Biopharmaceutics and Pharmaceutical Technology, Saarland University, Saarbrücken, Germany.
Eur J Pharm Biopharm. 2011 Jan;77(1):132-8. doi: 10.1016/j.ejpb.2010.10.003. Epub 2010 Oct 14.
Absorption studies with aerosol formulation delivered by metered dose inhalers across cell- and tissue-based in vitro models of the pulmonary epithelia are not trivial due to the complexity of the processes involved: (i) aerosol generation and deposition, (ii) drug release from the carrier, and (iii) absorption across the epithelial air-blood barrier. In contrast to the intestinal mucosa, pulmonary epithelia are only covered by a thin film of lining fluid. Submersed cell culture systems would not allow to studying the deposition of aerosol particles and their effects on this delicate epithelial tissue. We developed a new Pharmaceutical Aerosol Deposition Device on Cell Cultures (PADDOCC) to mimic the inhalation of a single metered aerosol dose and its subsequent deposition on filter-grown pulmonary epithelial cell monolayers exposed to an air-liquid interface. The reproducibility of deposition of these dry powder aerosols and subsequent drug transport across Calu-3 monolayers with commercially available dry powder inhalers containing salbutamol sulphate or budesonide could be demonstrated. In the context of developing new dry powder aerosol formulations, PADDOCC appears as a useful tool, allowing reducing animal testing and faster translation into clinical trials.
由于涉及的过程复杂,通过计量吸入器输送的气溶胶制剂在肺上皮细胞和组织体外模型中的吸收研究并不简单:(i)气溶胶的生成和沉积,(ii)载体中药物的释放,以及(iii)穿过上皮空气-血液屏障的吸收。与肠道黏膜不同,肺上皮细胞仅被一层薄薄的衬里液覆盖。浸没细胞培养系统将无法研究气溶胶颗粒的沉积及其对这种脆弱的上皮组织的影响。我们开发了一种新的细胞培养药物气溶胶沉积装置(PADDOCC),以模拟单次计量吸入器剂量的吸入及其随后沉积在暴露于气液界面的滤过培养肺上皮细胞单层上。可以证明这些干粉气溶胶的沉积重现性以及随后含有硫酸沙丁胺醇或布地奈德的市售干粉吸入器中药物穿过 Calu-3 单层的转运。在开发新的干粉气溶胶制剂的背景下,PADDOCC 似乎是一种有用的工具,可减少动物试验并更快地转化为临床试验。