Institute of Pharmaceutical Science, Faculty of Life Sciences and Medicine, King's College London, London, UK.
Drug Metabolism and Pharmacokinetics, Research and Early Development, Respiratory and Immunology (R&I), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
Expert Opin Drug Metab Toxicol. 2021 May;17(5):611-625. doi: 10.1080/17425255.2021.1908262. Epub 2021 Apr 21.
The lungs possess many xenobiotic metabolizing enzymes which influence the pharmacokinetics and safety of inhaled medicines. Anticipating metabolism in the lungs provides an opportunity to optimize new inhaled medicines and overcome challenges in their development.
This article summarizes current knowledge on xenobiotic metabolizing enzymes in the lungs. The impact of metabolism on inhaled medicines is considered with examples of how this impacts small molecules, biologics and macromolecular formulation excipients. Methods for measuring and predicting xenobiotic lung metabolism are critically reviewed and the potential for metabolism to influence inhalation toxicology is acknowledged.
Drugs can be optimized by molecular modification to (i) reduce systemic exposure using a 'soft drug' approach, (ii) improve bioavailability by resisting metabolism, or (iii) use a prodrug approach to overcome pharmacokinetic limitations. Drugs that are very labile in the lungs may require a protective formulation. Some drug carriers being investigated for PK-modification rely on lung enzymes to trigger drug release or biodegrade. Lung enzyme activity varies with age, race, smoking status, diet, drug exposure and preexisting lung disease. New experimental technologies to study lung metabolism include tissue engineered models, improved analytical capability and models.
肺部拥有许多影响吸入药物药代动力学和安全性的外源代谢酶。预测肺部的代谢情况为优化新型吸入药物提供了机会,并克服了其开发过程中的挑战。
本文总结了肺部外源代谢酶的现有知识。本文考虑了代谢对外源药物的影响,并举例说明了这如何影响小分子、生物制剂和大分子制剂辅料。本文还批判性地回顾了测量和预测肺部外源代谢的方法,并承认了代谢对吸入毒理学的潜在影响。
可以通过分子修饰来优化药物:(i)采用“软药”方法降低全身暴露,(ii)通过抵抗代谢来提高生物利用度,或(iii)采用前药方法克服药代动力学限制。在肺部非常不稳定的药物可能需要保护制剂。一些正在研究用于 PK 修饰的药物载体依赖于肺部酶来触发药物释放或生物降解。肺部酶的活性随年龄、种族、吸烟状况、饮食、药物暴露和预先存在的肺部疾病而变化。研究肺部代谢的新技术包括组织工程模型、改进的分析能力和模型。