Fundamentals of pulmonary drug delivery

被引:199
作者
Groneberg, DA
Witt, C
Wagner, U
Chung, KF
Fischer, A
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Thorac Med, Natl Heart & Lung Inst, London SW3 6LY, England
[2] Humboldt Univ, Charite Sch Med, Dept Pediat Pneumol & Immunol, Berlin, Germany
[3] Humboldt Univ, Charite Sch Med, Dept Med, Berlin, Germany
[4] Univ Marburg, Sch Med, Dept Med, Marburg, Germany
关键词
airways; drug; aerosol; transport;
D O I
10.1053/rmed.2002.1457
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aerosol administration of peptide-based drugs plays an important role in the treatment of pulmonary and systemic diseases and the unique cellular properties of airway epithelium offers a great potential to deliver new compounds. As the relative contributions from the large airways to the alveolar space are important to the local and systemic availability, the sites and mechanism of uptake and transport of different target compounds have to be characterized. Among the different respiratory cells, the ciliated epithelial cells of the larger and smaller airways and the type I and type 11 pneumocytes are the key players in pulmonary drug transport. With their diverse cellular characteristics, each of these cell types displays a unique uptake possibility. Next to the knowledge of these cellular aspects, the nature of aerosolized drugs, characteristics of delivery systems and the depositional and pulmonary clearance mechanisms display major targets to optimize pulmonary drug delivery Based on the growing knowledge on pulmonary cell biology and pathophysiology due to modern methods of molecular biology, the future characterization of pulmonary drug transport pathways can lead to new strategies in aerosol drug therapy. (C) 2003 Elsevier Science Ltd All rights reserved.
引用
收藏
页码:382 / 387
页数:6
相关论文
共 64 条
[11]  
GIL J, 1983, FED PROC, V42, P2414
[12]   Expression of respiratory mucins in fatal status asthmaticus and mild asthma [J].
Groneberg, DA ;
Eynott, PR ;
Lim, S ;
Oates, T ;
Wu, R ;
Carlstedt, I ;
Roberts, P ;
McCann, B ;
Nicholson, AG ;
Harrison, BD ;
Chung, KF .
HISTOPATHOLOGY, 2002, 40 (04) :367-373
[13]   Expression of MUC5AC and MUC5B mucins in normal and cystic fibrosis lung [J].
Groneberg, DA ;
Eynott, PR ;
Oates, T ;
Lim, S ;
Wu, R ;
Carlstedt, I ;
Nicholson, AG ;
Chung, KF .
RESPIRATORY MEDICINE, 2002, 96 (02) :81-86
[14]   Distribution and function of the peptide transporter PEPT2 in normal and cystic fibrosis human lung [J].
Groneberg, DA ;
Eynott, PR ;
Döring, F ;
Dinh, QT ;
Oates, T ;
Barnes, PJ ;
Chung, KF ;
Daniel, H ;
Fischer, A .
THORAX, 2002, 57 (01) :55-60
[15]   Peptide transport in the mammary gland:: expression and distribution of PEPT2 mRNA and protein [J].
Groneberg, DA ;
Döring, F ;
Theis, S ;
Nickolaus, M ;
Fischer, A ;
Daniel, H .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2002, 282 (05) :E1172-E1179
[16]   Intestinal peptide transport:: ex vivo uptake studies and localization of peptide carrier PEPT1 [J].
Groneberg, DA ;
Döring, F ;
Eynott, PR ;
Fischer, A ;
Daniel, H .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2001, 281 (03) :G697-G704
[17]   Localization of the peptide transporter PEPT2 in the lung -: Implications for pulmonary oligopeptide uptake [J].
Groneberg, DA ;
Nickolaus, M ;
Springer, J ;
Döring, F ;
Daniel, H ;
Fischer, A .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (02) :707-714
[18]   BEHAVIOR OF HYGROSCOPIC PHARMACEUTICAL AEROSOLS AND THE INFLUENCE OF HYDROPHOBIC ADDITIVES [J].
HICKEY, AJ ;
MARTONEN, TB .
PHARMACEUTICAL RESEARCH, 1993, 10 (01) :1-7
[19]  
HIRAI KI, 1986, J ELECTRON MICROSC, V35, P19
[20]  
Holma B, 1967, Acta Med Scand Suppl, V473, P1