose was deposited in the airways, with 33% in the oropharynx. In conclusion, hydrofluoroalkane-134a-beclomethasone dipropionate deposition was much greater in the airways than chlorofluorocarbon-beclomethasone dipropionate, with a concomitant reduction in oropharyngeal deposition. The increased lung deposition efficiency of the hydrofluoroalkane propellant has led to a reduction in the amount of beclomethasone dipropionate needed to achieve a similar efficacy. The penetration of the hydrofluoroalkane to the small airways may provide asthma treatment not afforded by conventional chlorofluorocarbons.
将丙酸倍氯米松(BDP)制成含氢氟烷烃-134a(HFA)的定量吸入器(MDI),其递送的颗粒大小为1.1微米,而目前市售的含氯氟烃(CFC)-BDP产品的颗粒大小为35微米。使用99m锝标记的BDP在无附加储雾罐的按压式吸入装置中进行了两项I期单剂量人体沉积研究。一项健康志愿者研究(n = 6)表明,HFA-BDP从吸入装置喷出后的剂量有55 - 60%沉积在肺部,29 - 30%沉积在口咽部。CFC-BDP在肺部的沉积率为4 - 7%,在口咽部为90 - 94%。肺部的沉积模式显示,HFA-BDP在整个肺气道中呈弥漫性分布,而CFC-BDP则局限于中央气道,外周气道几乎没有沉积(如果有也是极少的)。另一项针对哮喘患者的研究(n = 16)证实,HFA-BDP剂量的56%沉积在气道,33%沉积在口咽部。总之,与含氯氟烃-丙酸倍氯米松相比,氢氟烷烃-134a-丙酸倍氯米松在气道中的沉积要多得多,同时口咽部沉积减少。氢氟烷烃推进剂肺部沉积效率的提高导致达到相似疗效所需的丙酸倍氯米松量减少。氢氟烷烃向小气道的渗透可能提供传统含氯氟烃无法实现的哮喘治疗效果。