Drug metabolism in the lungs: opportunities for optimising inhaled medicines

被引:34
|
作者
Enlo-Scott, Zachary [1 ]
Backstrom, Erica [2 ]
Mudway, Ian [3 ,4 ,5 ]
Forbes, Ben [1 ]
机构
[1] Kings Coll London, Fac Life Sci & Med, Inst Pharmaceut Sci, London, England
[2] AstraZeneca, Drug Metab & Pharmacokinet, Res & Early Dev, Resp & Immunol R&I,BioPharmaceut R&D, Gothenburg, Sweden
[3] Imperial Coll London, MRC Ctr Environm & Hlth, Sch Populat Hlth & Environm Sci, London, England
[4] Imperial Coll London, Natl Inst Hlth Res, Hlth Protect Res Unit Chem & Radiat Threats & Haz, London, England
[5] Imperial Coll London, Natl Inst Hlth Res, Hlth Protect Res Unit Environm Exposures & Hlth, London, England
关键词
Respiratory; pulmonary; drug metabolism; lung metabolism; inhaled drugs; pharmacokinetics; inhalation toxicology; pro-drug; soft drug; FLUTICASONE PROPIONATE; PROTEASE INHIBITORS; PULMONARY; EXPRESSION; PHARMACOKINETICS; CICLESONIDE; ROFLUMILAST; ABSORPTION; CALCITONIN; DELIVERY;
D O I
10.1080/17425255.2021.1908262
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction 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. Areas covered 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. Expert opinion 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 in silico models.
引用
收藏
页码:611 / 625
页数:15
相关论文
共 50 条
  • [31] Drug Metabolism and Pharmacokinetics of Nanodrugs from Chinese Medicines and Natural Products
    Liu, Chang-Xiao
    Si, Duan-Yun
    Xiao, Xue-Feng
    He, Xin
    Li, Ya-Zhuo
    CURRENT DRUG METABOLISM, 2012, 13 (05) : 659 - 666
  • [32] Optimising proteolysis-targeting chimeras (PROTACs) for oral drug delivery: a drug metabolism and pharmacokinetics perspective
    Pike, Andy
    Williamson, Beth
    Harlfinger, Stephanie
    Martin, Scott
    McGinnity, Dermot F.
    DRUG DISCOVERY TODAY, 2020, 25 (10) : 1793 - 1800
  • [33] Carboxylesterase inhibitors from clinically available medicines and their impact on drug metabolism
    Song, Yun-Qing
    Jin, Qiang
    Wang, Dan-Dan
    Hou, Jie
    Zou, Li-Wei
    Ge, Guang-Bo
    CHEMICO-BIOLOGICAL INTERACTIONS, 2021, 345
  • [34] The pivotal role of drug metabolism and pharmacokinetics in the discovery and development of new medicines
    Alavijeh, MS
    Palmer, AM
    IDRUGS, 2004, 7 (08) : 755 - 763
  • [35] Multimodal imaging of drug and excipients in rat lungs following an inhaled administration of controlled-release drug laden PLGA microparticles
    Robinson, Eve
    Giffen, Paul
    Hassall, Dave
    Ball, Doug
    Reid, Heather
    Coe, Diane
    Teague, Simon
    Terry, Rebecca
    Earl, Meredith
    Marchand, Joseph
    Farrer, Brian
    Havelund, Rasmus
    Gilmore, Ian S.
    Marshall, Peter S.
    ANALYST, 2021, 146 (10) : 3378 - 3390
  • [36] Liver X receptors in lipid metabolism: opportunities for drug discovery
    Cynthia Hong
    Peter Tontonoz
    Nature Reviews Drug Discovery, 2014, 13 : 433 - 444
  • [37] Optimising inhaled mannitol for cystic fibrosis in an adult population
    Flume, Patrick A.
    Aitken, Moira L.
    Bilton, Diana
    Agent, Penny
    Charlton, Brett
    Forster, Emma
    Fox, Howard G.
    Hebestreit, Helge
    Kolbe, John
    Zuckerman, Jonathan B.
    Button, Brenda M.
    BREATHE, 2015, 11 (01) : 39 - 48
  • [38] Liver X receptors in lipid metabolism: opportunities for drug discovery
    Hong, Cynthia
    Tontonoz, Peter
    NATURE REVIEWS DRUG DISCOVERY, 2014, 13 (06) : 433 - 444
  • [39] Understanding the mechanisms controlling inhaled drug retention in the lungs using human bronchial epithelial cell layers
    Bosquillon, C.
    Panduga, V.
    Stocks, M. J.
    BRITISH JOURNAL OF PHARMACOLOGY, 2019, 176 (16) : 3009 - 3009
  • [40] UPTAKE BY THE LUNGS AND DISPOSITION OF INHALED TOBACCO STEROLS
    HOLDEN, WE
    MAIER, J
    LIEBLER, J
    MALINOW, MR
    CLINICAL RESEARCH, 1986, 34 (01): : A79 - A79