School of Pharmacy, University of Nottingham, University Park, Nottingham NG7 2RD, United Kingdom.
GlaxoSmithKline, David Jack R&D Centre, Park Road, Ware SG12 0DP, Hertfordshire, United Kingdom.
Eur J Pharm Biopharm. 2019 Aug;141:210-220. doi: 10.1016/j.ejpb.2019.05.022. Epub 2019 May 30.
Although the mucus layer is the first biological barrier encountered by inhaled drugs upon their deposition in the upper airways, its potential impact on drug dissolution and absorption in the lung has hardly been investigated. Bio-relevant in vitro models were therefore used to assess the role of airway mucus in the fate of drug particles at the air-epithelium interface. Salbutamol and indomethacin were used as model Biopharmaceutics Classification System (BCS) class III and class II drugs, respectively. Dry powders were reproducibly aerosolised using a PennCentury™ Dry Powder Insufflator onto multiple air-liquid interfaced layers of the broncho-epithelial cell line Calu-3 or thin layers of porcine tracheal mucus mounted onto Transwells inserts, as well as on empty Transwells. Comparison of the permeation profiles of the two drugs indicated that mucus acted as a barrier for salbutamol transport but increased that of indomethacin, suggesting it facilitates the dissolution of poorly soluble drugs. In presence of Calu-3 layers, the permeability of salbutamol was even more restricted while indomethacin transport was enhanced further. This study demonstrates mucus distinctly affects the absorption characteristics of drugs with different physico-chemical properties. Hence, drug-mucus interactions should be considered during the development of inhaled drugs.
尽管黏液层是吸入药物在上呼吸道沉积时遇到的第一道生物屏障,但它对肺部药物溶解和吸收的潜在影响几乎没有被研究过。因此,使用生物相关的体外模型来评估气道黏液在药物颗粒在气-上皮界面的命运中的作用。沙丁胺醇和吲哚美辛分别用作生物药剂学分类系统 (BCS) 第三类和第二类药物的模型。使用 PennCentury™干粉分散器将干粉可重复地雾化到支气管上皮细胞系 Calu-3 的多个气-液界面层上,或涂有多层猪气管黏液的 Transwell 插入物上,以及空 Transwell 上。两种药物的渗透曲线比较表明,黏液对沙丁胺醇的转运起屏障作用,但增加了吲哚美辛的转运,表明它有助于溶解难溶性药物。在存在 Calu-3 层的情况下,沙丁胺醇的渗透性受到更严格的限制,而吲哚美辛的转运则进一步增强。这项研究表明,黏液明显影响具有不同物理化学性质的药物的吸收特性。因此,在开发吸入药物时应考虑药物-黏液相互作用。