Protein stability in pulmonary drug delivery via nebulization

被引:91
作者
Hertel, Sebastian P. [1 ]
Winter, Gerhard [1 ]
Friess, Wolfgang [1 ]
机构
[1] Univ Munich, Dept Pharm Pharmaceut Technol & Biopharmaceut, D-81377 Munich, Germany
关键词
Protein instability; Protein aggregation; Air liquid-interface; Nebulization; Aerosolization; Aerosol collection; Subvisible particles; Protein unfolding; IMMUNOGLOBULIN TRANSPORT PATHWAY; COLONY-STIMULATING FACTOR; METERED-DOSE INHALER; AIR-WATER-INTERFACE; RECOMBINANT HUMAN DEOXYRIBONUCLEASE; VIBRATING-MESH NEBULIZATION; CYSTIC-FIBROSIS PATIENTS; RENAL-CELL CARCINOMA; SPRAY-DRIED POWDERS; FC FUSION PROTEIN;
D O I
10.1016/j.addr.2014.10.003
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Protein inhalation is a delivery route which offers high potential for direct local lung application of proteins. Liquid formulations are usually available in early stages of biopharmaceutical development and nebulizers are the device of choice for atomization avoiding additional process steps like drying and enabling fast progression to clinical trials. While some proteins were proven to remain stable throughout aerosolization e.g. DNase, many biopharmaceuticals are more susceptible towards the stresses encountered during nebulization. The main reason for protein instability is unfolding and aggregation at the air-liquid interface, a problem which is of particular challenge in the case of ultrasound and jet nebulizers due to recirculation of much of the generated droplets. Surfactants are an important formulation component to protect the sensitive biomolecules. A second important challenge is warming of ultrasound and vibrating mesh devices, which can be overcome by overfilling, precooled solutions or cooling of the reservoir. Ultimately, formulation development has to go hand in hand with device evaluation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:79 / 94
页数:16
相关论文
共 208 条
[1]
Adjei AL., 1997, INHALATION DELIVERY
[2]
Agrawal A., 2011, J EPITHEL BIOL PHARM, V4, P1, DOI [10.2174/1875044301104010001, DOI 10.2174/1875044301104010001]
[3]
Agu RU, 2001, RESP RES, V2, P198
[4]
The effect of formulation excipients on protein stability and aerosol performance of spray-dried powders of a recombinant humanized anti-IgE monoclonal antibody [J].
Andya, JD ;
Maa, YF ;
Costantino, HR ;
Nguyen, PA ;
Dasovich, N ;
Sweeney, TD ;
Hsu, CC ;
Shire, SJ .
PHARMACEUTICAL RESEARCH, 1999, 16 (03) :350-358
[5]
[Anonymous], PULM WORLDW SAL
[6]
[Anonymous], 2007, PULMONARY DRUG DELIV
[7]
MECHANISM OF POLY(ETHYLENE GLYCOL) INTERACTION WITH PROTEINS [J].
ARAKAWA, T ;
TIMASHEFF, SN .
BIOCHEMISTRY, 1985, 24 (24) :6756-6762
[8]
Ultrasonic atomization: Effect of liquid phase properties [J].
Avvaru, B ;
Patil, MN ;
Gogate, PR ;
Pandit, AB .
ULTRASONICS, 2006, 44 (02) :146-158
[9]
Improved treatment response to dornase alfa in cystic fibrosis patients using controlled inhalation [J].
Bakker, E. M. ;
Volpi, S. ;
Salonini, E. ;
van der Wiel-Kooij, E. C. ;
Sintnicolaas, C. J. J. C. M. ;
Hop, W. C. J. ;
Assael, B. M. ;
Merkus, P. J. F. M. ;
Tiddens, H. A. W. M. .
EUROPEAN RESPIRATORY JOURNAL, 2011, 38 (06) :1328-1335
[10]
Balwani G., 2002, 29 ANN M CONTR REL S