Department of Pharmaceutics and Biopharmaceutics, Kiel University, Grasweg 9a, 24118 Kiel, Germany.
Merck KGaA, Frankfurter Straße 250, 64293 Darmstadt, Germany.
Int J Pharm. 2020 Aug 30;586:119592. doi: 10.1016/j.ijpharm.2020.119592. Epub 2020 Jul 2.
Typically, smooth lactose particles are used as carrier in dry powder formulations for inhalation. Two classical approaches to improve their aerodynamic behaviour are the addition of fines (milled lactose) or magnesium stearate (MgSt). Mannitol (Parteck® M DPI) as an alternative carrier was used in this study. It has an irregular particle size distribution and a large and rough surface. This could be challenging for the detachment of micronised drug upon inhalation and it is unclear whether classic strategies for the optimisation of aerodynamic performance can be applied. In contrast, its rough surface could be an advantage in terms of drug load. To address these questions, the mannitol carrier was blended with two different drugs using various concentrations up to 50%. Self-produced mannitol fines and MgSt in different amounts and in combination were added. Blends were investigated regarding their in vitro aerodynamic performance, dosing behaviour and powder rheology. An addition of up to 30% drug load was possible while retaining good flowability and constant dosing behaviour. Despite the rough and indented carrier surface of the mannitol carrier, the addition of fines or MgSt increased the inhalable fraction, but higher concentrations of fines, as used for lactose blends, were necessary.
通常情况下,在干粉吸入剂中,乳糖颗粒被用作载体。改善其空气动力学性能的两种经典方法是添加细粉(研磨乳糖)或硬脂酸镁(MgSt)。在这项研究中,甘露醇(Parteck® M DPI)作为替代载体被使用。甘露醇的粒径分布不规则,表面大而粗糙。这可能会对吸入时微米化药物的脱离造成挑战,并且不清楚是否可以应用经典的空气动力学性能优化策略。相比之下,其粗糙的表面在药物负载方面可能具有优势。为了解决这些问题,使用不同浓度(高达 50%)将甘露醇载体与两种不同的药物混合。添加了不同量的自制甘露醇细粉和 MgSt 以及它们的组合。研究了混合物的体外空气动力学性能、给药行为和粉末流变性。在保持良好流动性和恒定给药行为的同时,可以添加高达 30%的药物负荷。尽管甘露醇载体的表面粗糙且有凹痕,但添加细粉或 MgSt 可以增加可吸入部分,但需要更高浓度的细粉,如用于乳糖混合物的细粉。