Liu Chao-Yu, Chen Ying-Ru, Mu Hsuan-Yu, Huang Jen-Huang
Department of Chemical Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan.
ACS Biomater Sci Eng. 2025 Jan 13;11(1):682-691. doi: 10.1021/acsbiomaterials.4c01377. Epub 2024 Dec 1.
Inhaled therapy has become a crucial treatment option for respiratory diseases like asthma, cystic fibrosis, and chronic obstructive pulmonary disease (COPD), delivering drugs directly to bronchial and alveolar tissues. However, traditional static cell models, while valuable for studying pharmacokinetics (PK) and pharmacodynamics (PD), fall short in replicating the dynamic nature of physiological breathing. In this study, we present a breathing lung chip model that integrates a dynamic breathing mechanism with an air-liquid interface (ALI) culture environment to overcome these limitations. The platform replicates key aspects of lung physiology, including a functional airway interface, cyclic breathing motion, and medium circulation. Using the Calu-3 cell line to model airway epithelium, our experiments show that the incorporation of breathing motion significantly enhances the efficacy of inhaled drug delivery and cellular uptake, resulting in improved treatment outcomes compared to direct exposure of the drug. While further research is needed to explore its full potential, this platform holds promise for advancing inhaled drug screening and respiratory disease research.
吸入疗法已成为治疗哮喘、囊性纤维化和慢性阻塞性肺疾病(COPD)等呼吸道疾病的关键治疗选择,可将药物直接输送到支气管和肺泡组织。然而,传统的静态细胞模型虽然对研究药代动力学(PK)和药效学(PD)很有价值,但在复制生理呼吸的动态特性方面存在不足。在本研究中,我们提出了一种呼吸肺芯片模型,该模型将动态呼吸机制与气液界面(ALI)培养环境相结合,以克服这些局限性。该平台复制了肺生理学的关键方面,包括功能性气道界面、周期性呼吸运动和介质循环。使用Calu-3细胞系模拟气道上皮,我们的实验表明,加入呼吸运动会显著提高吸入药物递送和细胞摄取的效果,与直接给药相比,治疗效果更好。虽然还需要进一步研究以探索其全部潜力,但该平台有望推动吸入药物筛选和呼吸道疾病研究的发展。