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Challenges and advances in the development of inhalable drug formulations for cystic fibrosis lung disease
被引:22
|作者:
Ibrahim, Basma M.
[1
]
Tsifansky, Michael D.
[2
,3
]
Yang, Yan
[4
]
Yeo, Yoon
[1
,5
]
机构:
[1] Purdue Univ, Coll Pharm, Dept Ind & Phys Pharm, W Lafayette, IN 47907 USA
[2] Lutheran Gen Childrens Hosp, Dept Pediat, Div Pediat Crit Care Med, Park Ridge, IL 60068 USA
[3] Lutheran Gen Childrens Hosp, Dept Pediat, Div Pediat Pulmonol, Park Ridge, IL 60068 USA
[4] Jilin Univ, Coll Life Sci, Res Ctr Drug Metab, Changchun 130021, Peoples R China
[5] Purdue Univ, Weldon Sch Biomed Engn, W Lafayette, IN 47907 USA
关键词:
TRANSMEMBRANE CONDUCTANCE REGULATOR;
DRY POWDER INHALATION;
LIPOSOME-ENCAPSULATED TOBRAMYCIN;
OUTER-MEMBRANE PERMEABILITY;
INHALED HYPERTONIC SALINE;
MEDIATED GENE-TRANSFER;
AIRWAY SURFACE LIQUID;
ION-TRANSPORT DEFECT;
PSEUDOMONAS-AERUGINOSA;
IN-VITRO;
D O I:
10.1517/17425247.2011.561310
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Areas covered: This review discusses current and emerging therapeutic agents for CF therapy, selected physiological challenges to effective inhalational medication delivery, and various approaches to overcoming these challenges. The reader will find an integrated view of the known inhalational drug delivery challenges and the rationales for recent investigational inhalational drug formulations. Expert opinion: An ideal drug/gene delivery system to CF airways should overcome the tenacious sputum, which presents physical, chemical and biological barriers to effective transport of therapeutic agents to the targets and various cellular challenges.
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页码:451 / 466
页数:16
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