Party Petra, Piszman Zsófia Ilona, Farkas Árpád, Ambrus Rita
Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Eötvös Street 6, 6720 Szeged, Hungary.
Centre for Energy Research, Hungarian Academy of Sciences, Konkoly-Thege Miklós Street 29-33, 1121 Budapest, Hungary.
Pharmaceutics. 2024 Nov 17;16(11):1465. doi: 10.3390/pharmaceutics16111465.
Cystic fibrosis is a hereditary disease, which causes the accumulation of dense mucus in the lungs accompanied by frequent local inflammation. The non-steroidal anti-inflammatory drug ibuprofen (IBU) and the mucolytic mannitol (MAN) can treat these symptoms. Compared to per os administration, a lower dose of these drugs is sufficient to achieve the desired effect by delivering them in a pulmonary manner. However, it is still a challenge to administer high drug doses to the lungs. We aim to develop two inhaled powder formulations, a single-drug product of MAN and a combined formulation containing IBU and MAN. MAN was dissolved in an aqueous solution of Poloxamer-188 (POL). In the case of the combined formulation, a suspension was first prepared in a planetary mill via wet milling in POL medium. After the addition of leucine (LEU), the formulations were spray-dried. The prepared DPI samples were analyzed by using laser diffraction, scanning electron microscopy, powder X-ray diffraction, differential scanning calorimetry, density tests, in vitro aerodynamic studies (Andersen Cascade Impactor, Spraytec device), in vitro dissolution tests in artificial lung fluid, and in silico tests with stochastic lung model. The DPIs showed suitability for inhalation with low-density spherical particles of appropriate size. The LEU-containing systems were characterized by high lung deposition and adequate aerodynamic diameter. The amorphization during the procedures resulted in rapid drug release. We have successfully produced a single-drug formulation and an innovative combination formulation, which could provide complex treatment for patients with cystic fibrosis to improve their quality of life.
囊性纤维化是一种遗传性疾病,会导致肺部积聚浓稠黏液并伴有频繁的局部炎症。非甾体抗炎药布洛芬(IBU)和黏液溶解剂甘露醇(MAN)可以治疗这些症状。与口服给药相比,通过肺部给药的方式,较低剂量的这些药物就足以达到预期效果。然而,向肺部输送高剂量药物仍然是一项挑战。我们的目标是开发两种吸入粉剂配方,一种是甘露醇单药产品,另一种是含有布洛芬和甘露醇的复方制剂。甘露醇溶解于泊洛沙姆-188(POL)的水溶液中。对于复方制剂,首先在行星式球磨机中于POL介质中通过湿磨制备悬浮液。加入亮氨酸(LEU)后,将制剂进行喷雾干燥。通过激光衍射、扫描电子显微镜、粉末X射线衍射、差示扫描量热法、密度测试、体外空气动力学研究(安德森撞击器、Spraytec装置)、在人工肺液中的体外溶出试验以及使用随机肺模型的计算机模拟试验对制备的干粉吸入剂样品进行分析。干粉吸入剂显示出适合吸入,具有大小合适的低密度球形颗粒。含亮氨酸的体系具有高肺部沉积率和合适的空气动力学直径。制备过程中的非晶化导致药物快速释放。我们成功制备了一种单药制剂和一种创新的复方制剂,可为囊性纤维化患者提供综合治疗,以提高他们的生活质量。