Department of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkhla, 90112, Thailand.
AAPS PharmSciTech. 2013 Dec;14(4):1294-302. doi: 10.1208/s12249-013-0024-4. Epub 2013 Aug 23.
The aim of the study was to investigate the factors affecting the stability and performance of ipratropium bromide and fenoterol hydrobromide in a pressurized-metered dose inhaler (pMDI). A factorial design was applied to investigate the effects of three parameters (propellant, water, and ethanol) on the performance of 27 designed formulations of a solution-based pMDI. The formulations that contained a hydrofluoroalkane (HFA) propellant lower than 72% v/v and an ethanol concentration higher than 27% v/v remained as clear solutions. Nine formulations that contained the HFA propellant higher than 74% v/v precipitated. The results indicated that it was not only the HFA propellant content of the formulations that was related to the formulation instability but also ethanol content. Only six formulations from the 18 formulations, that did not precipitate, produced drug contents that were within the acceptable range (80-120%). These six formulations generated aerosols with mass median aerodynamic diameters (MMAD) of approximately 2 μm with a fine particle fraction (FPF; particle size, <6.4 μm) between 45% and 52%. The MMAD and FPF did not change significantly after 6 months of storage (P > 0.05).
本研究旨在探讨影响定量吸入气雾剂(pMDI)中溴化异丙托品和盐酸芬特罗稳定性和性能的因素。采用析因设计考察了三种参数(推进剂、水和乙醇)对基于溶液的 pMDI 的 27 种设计配方的性能的影响。含有低于 72%v/v 的氢氟烷烃(HFA)推进剂和高于 27%v/v 的乙醇浓度的制剂仍保持为澄清溶液。含有高于 74%v/v 的 HFA 推进剂的 9 种制剂发生沉淀。结果表明,不仅是制剂中的 HFA 推进剂含量与制剂不稳定性有关,而且乙醇含量也是如此。在未沉淀的 18 种制剂中,仅有 6 种制剂产生的药物含量在可接受范围内(80-120%)。这 6 种制剂产生的气溶胶的质量中值空气动力学直径(MMAD)约为 2μm,细颗粒分数(FPF;粒径,<6.4μm)在 45%至 52%之间。在 6 个月的储存后,MMAD 和 FPF 没有显著变化(P>0.05)。