Department of Industrial and Physical Pharmacy, College of Pharmacy, Purdue University, 575 Stadium Mall Drive, West Lafayette, Indiana, 47907-2091, USA.
Advanced Drug Delivery Group, Faculty of Pharmacy, The University of Sydney, Sydney, NSW, 2006, Australia.
AAPS J. 2016 Sep;18(5):1213-1224. doi: 10.1208/s12248-016-9934-x. Epub 2016 Jun 2.
Aerosolisation performance of hygroscopic particles of colistin could be compromised at elevated humidity due to increased capillary forces. Co-spray drying colistin with a hydrophobic drug is known to provide a protective coating on the composite particle surfaces against moisture-induced reduction in aerosolisation performance; however, the effects of component ratio on surface coating quality and powder aerosolisation at elevated relative humidities are unknown. In this study, we have systematically examined the effects of mass ratio of hydrophobic azithromycin on surface coating quality and aerosolisation performance of the co-spray dried composite particles. Four combination formulations with varying drug ratios were prepared by co-spray drying drug solutions. Both of the drugs in each combination formulation had similar in vitro deposition profiles, suggesting that each composite particle comprises two drugs in the designed mass ratio, which is supported by X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS) data. XPS and ToF-SIMS measurements also revealed that 50% by weight (or 35% by molecular fraction) of azithromycin in the formulation provided a near complete coating of 96.5% (molar fraction) on the composite particle surface, which is sufficient to prevent moisture-induced reduction in fine particle fraction (FPF)recovered and FPFemitted. Higher azithromycin content did not increase coating coverage, while contents of azithromycin lower than 20% w/w did not totally prevent the negative effects of humidity on aerosolisation performance. This study has highlighted that a critical amount of azithromycin is required to sufficiently coat the colistin particles for short-term protection against moisture.
由于毛细作用力的增加,黏菌素吸湿颗粒在高湿度环境下的空气动力学性能可能会受到影响。将黏菌素与疏水性药物共同喷雾干燥已知可以在复合颗粒表面提供一层保护性涂层,防止因水分导致空气动力学性能降低;然而,在高相对湿度下,成分比例对表面涂层质量和粉末空气动力学性能的影响尚不清楚。在这项研究中,我们系统地研究了疏水性阿奇霉素的质量比对共喷雾干燥复合颗粒表面涂层质量和空气动力学性能的影响。通过共喷雾干燥药物溶液制备了四个具有不同药物比例的组合配方。每个组合配方中的两种药物都具有相似的体外沉积曲线,表明每个复合颗粒都包含两种按设计质量比的药物,这得到了 X 射线光电子能谱 (XPS) 和飞行时间二次离子质谱 (ToF-SIMS) 数据的支持。XPS 和 ToF-SIMS 测量还表明,配方中 50%(或 35%的分子分数)的阿奇霉素提供了对复合颗粒表面 96.5%(摩尔分数)的近乎完全覆盖,足以防止因湿度引起的细颗粒分数(FPF)回收率和 FPF 发射量降低。更高的阿奇霉素含量不会增加涂层覆盖率,而低于 20%w/w 的阿奇霉素含量并不能完全防止湿度对空气动力学性能的负面影响。这项研究强调了需要有一个临界量的阿奇霉素来充分覆盖黏菌素颗粒,以提供短期的防潮保护。