Developing inhaled protein therapeutics for lung diseases

被引:54
作者
Matthews, Abigail A. [1 ]
Ee, Pui Lai Rachel [2 ,3 ]
Ge, Ruowen [1 ]
机构
[1] Natl Univ Singapore, Fac Sci, Dept Biol Sci, 16 Sci Dr 4, Singapore 117558, Singapore
[2] Natl Univ Singapore, Dept Pharm, 18 Sci Dr 4, Singapore 117543, Singapore
[3] NUS Grad Sch Integrat Sci & Engn, 21 Lower Kent Ridge Rd, Singapore 119077, Singapore
来源
MOLECULAR BIOMEDICINE | 2020年 / 1卷 / 01期
关键词
Inhalation; Proteins; Biologics; Drug delivery; Lung diseases; DRUG-DELIVERY; CONFORMATIONAL STABILITY; POLYMERIC NANOPARTICLES; MONOCLONAL-ANTIBODY; PULMONARY DELIVERY; DNA NANOPARTICLES; AEROSOL THERAPY; MUCUS; NEBULIZATION; INHALATION;
D O I
10.1186/s43556-020-00014-z
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
Biologic therapeutics such as protein/polypeptide drugs are conventionally administered systemically via intravenous injection for the treatment of diseases including lung diseases, although this approach leads to low target site accumulation and the potential risk for systemic side effects. In comparison, topical delivery of protein drugs to the lung via inhalation is deemed to be a more effective approach for lung diseases, as proteins would directly reach the target in the lung while exhibiting poor diffusion into the systemic circulation, leading to higher lung drug retention and efficacy while minimising toxicity to other organs. This review examines the important considerations and challenges in designing an inhaled protein therapeutics for local lung delivery: the choice of inhalation device, structural changes affecting drug deposition in diseased lungs, clearance mechanisms affecting an inhaled protein drug's lung accumulation, protein stability, and immunogenicity. Possible approaches to overcoming these issues will also be discussed.
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页数:14
相关论文
共 104 条
[21]   Factors to consider when selecting a nebulizer for a new inhaled drug product development program [J].
Elphick, Mark ;
von Hollen, Dirk ;
Pritchard, John N. ;
Nikander, Kurt ;
Hardaker, Lucy E. A. ;
Hatley, Ross H. M. .
EXPERT OPINION ON DRUG DELIVERY, 2015, 12 (08) :1375-1387
[22]   Stability of urease during aerosolization: The effect of operating conditions [J].
Fangmark, I ;
Carpin, JC .
JOURNAL OF AEROSOL SCIENCE, 1998, 29 (03) :279-288
[23]  
Fangmark I., 1996, J AEROSOL SCI, V27, pS231
[24]   Inhaled protein/peptide-based therapies for respiratory disease [J].
Robert C. Fellner ;
Shawn T. Terryah ;
Robert Tarran .
Molecular and Cellular Pediatrics, 3 (1)
[25]   Preclinical models for pulmonary drug delivery [J].
Fernandes, Claudia A. ;
Vanbever, Rita .
EXPERT OPINION ON DRUG DELIVERY, 2009, 6 (11) :1231-1245
[26]   Immunogenicity of different stressed IgG monoclonal antibody formulations in immune tolerant transgenic mice [J].
Filipe, Vasco ;
Jiskoot, Wim ;
Basmeleh, Abdul Hafid ;
Halim, Andhyk ;
Schellekens, Huub ;
Brinks, Vera .
MABS, 2012, 4 (06) :740-752
[27]   Vibrating Mesh Nebulisation of Pro-Antimicrobial Peptides for Use in Cystic Fibrosis [J].
Forde, Eanna ;
Kelly, Graeme ;
Sweeney, Louise ;
Fitzgerald-Hughes, Deirdre ;
MacLoughlin, Ronan ;
Devocelle, Marc .
PHARMACEUTICS, 2019, 11 (05)
[28]  
Forier K, 2013, NANOMEDICINE-UK, V8, P935, DOI [10.2217/NNM.12.129, 10.2217/nnm.12.129]
[29]   PEGylation prolongs the pulmonary retention of an anti-IL-17A Fab' antibody fragment after pulmonary delivery in three different species [J].
Freches, Danielle ;
Patil, Harshad P. ;
Franco, Maria Machado ;
Uyttenhove, Catherine ;
Heywood, Sam ;
Vanbever, Rita .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2017, 521 (1-2) :120-129
[30]   Computational modeling of lung deposition of inhaled particles in chronic obstructive pulmonary disease (COPD) patients: identification of gaps in knowledge and data [J].
Ganguly, Koustav ;
Carlander, Ulrika ;
Garessus, Estella D. G. ;
Friden, Markus ;
Eriksson, Ulf G. ;
Tehler, Ulrika ;
Johanson, Gunnar .
CRITICAL REVIEWS IN TOXICOLOGY, 2019, 49 (02) :160-173