Development of an In Vitro System to Study the Interactions of Aerosolized Drugs with Pulmonary Mucus

被引:10
作者
Alqahtani, Safar [1 ,2 ]
Roberts, Clive J. [1 ]
Stolnik, Snjezana [1 ]
Bosquillon, Cynthia [1 ]
机构
[1] Univ Nottingham, Sch Pharm, Nottingham NG7 2RD, England
[2] Prince Sattam bin Abdul Aziz Univ, Coll Pharm, Pharmaceut Chem Dept, Al Kharj 11942, Saudi Arabia
关键词
pulmonary delivery; aerosols; mucus; absorption; in vitro models; ORGANIC CATION TRANSPORTERS; RHEOLOGICAL PROPERTIES; CELL-LAYERS; DIFFUSION; PERMEATION; NANOPARTICLES; DELIVERY;
D O I
10.3390/pharmaceutics12020145
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mucus is the first biological component inhaled drugs encounter on their journey towards their pharmacological target in the upper airways. Yet, how mucus may influence drug disposition and efficacy in the lungs has been essentially overlooked. In this study, a simple in vitro system was developed to investigate the factors promoting drug interactions with airway mucus in physiologically relevant conditions. Thin layers of porcine tracheal mucus were prepared in Transwell(R) inserts and initially, the diffusion of various fluorescent dyes across those layers was monitored over time. A deposition system featuring a MicroSprayer(R) aerosolizer was optimized to reproducibly deliver liquid aerosols to multiple air-facing layers and then exploited to compare the impact of airway mucus on the transport of inhaled bronchodilators. Both the dyes and drugs tested were distinctly hindered by mucus with high logP compounds being the most affected. The diffusion rate of the bronchodilators across the layers was in the order: ipratropium approximate to glycopyronnium > formoterol > salbutamol > indacaterol, suggesting hydrophobicity plays an important role in their binding to mucus but is not the unique parameter involved. Testing of larger series of compounds would nevertheless be necessary to better understand the interactions of inhaled drugs with airway mucus.
引用
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页数:15
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