Petra Party, Zsófia Ilona Piszman, Árpád Farkas, Rita Ambrus
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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<sup>®</sup> device), in vitro dissolution tests in artificial lung fluid, and in silico tests with stochastic lung model. <b>Results:</b> 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. 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引用次数: 0
摘要
背景:囊性纤维化是一种遗传性疾病,会导致肺部积聚大量粘液,并伴有频繁的局部炎症。非甾体抗炎药布洛芬(IBU)和粘液溶解剂甘露醇(MAN)可治疗这些症状。与经口给药相比,通过肺部给药,只需较低剂量就能达到预期效果。然而,向肺部输送高剂量药物仍是一项挑战。我们的目标是开发两种吸入粉末制剂,一种是 MAN 单药产品,另一种是含有 IBU 和 MAN 的复合制剂。方法:将 MAN 溶解在 Poloxamer-188 (POL) 的水溶液中。在混合制剂中,首先在行星研磨机中通过在 POL 介质中进行湿研磨制备悬浮液。加入亮氨酸(LEU)后,对配方进行喷雾干燥。制备的 DPI 样品通过激光衍射、扫描电子显微镜、粉末 X 射线衍射、差示扫描量热仪、密度测试、体外空气动力学研究(Andersen Cascade Impactor、Spraytec® 设备)、人工肺液体外溶解测试以及随机肺模型的硅学测试进行了分析。结果显示结果表明,DPIs 适合吸入适当大小的低密度球形颗粒。含 LEU 系统的特点是高肺沉积和适当的空气动力学直径。操作过程中的非晶化作用导致药物快速释放。结论:我们已成功制备出一种单药制剂和一种创新的复合制剂,可为囊性纤维化患者提供复合治疗,改善他们的生活质量。
Comprehensive In Vitro and In Silico Aerodynamic Analysis of High-Dose Ibuprofen- and Mannitol-Containing Dry Powder Inhalers for the Treatment of Cystic Fibrosis.
Background: 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. Methods: 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. Results: 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. Conclusions: 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.
PharmaceuticsPharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍:
Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications, and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.